Expanding Virtual Screening Capabilities
DrTarget’s 2025 portfolio integrates over 500 new AI-powered virtual screening programs, leveraging data from 800+ PubChem bioassays. These programs enable the exploration of 2 million molecules across a diverse range of therapeutic areas, accelerating early-stage drug discovery.
Harnessing PubChem Data for Smarter Discovery
🔹 AI-enhanced lead optimization
🔹 Chemical property assessment for drug-likeness
🔹 Advanced computational workflows for novel targets
802 Pubchem assays support 576 machine learning projects associated to 249 diseases corresponding to 29 therapeutic areas. The assays involve > 400 different phenotypes and 461 genes.
See PubChem assays supporting machine learning programs clicking in the therapeutic area tabs.
Find drTarget portfolio details in table. Use scroll bar or search funtion to select specific therapeutic areas, molecular targets or phenotypes.
| area | disease | program | assayType | PubChemAssay | gene | testedComopunds | activeCompounds |
|---|---|---|---|---|---|---|---|
| antiBacterial | plague | Yersinia pestis | targetBased | YopH HTS | YopH | 139929 | 223 |
| psychiatricDisorder | schizophrenia | Wnt/Beta-catenin pathway | phenotypic | Wnt/Beta-catenin HTS Measured in Cell-Based System Using Plate Reader - 2161-01_Activator_SinglePoint_HTS_Activity | 304218 | 3630 | |
| biologicalProcess | geneRegulation | start codon recognition | phenotypic | Whole cell Yeast HTS to identify compounds modulating the fidelity of the start codon recognition in eukaryotes. Measured in Whole Organism System Using Plate Reader - 2155-01_Other_SinglePoint_HTS_Activity | 347159 | 450 | |
| gastroIntestinal | intestinal disease | RORC | targetBased | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | RORC | 304060 | 10600 |
| nervousSystem | neurodegeneration | Caspase6Inhibitors | targetBased | VEID(2) R110 Enzymatic Primary HTS to identify Inhibitors of Caspase 6 Measured in Biochemical System Using Plate Reader - 7052-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | CASP6 | 344318 | 1854 |
| nervousSystem | neurodegeneration | USP30 | targetBased | USP30 deubiquitinase inhibition: Primary qHTS | USP30 | 47480 | 2500 |
| nervousSystem | neurodegeneration | USP28 | targetBased | USP28 deubiquitinase inhibition: Primary qHTS | USP28 | 47480 | 1413 |
| immune | immunodeficiency disease | USP17L5 | targetBased | USP17 deubiquitinase inhibition: Primary qHTS | USP17L5 | 47480 | 3075 |
| USP10 | targetBased | USP10 deubiquitinase inhibition: Primary qHTS | USP10 | 47480 | 509 | ||
| cancer | neoplastic disease or syndrome | USP8 | targetBased | USP8 deubiquitinase inhibition: Primary qHTS | USP8 | 47480 | 2010 |
| immune | fibrosis | p47phoxInhibitors | targetBased | uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) | NCF1 | 217454 | 1142 |
| nervousSystem | neurodegeneration | MCL1 | targetBased | uHTS of Mcl-1/Noxa interaction inhibitors | MCL1 | 217330 | 3334 |
| nervousSystem | neurodegeneration | MCL1 | targetBased | uHTS of Mcl-1/Bid interaction inhibitors | MCL1 | 218602 | 2129 |
| SENP7 | targetBased | uHTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 7 (SENP7) | SENP7 | 331670 | 4902 | ||
| nervousSystem | neurodegeneration | SENP6 | targetBased | uHTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 6 (SENP6) | SENP6 | 330392 | 5817 |
| muculoEskeletalConnective | connective tissue disease | NLRP3 | targetBased | uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | 330392 | 1295 |
| biologicalProcess | alcalinePhosphatase | ALPI_inhibitors | targetBased | uHTS Luminescent assay for identification of inhibitors of mouse intestinal alkaline phosphatase | ALPI | 331670 | 664 |
| biologicalProcess | alcalinePhosphatase | ALPI_inhibitors | targetBased | uHTS Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase | ALPI | 330392 | 393 |
| metabolicEndocrine | cholesterolLevels | ALPI_activators | targetBased | uHTS Luminescent assay for identification of activators of mouse intestinal alkaline phosphatase | ALPI | 331670 | 785 |
| metabolicEndocrine | cholesterolLevels | ALPI_activators | targetBased | uHTS Luminescent assay for identification of activators of human intestinal alkaline phosphatase | ALPI | 330392 | 537 |
| immune | Crohn's disease | NOD2 | targetBased | uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | 292323 | 1836 |
| NOD1 | targetBased | uHTS luminescence assay for the identification of compounds that inhibit NOD1 | NOD1 | 289422 | 2997 | ||
| immune | immunomodulation | NFKB1_activation | phenotypic | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation | 330392 | 1733 | |
| immune | immunomodulation | NFKB1_activation | phenotypic | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation | 331670 | 1077 | |
| UBE2N | targetBased | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | UBE2N | 330393 | 1538 | ||
| muculoEskeletalConnective | boneDisease | ALPL_inhibitors | targetBased | uHTS identification of TNAP inhibitors in the absence of phosphate acceptor performed in luminescent assay | ALPL | 195560 | 517 |
| cancer | resistanecToRadiation | SUMO1 | targetBased | uHTS identification of SUMO1-mediated protein-protein interactions | SUMO1 | 363840 | 1202 |
| metabolicEndocrine | type I and type II diabetes | beta-cell replication | phenotypic | uHTS identification of small molecules that induce b-cell replication in the MIN-6 cell line | 330392 | 956 | |
| metabolicEndocrine | obesity, diabetes and hyperlipidemia | TriglycerideAccumulationInhibitors | phenotypic | uHTS identification of small molecule Triacylglycerol inhbitors in a fluoresence assay | 226721 | 1501 | |
| metabolicEndocrine | obesity, diabetes and hyperlipidemia | Rev-erb Alpha | phenotypic | uHTS identification of small molecule modulators of Rev-erb Alpha. | 371540 | 2956 | |
| nervousSystem | neurodegeneration | GRIN3A | targetBased | uHTS identification of small molecule modulators of NR3A | GRIN3A | 339772 | 8480 |
| cardioVascular | myocardial infarction | myocardial damage | phenotypic | uHTS identification of small molecule modulators of myocardial damage | 359244 | 2272 | |
| cancer | glioblastoma | inhibitors of TWEAK-Fn14 interactions | phenotypic | uHTS identification of small molecule inhibitors of TWEAK-Fn14 interactions, using a cell-based reporter assay | 362063 | 7302 | |
| TIM23 | targetBased | uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent assay | TIM23 | 331671 | 4405 | ||
| TIM10 | targetBased | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay | TIM10 | 331671 | 7319 | ||
| TIM10 | targetBased | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay | TIM10 | 331671 | 4615 | ||
| nervousSystem | neurodegeneration | mPTP | phenotypic | uHTS identification of small molecule inhibitors of the mitochondrial permeability transition pore via an absorbance assay | 363840 | 5033 | |
| nervousSystem | neurodegeneration | SENP1 | targetBased | uHTS identification of small molecule inhibitors of the catalytic domain of the SUMO protease, SENP1 in a FRET assay | SENP1 | 363840 | 774 |
| nervousSystem | neurodegeneration | PTPN5 | targetBased | uHTS identification of small molecule inhibitors of Striatal-Enriched Phosphatase via a fluorescence intensity assay | PTPN5 | 359244 | 887 |
| antiMicrobial | malaria | Plasmodium berghei | targetBased | uHTS identification of small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay | G6PD-6PGL | 348923 | 2710 |
| metabolicEndocrine | obesity associated insulin resistance and the metabolic syndrome | ACP1_inhibitors | targetBased | uHTS identification of small molecule inhibitors of Low Molecular Weight Protein Tyrosine Phosphatase, LMPTP, via a fluorescence intensity assay | ACP1 | 363840 | 817 |
| biologicalProcess | Ubiquitination | COPS5 | targetBased | uHTS identification of small molecule inhibitors of Csn-mediated Deneddylation of Cullin-Ring Ligases, vis a fluorescence polarization assay | COPS5 | 363840 | 1401 |
| cancer | acuteLymphoblasticLymphoma | artemis_inhibitors | targetBased | uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | DCLRE1C | 30104 | 235 |
| cancer | cancerGeneral | FASN_inhibitors | targetBased | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay | FASN | 362063 | 2427 |
| cancer | neoplastic disease or syndrome | OPRK1 | targetBased | uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | 290355 | 265 |
| GPR183 | targetBased | uHTS identification of small molecule antagonists of the EBI2 receptor via a luminescent beta-arrestin assay | GPR183 | 363840 | 2946 | ||
| cancer | metastasis | CCR6_antagonists | targetBased | uHTS identification of small molecule antagonists of the CCR6 receptor via a luminescent beta-arrestin assay | CCR6 | 340696 | 1654 |
| cancer | cancerGeneral | APLNR_antagonists | targetBased | uHTS identification of small molecule antagonists of the APJ receptor via a luminescent beta-arrestin assay | APLNR | 330392 | 1062 |
| cardioVascular | hypertension | APLNR_agonists | targetBased | uHTS identification of small molecule agonists of the APJ receptor via a luminescent beta-arrestin assay | APLNR | 330348 | 347 |
| cancer | cancerGeneral | PERK-elF2a-CHOP pathway activators | phenotypic | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay | 331671 | 1124 | |
| cytoprotection | cellRecovery | IRE1-XBP1 pathway activators | phenotypic | uHTS identification of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay | 331671 | 1099 | |
| LARGE | targetBased | uHTS identification of small molecule activators of alpha dystroglycan glycosylation | LARGE | 363840 | 805 | ||
| SKN-1 | targetBased | uHTS identification of SKN-1 Inhibitors in a fluoresence assay | SKN-1 | 363840 | 1794 | ||
| NRP1 | targetBased | uHTS identification of modulators of interaction between CendR and NRP-1 using Fluorescence Polarization assay | NRP1 | 363840 | 3086 | ||
| cancer | neoplastic disease or syndrome | PABPC1 | targetBased | uHTS identification of microRNA-mediated mRNA deadenylation inhibitors by fluoresence polarization assay | PABPC1 | 359244 | 1307 |
| antiBacterial | E. coli | Escherichia coli (strain K12) | targetBased | uHTS identification of MazEF TA System activators via a fluorescence-based single-stranded RNase assay | MAZF | 348923 | 1104 |
| RPN11 | targetBased | uHTS identification of inhibitors of Rpn11 in a Fluorescent Polarization assay | RPN11 | 359244 | 2134 | ||
| antiBacterial | S. aureus | NadD_inhibitors | targetBased | uHTS identification of inhibitors of NadD in a Colorimetric assay | NaMNAT | 362063 | 2815 |
| muculoEskeletalConnective | bone disease | MMP14 | targetBased | uHTS identification of inhibitors of MT1-MMP activation in a fluoresence assay | MMP14 | 361500 | 222 |
| cancer | neoplastic disease or syndrome | UBE2M | targetBased | uHTS identification of inhibitors of cullin neddylation in a TR-FRET assay | UBE2M | 363840 | 2123 |
| cancer | cancerGeneral | HIF-2a_inhibitors | targetBased | uHTS identification of HIF-2a Inhibitors in a luminesence assay | EPAS1 | 363840 | 2624 |
| muculoEskeletalConnective | non-syndromic polydactyly | GLI1 | targetBased | uHTS identification of Gli-Sufu Antagonists in a luminescence reporter assay | GLI1 | 338328 | 2501 |
| cancer | cancerGeneral | DNMT1 | targetBased | uHTS identification of DNMT1 inhibitors in a Fluorescent Molecular Beacon assay | DNMT1 | 359244 | 2975 |
| antiBacterial | Clostridium kluyveri | DiaphoraseInhibitors | targetBased | uHTS Identification of Diaphorase Inhibitors and Chemcical Oxidizers: Counter Screen for Diaphorase-based Primary Assays | DLD | 194152 | 1342 |
| rareDiseases | cysticFibrosis | NFKB1 | pathwayBased | uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | 359244 | 3094 |
| cancer | metastasis | CXCR6_inhibitors | targetBased | uHTS identification of CXCR6 Inhibitors in a B-arrestin luminescence assay | CXCR6 | 362063 | 1298 |
| cancer | neoplastic disease or syndrome | RUNX1 | targetBased | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay. | RUNX1 | 218234 | 1620 |
| cancer | neoplastic disease or syndrome | RUNX1 | targetBased | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb via a fluorescence resonance energy transfer (FRET) assay. | RUNX1 | 215667 | 993 |
| cancer | neoplastic disease or syndrome | TNFRSF10B | targetBased | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay | TNFRSF10B | 363840 | 3764 |
| antiViral | HIV | APOBEC3G_inhibitors | targetBased | uHTS identification of APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | APOBEC3G | 331753 | 931 |
| antiViral | HIV | APOBEC3A_inhibitors | targetBased | uHTS identification of APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | APOBEC3A | 331753 | 1372 |
| nervousSystem | drugAddiction | CRHBP_antagonists | targetBased | uHTS identification of antagonists of the CRF-binding protein and CRF-R2 receptor complex | CRHBP | 348923 | 2056 |
| biologicalProcess | toolCompounds | CRHBP_agonists | targetBased | uHTS identification of agonists of the CRF-binding protein and CRF-R2 receptor complex | CRHBP | 348923 | 1622 |
| respiratory | respiratory system disease | UBE2I | targetBased | uHTS HTRF assay for identification of inhibitors of SUMOylation | UBE2I | 290915 | 1039 |
| TNFSF10 | targetBased | uHTS for the identification of compounds that potentiate TRAIL-induced apoptosis of cancer cells | TNFSF10 | 217035 | 883 | ||
| biologicalProcess | autophagy | EIF4E_inhibition | targetBased | uHTS for Small Molecule Inhibitors of Eukaryotic Translation Initiation | EIF4E | 217332 | 799 |
| antiViral | EBV | Epstein-Barr virus | targetBased | uHTS for Small Molecule Inhibitiors of Epstein-Barr Virus Inhibitors | Q1HVG2 | 218602 | 926 |
| cancer | neoplastic disease or syndrome | MDM4 | targetBased | uHTS for identification of Inhibitors of Mdm2/MdmX interaction in luminescent format. | MDM4 | 331671 | 10022 |
| nervousSystem | neurodegeneration | calpainInhibitors | targetBased | uHTS for Calpain Inhibitors | CAPN2 | 218602 | 799 |
| YWHAZ | targetBased | uHTS for 14-3-3/Bad interaction inhibitors | YWHAZ | 217332 | 1549 | ||
| cancer | neoplastic disease or syndrome | SENP8 | targetBased | uHTS Fluorescent Assay Using Nedd8 Protein Substrate for Identification of Inhibitors of Sentrin-Specific Protease 8 (SENP8) | SENP8 | 363840 | 2341 |
| HKDC1 | targetBased | uHTS Fluorescent assay for identification of inhibitors of hexokinase domain containing I (HKDC1) | HKDC1 | 340696 | 540 | ||
| biologicalProcess | autophagy | ATG4B_inhibitors | pathwayBased | uHTS fluorescent assay for identification of inhibitors of ATG4B | ATG4B | 340119 | 1734 |
| nervousSystem | neurodegeneration | APAF1_inhibitors | targetBased | uHTS Fluorescent assay for identification of inhibitors of Apaf-1 | APAF1 | 331671 | 2353 |
| cancer | cancerGeneral | APAF1_activators | targetBased | uHTS Fluorescent assay for identification of activators of Apaf-1 | APAF1 | 331671 | 1041 |
| cancer | neoplastic disease or syndrome | PABPC1 | targetBased | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (PABP) | PABPC1 | 290915 | 2982 |
| cancer | cancerGeneral | EIF4H | targetBased | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) | EIF4H | 290915 | 2744 |
| antiViral | HIV | HIV type 1 | targetBased | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. | ENV | 292323 | 890 |
| biologicalProcess | nervousSystemDevelopment | CTDSP1_inhibitors | targetBased | uHTS Colorimetric assay for identification of inhibitors of Scp-1 | CTDSP1 | 340696 | 2986 |
| cancer | cancerGeneral | VHR1_inhibitors | targetBased | uHTS absorbance assay for the identification of compounds that inhibit VHR1. | DUSP3 | 291006 | 1524 |
| reproductiveSystem | sex hormone-binding globulin measurement | PHOSPHO1 | targetBased | uHTS absorbance assay for the identification of compounds that inhibit PHOSPHO1 | PHOSPHO1 | 288321 | 3164 |
| prionDisease | prionDisease | PRNP | targetBased | TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | 369953 | 1596 |
| metabolicEndocrine | obesity | MC4R | targetBased | TRFRET-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): antagonists of MC4R | MC4R | 356160 | 1703 |
| antiViral | HIV | HIV type 1 | targetBased | TRFRET-based biochemical primary high throughput screening assay to identify small molecules that bind to the HIV-1-gp120 binding antibody, PG9 | ENV | 362577 | 1546 |
| cancer | leukemia | ABL1_interaction | targetBased | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | ABL1 | 359207 | 1432 |
| antiViral | HIV | PSIP1 | targetBased | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of HIV-1 LEDGF/p75 DNA Integration | PSIP1 | 369953 | 2353 |
| cancer | Reactivate the silenced genes in cancer cells | MBD2 | targetBased | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide | MBD2 | 369953 | 1149 |
| antiViral | HCV | Hepacivirus hominis | targetBased | TR-FRET-based primary biochemical high-throughput screening assay to identify inhibitors of Hepatitis C Virus (HCV) core protein dimerization | ABC47431 | 302663 | 998 |
| nervousSystem | neurodegeneration | NR2E3 | targetBased | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). | NR2E3 | 314998 | 380 |
| immune | Immune dysregulation disease with immunodeficiency | IFNG | targetBased | Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | 67275 | 2509 |
| metabolicEndocrine | thyroid disease | THRB | targetBased | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | 276265 | 806 |
| cardioVascular | antithrombotic | F2_modulation | targetBased | Thrombin 1536 HTS | F2 | 217233 | 557 |
| antiBacterial | K. pneumonia | Klebsiella pneumonia SSB-PriA interaction | targetBased | SSB-PriA antibiotic resistant target AlphaScreen | SSB | 431236 | 2568 |
| respiratory | pulmonary function measurement | ID4 | targetBased | SMM ID4 Measured in Biochemical System Using Small Molecule MicroArray - 2128-01_Other_SinglePoint_HTS_Activity | ID4 | 31324 | 362 |
| respiratory | bronchial disease | IL1RL1 | targetBased | Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | 75924 | 1804 |
| antiMicrobial | giardiasis | Giardia lamblia | phenotypic | Small Molecules that selectively kill Giardia lamblia: qHTS | 342452 | 530 | |
| cancer | hepatocellularCarcinoma | miR122_activators | phenotypic | Small molecule inhibitors of miR122 Measured in Cell-Based System Using Plate Reader - 2144-01_Inhibitor_SinglePoint_HTS_Activity | 333274 | 1022 | |
| antiViral | HCV | miR122_inhibitors | phenotypic | Small molecule inhibitors of miR122 Measured in Cell-Based System Using Plate Reader - 2144-01_Activator_SinglePoint_HTS_Activity | 333274 | 472 | |
| cancer | neoplastic disease or syndrome | FGF22_inhibitors | targetBased | Small Molecule Inhibitors of FGF22-Mediated Excitatory Synaptogenesis & Epilepsy Measured in Biochemical System Using RT-PCR - 7012-01_Inhibitor_SinglePoint_HTS_Activity | FGF22 | 339650 | 5128 |
| antiBacterial | antibacterials | TB | phenotypic | several TB strains | |||
| biologicalProcess | secretionPath | Modulators of Post-Golgi Transport | phenotypic | Screening for Modulators of Post-Golgi Transport, Control Strain | 97518 | 4851 | |
| antiBacterial | S. Pneumoniae | Streptococcus pneumoniae serotype 2 (strain D39 / NCTC 7466) | targetBased | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - PMK | MVAK2 | 65392 | 319 |
| antiBacterial | S. Pneumoniae | Streptococcus Pneumoniae | targetBased | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - MK | MK | 65241 | 316 |
| antiBacterial | S. Pneumoniae | Streptococcus pneumoniae serotype 2 (strain D39 / NCTC 7466) | targetBased | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC | MVAD | 65385 | 320 |
| antiBacterial | tuberculosis | Mycobacterium Tuberculosis sensitization to betaLactam | phenotypic | Screen to Identify Novel Compounds That Sensitize Mycobacterium Tuberculosis to Beta-lactam Antibiotics | 327901 | 876 | |
| cancer | neoplastic disease or syndrome | SMARCA4 | targetBased | Screen for inhibitors of the SWI/SNF chromatin remodeling complex (esBAF) in mouse embryonic stem cells with Luciferase reporter assay Measured in Cell-Based System Using Plate Reader - 2141-01_Inhibitor_SinglePoint_HTS_Activity | SMARCA4 | 344733 | 7043 |
| cancer | cancerGeneral | RMI FANCM intereaction | phenotypic | Screen for inhibitors of RMI FANCM (MM2) intereaction | 69794 | 402 | |
| biologicalProcess | toolCompounds | lifespan | phenotypic | Screen for Chemicals that Shorten Yeast Lifespan | 138737 | 710 | |
| cancer | cancerGeneral | RAM network inhibitors | phenotypic | Screen for Chemicals that Inhibit the RAM Network | 194550 | 3545 | |
| biologicalProcess | senescence | lifespan | phenotypic | Screen for Chemicals that Extend Yeast Lifespan | 132777 | 904 | |
| muculoEskeletalConnective | osteoporosis | Schnurri-3 Inhibitors | targetBased | Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Based System Using Plate Reader - 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | HIVEP3 | 356883 | 1841 |
| nervousSystem | neurodegeneration | S100A4 | targetBased | S100A4: HTS Measured in Biochemical System Using Plate Reader - 7045-01_Inhibitor_SinglePoint_HTS_Activity | S100A4 | 352235 | 501 |
| antiFungal | candidiasis | Candida albicans (strain SC5314 / ATCC MYA-2876) (Yeast) | targetBased | Rtt109/Vps75 Measured in Biochemical System Using Plate Reader - 2106-01_Inhibitor_SinglePoint_HTS_Activity | RTT109 | 328088 | 521 |
| cancer | neoplastic disease or syndrome | RBX1 | targetBased | ROC1-CUL1 CTD Inhibitor di-Ub FRET Primary HTS Screen | RBX1 | 143816 | 859 |
| muculoEskeletalConnective | bone disease | GRK2 | targetBased | RNA aptamer-based HTS for inhibitors of GRK2 | GRK2 | 327939 | 1924 |
| antiBacterial | tuberculosis | RmlC_inhibitors | phenotypic | Rml C and D inhibition 384-well mixture HTS | 106271 | 417 | |
| biologicalProcess | EpigeneticControl | EpigeneticControl | phenotypic | Quantitative High-Throughput Screen for Regulators of Epigenetic Control | 272097 | 537 | |
| industrial | lipidBiosynthesis | fuelBiosynthesis | phenotypic | qHTS screening for TAG (triacylglycerol) accumulators in algae | 43680 | 367 | |
| cancer | cancerGeneral | ATAD5_inhibitors | targetBased | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 | ATAD5 | 330107 | 7652 |
| cancer | cancerGeneral | ATAD5_inhibitors | targetBased | qHTS screen for small molecules that induce genotoxicity in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 | ATAD5 | 330109 | 4174 |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | TP53 | 124022 | 1156 |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | TP53 | 125394 | 1890 |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Permissive Temperature | TP53 | 54513 | 338 |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Nonpermissive Temperature | TP53 | 54509 | 528 |
| antiMicrobial | malaria | Plasmodium falciparum | phenotypic | qHTS Primary assay for Inhibitors of Plasmodium falciparum Dd2 growth in vitro | 123608 | 5316 | |
| antiViral | SARS-CoV | SARS-CoV | targetBased | qHTS of Yeast-based Assay for SARS-CoV PLP | REP | 328641 | 609 |
| antiMicrobial | trypanosomiasis | T. brucei | phenotypic | qHTS of Trypanosoma Brucei Inhibitors | TB08.30K1.730 | 406726 | 491 |
| nervousSystem | inherited neurodegenerative disorder | TARDBP | pathwayBased | qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen | TARDBP | 45163 | 203 |
| nervousSystem | neurodegeneration | TARDBP | pathwayBased | qHTS of TDP-43 Inhibitors | TARDBP | 403703 | 7150 |
| immune | COPD | Nrf2 activators | pathwayBased | qHTS of Nrf2 Activators | NFE2L2 | 403871 | 1243 |
| cancer | neoplasm of thorax | IL2 | targetBased | qHTS of IL-2 Activators | IL2 | 364617 | 238 |
| metabolicEndocrine | T2Diabetes | GLP1R PAMs | targetBased | qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R | 405130 | 6428 |
| metabolicEndocrine | endocrine pancreas disorder | GLP1R | targetBased | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | 405130 | 6428 |
| metabolicEndocrine | T2Diabetes | GLP1R agonists | targetBased | qHTS of GLP-1 Receptor Agonists | GLP1R | 373462 | 23 |
| nervousSystem | neurodegeneration | D3_PAMs | targetBased | qHTS of D3 Dopamine Receptor Potentiators: qHTS | DRD3 | 407539 | 2380 |
| nervousSystem | drugAddiction | D3_antagonists | targetBased | qHTS of D3 Dopamine Receptor Antagonist: qHTS | DRD3 | 364051 | 9106 |
| nervousSystem | neurodegeneration | D3_agonists | targetBased | qHTS of D3 Dopamine Receptor Agonist: qHTS | DRD3 | 407539 | 2380 |
| nervousSystem | inherited neurodegenerative disorder | SNCA | pathwayBased | qHTS of alpha-syn Inhibitors | SNCA | 368791 | 501 |
| nervousSystem | Huntington disease | HTT | targetBased | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Cytoprotection (ATP) | HTT | 223611 | 305 |
| nervousSystem | Huntington disease | HTT | targetBased | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Aggregate Formation (GFP) | HTT | 220571 | 2380 |
| antiBacterial | E. coli | Escherichia coli (strain K12) | targetBased | qHTS Inhibitors of AmpC Beta-Lactamase (assay without detergent) | AMPC | 330677 | 1730 |
| nervousSystem | sporadic amyotrophic lateral sclerosis | FUS_asupressors | targetBased | qHTS for Suppressors of FUS Proteinopathy: Primary screen using FUS-linked yeast assay | FUS | 385746 | 932 |
| antiViral | VACV | Vaccinia virus (VACV) | phenotypic | qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: Venus Reporter Primary qHTS | 3707576 | 326363 | 1520 |
| antiViral | VACV | Vaccinia virus (VACV) | phenotypic | qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: mCherry Reporter Primary qHTS | 3707576 | 306737 | 1931 |
| psychiatricDisorder | anxiety | TRHR | targetBased | qHTS for Small Molecule Agonists and Allosteric Enhancers of Human TRH Receptor: Primary Screen for Enhancers | TRHR | 361330 | 2424 |
| metabolicEndocrine | thyroid disease | TRHR | targetBased | qHTS for Small Molecule Agonists and Allosteric Enhancers of Human TRH Receptor: Primary Screen for Agonists. | TRHR | 361330 | 651 |
| nervousSystem | neurodegeneration | PI4K2A | targetBased | qHTS for small molecular inhibitors of PI4K2A | PI4K2A | 414643 | 532 |
| muculoEskeletalConnective | bone development disease | PTH1R | targetBased | qHTS for PTHR1 Agonists: Primary Screen | PTH1R | 405685 | 308 |
| cancer | neoplastic disease or syndrome | WRN | targetBased | qHTS for Inhibitors of WRN Helicase | WRN | 364011 | 1678 |
| antiViral | HIV | APOBEC3G_inhibitors | targetBased | qHTS for Inhibitors of Vif-A3G Interactions: qHTS | APOBEC3G | 402348 | 311 |
| antiViral | HIV | APOBEC3F_inhibitors | targetBased | qHTS for Inhibitors of Vif-A3F Interactions: qHTS | APOBEC3F | 383848 | 765 |
| immune | fibrosis | TGFB1 | pathwayBased | qHTS for Inhibitors of TGF-b | TGFB1 | 403345 | 4970 |
| nervousSystem | neurodegeneration | MAPT | pathwayBased | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | 267412 | 5703 |
| nervousSystem | inherited neurodegenerative disorder | MAPT | pathwayBased | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | 271402 | 1048 |
| immune | autoimmuneDisorders | RORCgammaPathwayInhibitors | pathwayBased | qHTS for inhibitors of ROR gamma transcriptional activity | RORC | 305439 | 16717 |
| cancer | neoplastic disease or syndrome | POLK | targetBased | qHTS for Inhibitors of Polymerase Kappa | POLK | 395295 | 2034 |
| respiratory | lower respiratory tract disease | POLI | targetBased | qHTS for Inhibitors of Polymerase Iota | POLI | 386063 | 3989 |
| geneticDisorder | Rare genetic skin disease | POLH | targetBased | qHTS for Inhibitors of Polymerase Eta | POLH | 388717 | 4730 |
| immune | type II hypersensitivity reaction disease | PLK1 | targetBased | qHTS for Inhibitors of PLK1-PDB (polo-like kinase 1 - polo-box domain): Primary Screen | PLK1 | 364065 | 10181 |
| nervousSystem | neurodegeneration | PIP4K2A | targetBased | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) | PIP4K2A | 328860 | 4078 |
| HEL-S-26 | targetBased | qHTS for Inhibitors of mutant isocitrate dehydrogenase 1 (IDH1): qHTS | HEL-S-26 | 387604 | 365 | ||
| cardioVascular | Rare genetic cardiac disease | KCNH2 | targetBased | qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | 343666 | 1267 |
| psychiatricDisorder | schizophrenia | KCNH2 | targetBased | qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | 342084 | 3260 |
| immune | Inflammation CASP COPD | IL-1b Inflammasome | pathwayBased | qHTS for Inhibitors of Inflammasome Signaling: IL-1-beta AlphaLISA Primary Screen | IL1B | 362051 | 17187 |
| nervousSystem | inherited neurodegenerative disorder | TDP1 | targetBased | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | TDP1 | 416856 | 49238 |
| nervousSystem | inherited neurodegenerative disorder | TDP1 | targetBased | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | TDP1 | 416824 | 63248 |
| geneticDisorder | autosomal recessive disease | GLS | targetBased | qHTS for Inhibitors of Glutaminase (GLS) | GLS | 405291 | 844 |
| hematologic | inherited bleeding disorder, platelet-type | PLAU | targetBased | qHTS for Inhibitors of Cell Surface uPA Generation | PLAU | 325247 | 1021 |
| antiViral | Margburg virus | Margburg virus entry | phenotypic | qHTS for inhibitors of binding or entry into cells for Marburg Virus | 284160 | 4700 | |
| antiViral | LassaVirus | Lassa virus entry | phenotypic | qHTS for Inhibitors of binding or entry into cells for Lassa Virus | 297156 | 3648 | |
| antiMicrobial | malaria | Plasmodium falciparum | targetBased | qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Primary Screen | AMA1-RON | 364096 | 735 |
| cancer | glioma | gliomaWithIdh1Mutations | targetBased | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line | HEL-S-26 | 364464 | 5966 |
| cancer | glioma | gliomaWithIdh1Mutations | phenotypic | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line | 364464 | 7438 | |
| nervousSystem | neurodegeneration | APP_inhibitors | targetBased | qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP | 404343 | 257 |
| rareDiseases | McCune-Albright syndrome (MAS) | GNAS | targetBased | qHTS for Antagonists of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS | GNAS | 337446 | 1356 |
| metabolicEndocrine | thyroid disease | RAPGEF3 | targetBased | qHTS for Antagonist of cAMP-regulated guanine nucleotide exchange factor 3 (EPAC1): primary screen | RAPGEF3 | 364614 | 517 |
| psychiatricDisorder | mental process | RAPGEF4 | targetBased | qHTS for Antagonist of cAMP-regulated guanine nucleotide exchange factor 2 (EPAC2): primary screen | RAPGEF4 | 364614 | 663 |
| geneticDisorder | developmental defect during embryogenesis | MCOLN1 | targetBased | qHTS for Agonists of the Human Mucolipin Transient Receptor Potential 1 (TRPML1) | MCOLN1 | 400814 | 482 |
| cancer | neoplastic disease or syndrome | GPR32 | targetBased | qHTS for Agonists of Human Resolvin D1 Receptor DRV1 | GPR32 | 47473 | 1217 |
| metabolicEndocrine | hereditary hypoparathyroidism | GNAS | targetBased | qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS | GNAS | 334825 | 423 |
| psychiatricDisorder | mental process | RAPGEF4 | targetBased | qHTS for Agonist of cAMP-regulated guanine nucleotide exchange factor 4 (EPAC2): primary screen | RAPGEF4 | 364614 | 290 |
| metabolicEndocrine | thyroid disease | RAPGEF3 | targetBased | qHTS for Agonist of cAMP-regulated guanine nucleotide exchange factor 3 (EPAC1): primary screen | RAPGEF3 | 364614 | 268 |
| rareDiseases | muscularDistrophy | CGA_integrin_activators | targetBased | qHTS for Activators of Integrin-Mediated Alleviation for Muscular Dystrophy | CGA | 345855 | 222 |
| immune | autoimmuneDisorders | RORCgammaPathwayInhibitors | pathwayBased | qHTS assay to identify small molecule antagonists of the retinoid-related orphan receptor gamma (ROR-gamma) signaling pathway | RORC | 7671 | 874 |
| metabolicEndocrine | insulinSensitization | RXRA_pathway_agonists | pathwayBased | qHTS assay to identify small molecule agonists of the RXR signaling pathway: | RXR | 7671 | 173 |
| cancer | breastCancer | BRCA1 activation | pathwayBased | qHTS Assay to Identify Small Molecule Activators of BRCA1 Expression | BRCA1 | 376029 | 3978 |
| antiMicrobial | trypanosomiasis | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | targetBased | qHTS Assay to Find Inhibitors of T. brucei phosphofructokinase | TB03.3K10.320 | 330677 | 557 |
| antiMicrobial | schistosomiasis | Schistosoma mansoni (Blood fluke) | targetBased | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | TGR | 356643 | 10735 |
| cancer | neoplastic disease or syndrome | L3MBTL1 | targetBased | qHTS Assay for the Inhibitors of L3MBTL1 | L3MBTL1 | 225309 | 1492 |
| nervousSystem | neurodegeneration | FEN1_inhibitors | targetBased | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). | FEN1 | 386270 | 1331 |
| nervousSystem | inherited neurodegenerative disorder | MAPT | targetBased | qHTS Assay for Tau Filament Binding | MAPT | 69668 | 1391 |
| biologicalProcess | mitochondrialFusion | mitochondrialFusion | phenotypic | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion | 322166 | 738 | |
| immune | COPD | Antioxidant Response Element | phenotypic | qHTS assay for small molecule agonists of the antioxidant response element (ARE) signaling pathway | 7671 | 943 | |
| cancer | cancerGeneral | TP53 | pathwayBased | qHTS assay for re-activators of p53 using a Luc reporter | TP53 | 321427 | 201 |
| rareDiseases | Niemann Pick Type C (NPC) | RAB9A | pathwayBased | qHTS Assay for Rab9 Promoter Activators | RAB9A | 320603 | 9133 |
| antiMicrobial | trypanosomiasis | Trypanosoma cruzi | targetBased | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent) | P25779 | 195013 | 4500 |
| antiMicrobial | trypanosomiasis | Trypanosoma cruzi | targetBased | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent) | P25779 | 195013 | 848 |
| rareDiseases | Niemann Pick Type C (NPC) | NPC1 | pathwayBased | qHTS Assay for NPC1 Promoter Activators | NPC1 | 320682 | 7575 |
| cancer | cancerGeneral | miRNA_modulators | phenotypic | qHTS Assay for Modulators of miRNAs and/or Inhibitors of miR-21 | 333510 | 3282 | |
| cancer | cancerGeneral | MDR1-selective compounds | targetBased | qHTS assay for MDR1-selective chemotherapeutics: Primary screen using the parental adenocarcinoma cell KB-3-1 | ABCB1 | 395981 | 5516 |
| cancer | cancerGeneral | MDR1-selective compounds | targetBased | qHTS assay for MDR1-selective chemotherapeutics: Primary screen using the drug-selected MDR subline cells KB-V1 | ABCB1 | 396029 | 13426 |
| metabolicEndocrine | obesity | lipidStorageInhibitors | phenotypic | qHTS Assay for Lipid Storage Modulators in Drosophila S3 Cells | 320858 | 2061 | |
| cancer | leukemia | Menin-MLL_inhibitors | targetBased | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide | MEN1 | 263421 | 615 |
| nervousSystem | inherited neurodegenerative disorder | TDP1 | targetBased | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | TDP1 | 344442 | 978 |
| nervousSystem | inherited auditory system disease | SIX1 | targetBased | qHTS Assay for Inhibitors of the Six1/Eya2 Interaction | SIX1 | 364053 | 2026 |
| antiViral | HCMV | HCMV inhibitors | phenotypic | qHTS Assay for inhibitors of the human cytomegalovirus (HCMV) | 403256 | 18370 | |
| cancer | cancerGeneral | APEX1_inhibitors | targetBased | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | APEX1 | 345898 | 1172 |
| antiViral | HIV | HIV-VPR | targetBased | qHTS Assay for Inhibitors of the HIV-1 protein Vpr | VPR | 361879 | 750 |
| cancer | neoplastic disease or syndrome | MAPK1 | pathwayBased | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | 131324 | 544 |
| cancer | neoplastic disease or syndrome | MAPK1 | pathwayBased | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | 70898 | 707 |
| geneticDisorder | developmental defect during embryogenesis | RBBP8 | targetBased | qHTS Assay for Inhibitors of the CtBP/E1A Interaction | RBBP8 | 335214 | 1652 |
| nervousSystem | Neurodevelopmental disorder | GNAI1 | targetBased | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) | GNAI1 | 229888 | 1007 |
| cancer | neoplastic disease or syndrome | RECQL | targetBased | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | RECQL | 234915 | 1245 |
| SNUPN | targetBased | qHTS Assay for Inhibitors of RanGTP induced Rango (Ran-regulated importin-beta cargo) - Importin beta complex dissociation | SNUPN | 340719 | 242 | ||
| cancer | neoplastic disease or syndrome | TXNRD1 | targetBased | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | TXNRD1 | 386663 | 3977 |
| antiMicrobial | leishmaniasis | Leishmania mexicana | targetBased | qHTS Assay for Inhibitors of Leishmania Mexicana Pyruvate Kinase (LmPK) | PYK | 292732 | 1088 |
| biologicalProcess | epigenetics | KDM4A | targetBased | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain | KDM4A | 384527 | 16920 |
| antiViral | H1N1 | Influenza NS1 | targetBased | qHTS Assay for Inhibitors of Influenza NS1 Protein Function | NS1 | 269561 | 1073 |
| cancer | cancerGeneral | lactateDehydrogenaseInhibitors | targetBased | qHTS assay for inhibitors of human lactate dehydrogenase | LDHA | 476056 | 732 |
| geneticDisorder | developmental defect during embryogenesis | HSD17B10 | targetBased | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | HSD17B10 | 73912 | 5649 |
| muculoEskeletalConnective | hypertrophic osteoarthropathy, primary, autosomal recessive, 1 | HPGD | targetBased | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | HPGD | 148480 | 6428 |
| cancer | cancerGeneral | EHMT2_inhibitors | targetBased | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | EHMT2 | 348338 | 30875 |
| antiViral | HCV | HCV inhibitors | phenotypic | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) | 339573 | 11624 | |
| geneticDisorder | developmental defect during embryogenesis | HSD17B10 | targetBased | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) | HSD17B10 | 72072 | 2464 |
| cancer | neoplastic disease or syndrome | KAT2A | targetBased | qHTS Assay for Inhibitors of GCN5L2 | KAT2A | 381571 | 792 |
| antiMicrobial | giardiasis | Giardia intestinalis (strain ATCC 50803 / WB clone C6) (Giardia lamblia) | targetBased | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia | FBA | 287738 | 2034 |
| nervousSystem | neurodegeneration | POLB | targetBased | qHTS Assay for Inhibitors of DNA Polymerase Beta | POLB | 334457 | 4509 |
| cancer | cancerGeneral | BLM_inhibitors | targetBased | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | BLM | 347933 | 673 |
| nervousSystem | neurodevelopmentalDisorders | BAZ2B_modulators | targetBased | qHTS Assay for Inhibitors of BAZ2B | BAZ2B | 356826 | 15709 |
| antiBacterial | B. subtilis | Bacillus subtilis | targetBased | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | FFP | 306599 | 10840 |
| metabolicEndocrine | obesity | ALDH1A1_inhibitors | targetBased | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | ALDH1A1 | 216881 | 16026 |
| cancer | cancerGeneral | ALOX15B_inhibitors | targetBased | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) | ALOX15B | 107252 | 595 |
| immune | immunomodulation | ALOX15_inhibitors | targetBased | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | ALOX15 | 73174 | 1034 |
| cancer | neoplastic disease or syndrome | KDM4E | targetBased | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) | KDM4E | 226914 | 3523 |
| GBA | targetBased | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | GBA | 321552 | 295 | ||
| muculoEskeletalConnective | familial cardiomyopathy | GAA_inhibitors | targetBased | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | GAA | 302297 | 1165 |
| psychiatricDisorder | mental or behavioural disorder | IMPA1 | targetBased | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | IMPA1 | 205582 | 727 |
| nervousSystem | ataxiaTelangiectasia | ATM_modulators | targetBased | qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM | 322361 | 619 |
| visualSystem | eye disease | FTL | targetBased | qHTS Assay for Identification of Novel General Anesthetics | FTL | 341499 | 255 |
| antiViral | FMDV | Foot-and-mouth disease virus | phenotypic | qHTS Assay for Foot and Mouth Disease Virus Antivirals: Primary Screen against the MLPCN compound library | AAA42670 | 404063 | 1959 |
| rareDiseases | SMA | SMN1; SMN2 | pathwayBased | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | SMN1; SMN2 | 208489 | 5817 |
| cancer | cancerGeneral | Disrupters of an Hsp90 Co-Chaperone Interaction | phenotypic | qHTS Assay for Disrupters of an Hsp90 Co-Chaperone Interaction | 69668 | 300 | |
| antiBacterial | anthrax | Bacillus anthracis Lethal Toxin Internalization | phenotypic | qHTS Assay for Anthrax Lethal Toxin Internalization | 68961 | 466 | |
| immune | fibrosis | relaxin PMs | targetBased | qHTS Assay for Antagonists of the Relaxin Receptor RXFP1Taking the negative queue for PMs | RXFP1 | 350177 | 2058 |
| cancer | cancerGeneral | relaxinInhibitors | targetBased | qHTS Assay for Antagonists of the Relaxin Receptor RXFP1 | RXFP1 | 350177 | 2058 |
| psychiatricDisorder | anxiety | NPSR1 | targetBased | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | NPSR1 | 220862 | 2309 |
| biologicalProcess | apoptosisInhibition | caspase1Inhibitors | phenotypic | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1: Spectroscopic Profiling in AFC Spectral Region | 73912 | 779 | |
| metabolicEndocrine | thyroid disease | TSHR | targetBased | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | TSHR | 72026 | 1794 |
| metabolicEndocrine | thyroid disease | TSHR | targetBased | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor | TSHR | 72026 | 352 |
| immune | fibrosis | RXFP1 | targetBased | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 | RXFP1 | 362198 | 1084 |
| nervousSystem | neurodegeneration | PKM | targetBased | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase | PKM | 263662 | 892 |
| muculoEskeletalConnective | familial cardiomyopathy | GAA | targetBased | qHTS Assay for Activators of Human alpha-Glucosidase as a Potential Chaperone Treatment of Pompe Disease | GAA | 199169 | 715 |
| antiBacterial | B. subtilis | Bacillus subtilis (strain 168) | targetBased | qHTS Assay for Activators of ClpP | CLPP | 338378 | 6439 |
| antiViral | SARS-CoV | SARS-CoV | targetBased | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) | AAZ82016 | 290726 | 405 |
| antiMicrobial | malaria | Plasmodium falciparum (isolate 3D7) | targetBased | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | M18AAP | 290726 | 3497 |
| antiMicrobial | malaria | PFM18AAPinhibitorsCounterscreen | targetBased | QFRET-based counterscreen for PFM18AAP inhibitors: biochemical high throughput screening assay to identify inhibitors of the Cathepsin L proteinase (CTSL1). | CTSL1 | 302663 | 1482 |
| cancer | breastCancer | ADAM17_inhibitors | targetBased | QFRET-based biochemical primary high throughput screening assay to identify exosite inhibitors of ADAM17. | ADAM17 | 369953 | 3080 |
| cancer | breastCancer | ADAM10_inhibitors | targetBased | QFRET-based biochemical primary high throughput screening assay to identify exosite inhibitors of ADAM10. | ADAM10 | 369953 | 2294 |
| cancer | neoplastic disease or syndrome | PLA2G3 | targetBased | QFRET-based biochemical high throughput primary assay to identify inhibitors of human group III secreted phospholipase A2 enzyme (HGIII-sPLA2) | PLA2G3 | 369953 | 2089 |
| antiBacterial | Geobacillus stearothermophilus | Geobacillus stearothermophilus (Bacillus stearothermophilus) | targetBased | Pyruvate Kinase | PYK | 51415 | 602 |
| antiBacterial | E. coli | Escherichia coli (strain K12) | targetBased | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) | AMPC | 69668 | 1256 |
| immune | rheumatoidArthritis | Inhibitors of CD40 Signaling | phenotypic | Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based System Using Plate Reader - 7124-01_Inhibitor_SinglePoint_HTS_Activity | 82418 | 778 | |
| psychiatricDisorder | mental or behavioural disorder | KDM5B | targetBased | Primary screen for KDM5B Histone Demethylases FDH-coupled qHTS | KDM5B | 217819 | 5697 |
| metabolicEndocrine | endocrine pancreas disorder | INS | targetBased | Primary screen for compounds that inhibit Insulin promoter activity in TRM-6 cells | INS | 127961 | 1153 |
| nervousSystem | AD | APP_inhibitors | pathwayBased | Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP | 193714 | 1590 |
| metabolicEndocrine | endocrine pancreas disorder | INS | targetBased | Primary screen for compounds that activate Insulin promoter activity in TRM-6 cells | INS | 128695 | 1039 |
| nervousSystem | neurodegeneration | APP_inhibitors | pathwayBased | Primary screen for compounds that activate Alzheimer's amyloid precursor | APP | 193400 | 1987 |
| NTMT1 | targetBased | Primary qHTS for Inhibitors of N-terminal methyltransferase 1 (NTMT1): MTaseGlo Assay | NTMT1 | 56440 | 1336 | ||
| nervousSystem | spinocerebellarAtaxia | ATXN2_repressors | targetBased | Primary qHTS for Inhibitors of ATXN expression | ATXN2 | 358434 | 2554 |
| nervousSystem | Huntington disease | HTT | targetBased | Primary qHTS for Identification of Small Molecule Inhibitors of Huntingtin Promoter Activity | HTT | 48068 | 449 |
| antiMicrobial | malaria | Plasmodium falciparum | phenotypic | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | 323200 | 22332 | |
| antiMicrobial | malaria | Plasmodium falciparum | phenotypic | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | 304969 | 18055 | |
| nervousSystem | neurodegeneration | IP6K1 | targetBased | Primary qHTS assay for small molecule inhibitors of Inositol hexaphosphate kinase 1 (IP6K1) | IP6K1 | 143229 | 1157 |
| cancer | cancerGeneral | ALOX12_inhibitors | targetBased | Primary qHTS assay for inhibitors of human arachidonate 12S-lipoxygenase (ALOX12): Round 2 | ALOX12 | 564288 | 6030 |
| nervousSystem | inherited neurodegenerative disorder | GPT2 | targetBased | Primary qHTS assay for inhibitors of Glutamate pyruvate transaminase 2 (GPT2) | GPT2 | 98912 | 236 |
| nervousSystem | inherited neurodegenerative disorder | SNCA | pathwayBased | Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression | SNCA | 140118 | 236 |
| immune | immunomodulation | AICDA_inhibitors | targetBased | Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA | 90878 | 289 |
| antiViral | FMDV | Foot-and-mouth disease virus | targetBased | Primary qHTS Assay for Foot and Mouth Disease Virus Antivirals against NCGC Sytravon and CBC Compound Libraries: Renilla Luciferase Signal | P03308 | 117258 | 373 |
| antiViral | FMDV | Foot-and-mouth disease virus | targetBased | Primary qHTS Assay for Foot and Mouth Disease Virus Antivirals against NCGC Sytravon and CBC Compound Libraries: Firefly Luciferase Signal | P03308 | 117258 | 273 |
| immune | type II hypersensitivity reaction disease | S1PR3 | targetBased | Primary HTS Assay for S1P3 Antagonists | S1PR3 | 169141 | 462 |
| immune | immunomodulation | NFkB nuclear translocation | phenotypic | Primary HTS assay for chemical potentiators of IL-1B stimulated NFkB nuclear translocation | 94231 | 282 | |
| immune | immunomodulation | VCAM1_expression | targetBased | Primary HTS assay for chemical inhibitors of TNF alpha stimulated VCAM1 expression | VCAM1 | 94498 | 457 |
| immune | immunomodulation | E-selectinExpression | targetBased | Primary HTS assay for chemical inhibitors of TNF alpha stimulated E-Selectin expression | SELE | 118096 | 843 |
| psychiatricDisorder | major depressive disorder | HTR1A | targetBased | Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) antagonists | HTR1A | 61606 | 416 |
| psychiatricDisorder | major depressive disorder | HTR1A | targetBased | Primary HTS assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) agonists | HTR1A | 64908 | 366 |
| immune | autoimmune disorder of the nervous system | S1PR1 | targetBased | Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | 55710 | 315 |
| TRPC4 | targetBased | Primary cell-based screen for identification of compounds that inhibit transient receptor potential cation channel C4 (TRPC4). | TRPC4 | 304001 | 1189 | ||
| biologicalProcess | toolCompounds | KCNK9_blockers | targetBased | Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9 | 305610 | 3794 |
| cardioVascular | arterial disorder | KCNK3 | targetBased | Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | 339674 | 2841 |
| nervousSystem | neurodegeneration | SLC5A7 | targetBased | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) | SLC5A7 | 306502 | 2634 |
| visualSystem | eye disease | SLC5A7 | targetBased | Primary cell-based screen for identification of compounds that allosterically activate the Choline Transporter (CHT) | SLC5A7 | 306502 | 1509 |
| TRPC4 | targetBased | Primary cell-based screen for identification of compounds that activate transient receptor potential cation channel C4 (TRPC4). | TRPC4 | 305600 | 1510 | ||
| nervousSystem | hearing disorder | S1PR2 | targetBased | Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | S1PR2 | 96879 | 207 |
| nervousSystem | hearing disorder | S1PR2 | targetBased | Primary Cell-Based High-Throughput Screening to Identify Agonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | S1PR2 | 96879 | 447 |
| immune | psoriasis | ANO1_inhibitors | targetBased | Primary cell-based high-throughput screening for identification of compounds that inhibit/block calcium-activated chloride channels (TMEM16A) | ANO1 | 306502 | 3633 |
| MGRG2 | targetBased | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | MGRG2 | 306502 | 3868 | ||
| MGRG2 | targetBased | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling | MGRG2 | 306502 | 1932 | ||
| respiratory | pulmonary arterial hypertension | ANO1_activators | targetBased | Primary cell-based high-throughput screening for identification of compounds that activate/potentiate calcium-activated chloride channels (TMEM16A) | ANO1 | 335180 | 1022 |
| MGRG2 | targetBased | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling | MGRG2 | 306502 | 1351 | ||
| biologicalProcess | proteinMisfolding | PERK_inhibitors | targetBased | Primary cell-based high-throughput screening assay to measure PERK inhibition | EIF2AK3 | 217959 | 370 |
| nervousSystem | neurodegeneration | Heat shock 70kDa protein 1A | pathwayBased | Primary cell-based high-throughput screening assay to identify transcriptional activators of heat shock protein 70 (Hsp70) | HSP70 | 196176 | 82 |
| cancer | neoplastic disease or syndrome | GALR2_antagonists | targetBased | Primary cell-based high-throughput screening assay to identify antagonists of Galanin Receptor 2 (GALR2) | GALR2 | 140088 | 548 |
| TRPN1 | targetBased | Primary cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel N1 (TRPN1) | TRPN1 | 217959 | 390 | ||
| nervousSystem | neurodegeneration | MCOLN3 | targetBased | Primary cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel ML3 (TRPML3) | MCOLN3 | 217959 | 632 |
| cancer | neoplastic disease or syndrome | GALR2 | targetBased | Primary cell-based high-throughput screening assay to identify agonists of Galanin Receptor 2 (GALR2) | GALR2 | 140088 | 678 |
| cancer | neoplastic disease or syndrome | NPY2R | targetBased | Primary cell-based high-throughput screening assay for potentiators or agonists of NPY-Y2 | NPY2R | 217959 | 969 |
| psychiatricDisorder | mental process | NPY1R | targetBased | Primary cell-based high-throughput screening assay for potentiators or agonists of NPY-Y1 | NPY1R | 217959 | 798 |
| immune | immunomodulation | inhibitors of TLR4-MyD88 binding | phenotypic | Primary cell-based high-throughput screening assay for inhibitors of TLR4-MyD88 binding | 195980 | 357 | |
| antiMicrobial | malaria | Inhibitors of Mosquito Biting Behavior | targetBased | Primary cell-based high-throughput screening assay for identification of small molecule agonists of Aedes aegypti NPYLR7 [Small Molecule Inhibitors of Mosquito Biting Behavior] | NPYLR7 | 265113 | 400 |
| cardioVascular | Rare genetic cardiac disease | KCNH2 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | 305610 | 1552 |
| psychiatricDisorder | cognitive disorder | RGS4 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate regulator of G-protein signaling 4 (RGS4) | RGS4 | 305610 | 2820 |
| cardioVascular | congenital heart disease | KCNQ1 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | 305610 | 1082 |
| nervousSystem | Rare genetic epilepsy | KCNQ2 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels | KCNQ2 | 305600 | 1644 |
| muculoEskeletalConnective | familial periodic paralysis | KCNJ2 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | 305610 | 2592 |
| psychiatricDisorder | cognitive disorder | RGS4 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that inhibit regulator of G-protein signaling 4 (RGS4) | RGS4 | 305610 | 1365 |
| nervousSystem | Rare genetic epilepsy | KCNQ2 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels | KCNQ2 | 305609 | 3405 |
| cardioVascular | congenital heart disease | KCNQ1 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | 305610 | 3878 |
| TRPC4 | targetBased | Primary cell-based high-throughput screening assay for identification of compounds that allosterically potentiate transient receptor potential cation channel C4 (TRPC4) | TRPC4 | 305600 | 1291 | ||
| psychiatricDisorder | anxiety | NPY1R | targetBased | Primary cell-based high-throughput screening assay for antagonists of NPY-Y1 | NPY1R | 196176 | 1984 |
| immune | immunomodulation | STAT3 | pathwayBased | Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | 194666 | 1722 |
| immune | immunomodulation | STAT3 | pathwayBased | Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | 194666 | 1772 |
| immune | Primary immunodeficiency due to a defect in innate immunity | STAT1 | targetBased | Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | 195980 | 695 |
| immune | immunomodulation | STAT1 activation | pathwayBased | Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 | 195980 | 5134 |
| cancer | neoplastic disease or syndrome | KLF5 | targetBased | Primary cell-based high throughput screening assay to identify inhibitors of kruppel-like factor 5 (KLF5) | KLF5 | 290726 | 671 |
| nervousSystem | neurodegeneration | WEE1 | targetBased | Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation | WEE1 | 217959 | 2616 |
| nervousSystem | intellectual developmental disorder with or without epilepsy or cerebellar ataxia | RORA | pathwayBased | Primary Cell-based High Throughput Screening assay for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | 64908 | 278 |
| geneticDisorder | developmental defect during embryogenesis | NR5A1 | targetBased | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | NR5A1 | 64908 | 359 |
| nervousSystem | intellectual developmental disorder with or without epilepsy or cerebellar ataxia | RORA | pathwayBased | Primary Cell-based High Throughput Screening assay for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | 64908 | 979 |
| geneticDisorder | developmental defect during embryogenesis | NR5A1 | targetBased | Primary Cell-based High Throughput Screening assay for activators of the nuclear receptor Steroidogenic Factor 1 (SF-1) | NR5A1 | 64908 | 1225 |
| cancer | neoplastic disease or syndrome | JAK2 | targetBased | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | 217959 | 2390 |
| S1PR4 | targetBased | Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | 217959 | 569 | ||
| S1PR4 | targetBased | Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | 217959 | 771 | ||
| cancer | neoplastic disease or syndrome | NPY2R | targetBased | Primary cell based high-throughput screening assay for antagonists of neuropeptide Y receptor Y2 (NPY-Y2) | NPY2R | 140088 | 1384 |
| psychiatricDisorder | cognitive disorder | HTR1E | targetBased | Primary Cell Based High Throughput Screening Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | 64908 | 641 |
| psychiatricDisorder | cognitive disorder | HTR1E | targetBased | Primary Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | HTR1E | 64908 | 446 |
| nervousSystem | neurodegeneration | VCP | targetBased | Primary biochemical high-throughput screening assay to measure P97 ATPase inhibition | VCP | 217959 | 923 |
| antiViral | HIV | HIV type 1 | targetBased | Primary biochemical high-throughput screening assay for inhibitors of the HIV Rev RRE RNA interaction (disruption of protein-RNA interaction) | REV | 96879 | 769 |
| cancer | neoplastic disease or syndrome | MAPK10 | targetBased | Primary biochemical high-throughput screening assay for inhibitors of the c-Jun N-Terminal Kinase 3 (JNK3) | MAPK10 | 59788 | 366 |
| visualSystem | eye disease | ROCK2 | targetBased | Primary biochemical high-throughput screening assay for inhibitors of Rho kinase 2 (Rhok2) | ROCK2 | 59788 | 212 |
| nervousSystem | neurodegeneration | PTK2 | targetBased | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) | PTK2 | 96879 | 811 |
| antiBacterial | P. aeruginosa | Pseudomonas aeruginosa | targetBased | Primary biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase | BLAVIM-2 | 290726 | 2575 |
| RBBP9 | targetBased | Primary biochemical high throughput screening assay to identify inhibitors of Retinoblastoma binding protein 9 (RBBP9) | RBBP9 | 217959 | 445 | ||
| biologicalProcess | apoptosis | BCL2L1_modulators | targetBased | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). | BCL2L1 | 314998 | 2199 |
| metabolicEndocrine | endocrine pancreas disorder | PPARG | targetBased | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 3 (SRC-3) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | 196177 | 519 |
| metabolicEndocrine | endocrine pancreas disorder | PPARG | targetBased | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | 196176 | 670 |
| metabolicEndocrine | endocrine pancreas disorder | PPARG | targetBased | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | 196177 | 811 |
| nervousSystem | neurodegeneration | PRMT1 | targetBased | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) | PRMT1 | 369953 | 4757 |
| antiBacterial | E. coli | Escherichia coli ΔtolC mutations | phenotypic | Primary Antimicrobial Assay for E. coli BW25113 ∆tolC::kan Protocol for 384-well HTS | 65096 | 1420 | |
| antiViral | Dengue | Dengue virus type 2 | targetBased | Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition | P29991 | 338623 | 1013 |
| antiViral | SARS-CoV | SARS-CoV | pathwayBased | PLP&3CLP proteasesPChem screens plus phenotypic records @ ChEMBL | PLP&3CLP proteases | ||
| antiBacterial | luminous vibriosis | Vibrio harveyi (Beneckea harveyi) | targetBased | Plate Read Microorganism-Based Primary HTS to Identify Modulators of the AI-2 Quorum Sensing System | LUXP | 302177 | 1222 |
| antiMicrobial | malaria | Plasmodium falciparum Dd2 | phenotypic | Plasmodium falciparum Dd2 Sybr green parasite growth Measured in Cell-Based and Microorganism Combination System Using Plate Reader | 93079 | 2144 | |
| antiFungal | fungusGeneral | antifungal efflux pumps inhibitors | phenotypic | Phenotypic HTS multiplex for antifungal efflux pump inhibitors | 328897 | 1437 | |
| antiBacterial | Campylobacter jejuni | Campylobacter jejuni | targetBased | PgID: DNTB colorimetric HTS to detect inhibitor of PgID Measured in Biochemical System Using Plate Reader - 2164-01_Inhibitor_SinglePoint_HTS_Activity | WLAI | 355889 | 350 |
| gastroIntestinal | intestinal disease | OTUD3 | targetBased | OTUD3 deubiquitinase inhibition: Primary qHTS | OTUD3 | 47480 | 334 |
| cancer | cancerGeneral | nrf2Inhibitors | targetBased | Nrf2 qHTS screen for inhibitors | NFE2L2 | 360873 | 7438 |
| cardioVascular | hypertension | sEH_inhibitors | targetBased | Novel sEH inhibitors for the therapeutic treatment of hypertension and inflammation | EPHX2 | 90640 | 310 |
| antiMicrobial | malaria | P. falciparum erythrocyte W2 | phenotypic | NOVARTIS: Inhibition of Plasmodium falciparum W2 (drug-resistant) proliferation in erythrocyte-based infection assay | 5608 | 4612 | |
| antiMicrobial | malaria | P. Falciparum erythrocyte 3D7 | phenotypic | NOVARTIS: Inhibition of Plasmodium falciparum 3D7 (drug-susceptible) proliferation in erythrocyte-based infection assay | 5608 | 4205 | |
| antiViral | Measles | Measles Virus | phenotypic | Non-Nucleoside Inhibitor of Measles Virus RNA-Dependent RNA Polymerase Complex Activity HTS Single Point (MLSMR Library) | 137777 | 2077 | |
| cancer | cancerWithAlterationsInDnaRepair | yeastScreenWithAlterationsInDnaRepair | phenotypic | NCI Yeast Anticancer Drug Screen. Data for the sgs1 mgt1 strain | 80498 | 9555 | |
| cancer | cancerWithAlterationsInDnaRepair | yeastScreenWithAlterationsInDnaRepair | phenotypic | NCI Yeast Anticancer Drug Screen. Data for the rad50 strain | 81133 | 9814 | |
| cancer | cancerWithAlterationsInDnaRepair | yeastScreenWithAlterationsInDnaRepair | phenotypic | NCI Yeast Anticancer Drug Screen. Data for the mlh1 rad18 strain | 81112 | 10175 | |
| cancer | cancerWithAlterationsInDnaRepair | yeastScreenWithAlterationsInDnaRepair | phenotypic | NCI Yeast Anticancer Drug Screen. Data for the mec2-1 strain | 81133 | 8837 | |
| cancer | cancerWithAlterationsInDnaRepair | yeastScreenWithAlterationsInDnaRepair | phenotypic | NCI Yeast Anticancer Drug Screen. Data for the cln2 rad14 strain | 80498 | 8083 | |
| cancer | cancerWithAlterationsInDnaRepair | yeastScreenWithAlterationsInDnaRepair | phenotypic | NCI Yeast Anticancer Drug Screen. Data for the bub3 strain | 80504 | 9618 | |
| cancer | leukemia | leukemia | phenotypic | NCI In Vivo Anticancer Drug Screen. Data for tumor model P388 Leukemia (intraperitoneal) in CD2F1 (CDF1) mice | 44527 | 2353 | |
| cancer | leukemia | leukemia | phenotypic | NCI In Vivo Anticancer Drug Screen. Data for tumor model L1210 Leukemia (intraperitoneal) in B6D2F1 (BDF1) mice | 55741 | 1560 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the UO-31 Renal cell line | 74677 | 3544 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the UO-31 Renal cell line | 52726 | 2935 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the UACC-257 Melanoma cell line | 71797 | 2912 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the UACC-257 Melanoma cell line | 52717 | 2210 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the UACC-62 Melanoma cell line | 74782 | 3675 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the UACC-62 Melanoma cell line | 52399 | 3598 | |
| cancer | glioblastoma | glioblastoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the U251 Central Nervous System cell line | 73184 | 3470 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the U251 Central Nervous System cell line | 53211 | 3544 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the TK-10 Renal cell line | 74445 | 2716 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the TK-10 Renal cell line | 52047 | 1986 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the T-47D Breast cell line | 72767 | 3276 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the T-47D Breast cell line | 38148 | 2490 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SW-620 Colon cell line | 75327 | 3576 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SW-620 Colon cell line | 53508 | 4024 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SR Leukemia cell line | 67113 | 5428 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SR Leukemia cell line | 44307 | 5398 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SNB-75 Central Nervous System cell line | 73093 | 3359 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SNB-75 Central Nervous System cell line | 49685 | 3444 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SNB-19 Central Nervous System cell line | 74208 | 1576 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SNB-19 Central Nervous System cell line | 52778 | 2515 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SN12C Renal cell line | 74708 | 2495 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SN12C Renal cell line | 52967 | 3005 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-OV-3 Ovarian cell line | 73297 | 2087 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-OV-3 Ovarian cell line | 51081 | 2532 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-28 Melanoma cell line | 74869 | 2694 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-28 Melanoma cell line | 52593 | 1983 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-5 Melanoma cell line | 73327 | 4240 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-5 Melanoma cell line | 52438 | 3585 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-2 Melanoma cell line | 70939 | 2926 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-2 Melanoma cell line | 50295 | 2412 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SF-539 Central Nervous System cell line | 74520 | 4513 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SF-539 Central Nervous System cell line | 50511 | 3547 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SF-295 Central Nervous System cell line | 72353 | 3611 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SF-295 Central Nervous System cell line | 53205 | 3526 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SF-268 Central Nervous System cell line | 75289 | 2115 | |
| cancer | CNS_tumor | CNS_tumor | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the SF-268 Central Nervous System cell line | 52931 | 2856 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the RXF 393 Renal cell line | 71215 | 4339 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the RXF 393 Renal cell line | 48061 | 3402 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the RPMI-8226 Leukemia cell line | 70780 | 4886 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the RPMI-8226 Leukemia cell line | 49781 | 4206 | |
| cancer | prostateCancer | prostateCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the PC-3 Prostate cell line | 73700 | 2603 | |
| cancer | prostateCancer | prostateCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the PC-3 Prostate cell line | 40498 | 3034 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-8 Ovarian cell line | 74586 | 2891 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-8 Ovarian cell line | 53426 | 3114 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-5 Ovarian cell line | 75004 | 1854 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-5 Ovarian cell line | 52502 | 2104 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-4 Ovarian cell line | 73088 | 2443 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-4 Ovarian cell line | 50969 | 2336 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-3 Ovarian cell line | 74864 | 4915 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the OVCAR-3 Ovarian cell line | 51983 | 3749 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI/ADR-RES Breast cell line | 74972 | 2944 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI/ADR-RES Breast cell line | 40779 | 2492 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H522 Non-Small Cell Lung cell line, single concentration | 71275 | 5229 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H522 Non-Small Cell Lung cell line | 48987 | 4260 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H460 Non-Small Cell Lung cell line, single concentration | 75211 | 4608 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H460 Non-Small Cell Lung cell line | 52033 | 4098 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H322M Non-Small Cell Lung cell line, single concentration | 73050 | 1747 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H322M Non-Small Cell Lung cell line | 52046 | 2317 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H226 Non-Small Cell Lung cell line, single concentration | 72375 | 2184 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H226 Non-Small Cell Lung cell line | 49564 | 2467 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H23 Non-Small Cell Lung cell line, single concentration | 75010 | 2580 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the NCI-H23 Non-Small Cell Lung cell line | 53214 | 3094 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MOLT-4 Leukemia cell line | 73777 | 4676 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MOLT-4 Leukemia cell line | 52219 | 4310 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MDA-MB-435 Breast cell line | 75071 | 5500 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MDA-MB-435 Breast cell line | 40193 | 3548 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MDA-MB-231/ATCC Breast cell line | 74706 | 3330 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MDA-MB-231/ATCC Breast cell line | 40090 | 2464 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MCF7 Breast cell line | 75981 | 4212 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MCF7 Breast cell line | 40400 | 4425 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MALME-3M Melanoma cell line | 71882 | 3760 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the MALME-3M Melanoma cell line | 49416 | 2812 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the M14 Melanoma cell line | 73968 | 4221 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the M14 Melanoma cell line | 52257 | 3432 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the LOX IMVI Melanoma cell line | 73462 | 4776 | |
| cancer | melanoma | melanoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the LOX IMVI Melanoma cell line | 50080 | 3993 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the KM12 Colon cell line | 75218 | 3369 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the KM12 Colon cell line | 53104 | 3462 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the K-562 Leukemia cell line | 71880 | 4980 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the K-562 Leukemia cell line | 51855 | 4709 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the IGROV1 Ovarian cell line | 72867 | 3166 | |
| cancer | ovarianCancer | ovarianCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the IGROV1 Ovarian cell line | 52609 | 3249 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HT29 Colon cell line | 74688 | 5101 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HT29 Colon cell line | 52844 | 3773 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HS 578T Breast cell line | 71841 | 2560 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HS 578T Breast cell line | 38502 | 2659 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HOP-92 Non-Small Cell Lung cell line | 65189 | 3616 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HOP-92 Non-Small Cell Lung cell line | 47537 | 3298 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HOP-62 Non-Small Cell Lung cell line | 73643 | 2556 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HOP-62 Non-Small Cell Lung cell line | 52001 | 2981 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HL-60(TB) Leukemia cell line | 71675 | 5995 | |
| cancer | leukemia | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HL-60(TB) Leukemia cell line | 48426 | 4751 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HCT-116 Colon cell line | 75551 | 5013 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HCT-116 Colon cell line | 52727 | 4422 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HCT-15 Colon cell line | 75530 | 3437 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HCT-15 Colon cell line | 53050 | 3475 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HCC-2998 Colon cell line | 72852 | 3007 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the HCC-2998 Colon cell line | 48421 | 2752 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the EKVX Non-Small Cell Lung cell line, single concentration | 64389 | 1626 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the EKVX Non-Small Cell Lung cell line | 50820 | 2137 | |
| cancer | prostateCancer | prostateCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the DU-145 Prostate cell line | 74776 | 2861 | |
| cancer | prostateCancer | prostateCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the DU-145 Prostate cell line | 40598 | 2824 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the COLO 205 Colon cell line | 72743 | 4943 | |
| cancer | colonCancer | colonCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the COLO 205 Colon cell line | 52712 | 3480 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the CCRF-CEM Leukemia cell line | 70489 | 4627 | |
| cancer | leukemia | leukemia | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the CCRF-CEM Leukemia cell line | 50580 | 5047 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the CAKI-1 Renal cell line | 68322 | 2874 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the CAKI-1 Renal cell line | 50188 | 3283 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the BT-549 Breast cell line | 71655 | 2694 | |
| cancer | breastCancer | breastCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the BT-549 Breast cell line | 37232 | 2330 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the ACHN Renal cell line | 74545 | 3244 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the ACHN Renal cell line | 52894 | 3233 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the A549/ATCC Non-Small Cell Lung cell line, single concentration | 74386 | 2485 | |
| cancer | nonSmallCellLungCarcinoma | nonSmallCellLungCarcinoma | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the A549/ATCC Non-Small Cell Lung cell line | 53560 | 2992 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the A498 Renal cell line | 69851 | 3516 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the A498 Renal cell line | 47090 | 3449 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the 786-0 Renal cell line | 74688 | 3319 | |
| cancer | renalCancer | renalCancer | phenotypic | NCI human tumor cell line growth inhibition assay. Data for the 786-0 Renal cell line | 52428 | 3081 | |
| antiViral | HIV | HIV type 1 | phenotypic | NCI AIDS Antiviral Assay | 41976 | 1527 | |
| cardioVascular | congestive heart failure | NPR1 | targetBased | Natriuretic polypeptide receptor (hNpr1) antagonism - Primary qHTS | NPR1 | 76168 | 1231 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis | targetBased | Mycobacterium tuberculosis BioA enzyme inhibitor Measured in Biochemical System Using Plate Reader - 2163-01_Inhibitor_SinglePoint_HTS_Activity | BioA | 353572 | 342 |
| otherPhenotypes | circadian rhythm | RGS16 | targetBased | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | RGS16 | 218528 | 826 |
| nervousSystem | Mendelian neurodevelopmental disorder | GNAO1 | targetBased | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | GNAO1 | 218528 | 750 |
| nervousSystem | Mendelian neurodevelopmental disorder | GNAO1 | targetBased | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. | GNAO1 | 218528 | 770 |
| nervousSystem | Mendelian neurodevelopmental disorder | GNAO1 | targetBased | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | GNAO1 | 218528 | 711 |
| biologicalProcess | apoptosis | BCL2A1_modulators | targetBased | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1 | BCL2A1 | 194826 | 237 |
| RPL19B | pathwayBased | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ RPL19A_MLPCN. | RPL19B | 325372 | 982 | ||
| MEP2 | pathwayBased | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ MEP2_MLPCN. | MEP2 | 326651 | 1682 | ||
| cancer | cancerGeneral | mTOR_pathwayModulators | pathwayBased | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ LAP4_MLPCN. | APE1 | 324734 | 1090 |
| cancer | cancerGeneral | mTOR_pathwayModulators | pathwayBased | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ CIT2_MLPCN. | CIT2 | 321534 | 210 |
| cancer | neoplastic disease or syndrome | MAP3K3 | targetBased | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | MAP3K3 | 289573 | 4159 |
| nervousSystem | neurodegeneration | MAP4K2 | targetBased | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase 2 mutant | MAP4K2 | 289539 | 1003 |
| nervousSystem | neurodegeneration | MAP4K2 | targetBased | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype | MAP4K2 | 289465 | 3276 |
| immune | autoimmuneDisorders | cGAS_inhibitors | targetBased | mouse cGAS RapidFire screen | CGAS | 123258 | 226 |
| immune | autoimmuneDisorders | cGAS_inhibitors | targetBased | mouse cGAS chemiluminescence screen | CGAS | 160326 | 237 |
| reproductiveSystem | male reproductive system disease | PTGER2 | targetBased | Modulators of the EP2 prostaglandin E2 receptor - Primary Screening | PTGER2 | 255537 | 2141 |
| biologicalProcess | secretionPath | Modulators of Post-Golgi Transport | phenotypic | Modulators of Post-Golgi Transport | 97509 | 875 | |
| nervousSystem | epilepsy | AMPAStargazinComplexModulators | targetBased | Modulation of AMPAR-stargazin complexes | CACNG2 | 40473 | 1400 |
| antiBacterial | S. Pneumoniae | Streptococcus pyogenes serotype M1 | targetBased | MLPCN Streptokinase Expression Inhibition | SKA | 303477 | 3959 |
| SIRT5 | targetBased | MLPCN SirT-5 Measured in Biochemical System Using Imaging - 7044-01_Inhibitor_SinglePoint_HTS_Activity_Set5 | SIRT5 | 323507 | 3752 | ||
| hematologic | thrombosis | plateletActivationInhibitors | phenotypic | MLPCN Platelet Activation -Dense Granule Release | 302451 | 661 | |
| biologicalProcess | Oxidative Metabolic Function | PGC1aInhibitors | phenotypic | MLPCN PGC1a Modulators Measured in Cell-Based System Using Plate Reader - 2139-01_Inhibitor_SinglePoint_HTS_Activity | 345870 | 601 | |
| biologicalProcess | Oxidative Metabolic Function | PGC1aActivators | phenotypic | MLPCN PGC1a Modulators Measured in Cell-Based System Using Plate Reader - 2139-01_Activator_SinglePoint_HTS_Activity | 345870 | 740 | |
| MEX-5 | targetBased | MLPCN maternal gene expression-MEX-5 TCR-2 binding assay-Primary Screen | MEX-5 | 301788 | 1137 | ||
| immune | autoimmuneDisorders | ERAP1_inhibitors | targetBased | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity | ERAP1 | 335777 | 499 |
| nervousSystem | PD | aSynucleinExpressionInhibitors | phenotypic | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors | 303801 | 2498 | |
| biologicalProcess | synucleinEffect | aSynucleinExpressionActivators | phenotypic | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators | 303801 | 21690 | |
| cancer | neoplastic disease or syndrome | MITF | targetBased | MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Inhibitor_SinglePoint_HTS_Activity | MITF | 331360 | 2760 |
| cancer | melanoma | MITF_expressionEnhancers | phenotypic | MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint_HTS_Activity | 300845 | 2272 | |
| metabolicEndocrine | endocrine pancreas disorder | PPARG | targetBased | Measurement of TR-FRET detection format artefact in the screen for agonists of steroid receptor coactivator 3 (SRC-3) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | 99314 | 390 |
| metabolicEndocrine | endocrine pancreas disorder | PPARG | targetBased | Measurement of TR-FRET detection format artefact in the screen for agonists of steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | 196176 | 782 |
| metabolicEndocrine | endocrine pancreas disorder | PPARG | targetBased | Measurement of TR-FRET detection format artefact in the screen for agonists of steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | PPARG | 99314 | 335 |
| muculoEskeletalConnective | bone disease | MMP14 | targetBased | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription | MMP14 | 86733 | 537 |
| metabolicEndocrine | T2diabetes | Glucose-dependent insulin secretion | phenotypic | Luminescent GLuc Reporter Gene Assay Primary HTS to Identify Small Molecule Activator of Glucose Dependent Insulin Secretion Measured in Cell-Based System Using Plate Reader - 7055-01_Activator_SinglePoint_HTS_Activity | 371108 | 2287 | |
| metabolicEndocrine | cholesterolLevels | ALPI_activators | targetBased | Luminescent assay for identification of activators of bovine intestinal alkaline phosphatase | ALPI | 195570 | 326 |
| immune | immunomodulation | ALPG_activators | targetBased | Luminescent assay for HTS discovery of chemical activators of placental alkaline phosphatase | ALPG | 95729 | 1178 |
| nervousSystem | palsy | NR0B1 | targetBased | Luminescence-based primary cell-based high throughput screening assay to identify inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1) | NR0B1 | 343468 | 3417 |
| immune | immunomodulation | AHR_activators | targetBased | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | AHR | 324747 | 7988 |
| cancer | cancerGeneral | HSP90AA1 | targetBased | Luminescence-based primary biochemical high throughput screening assay to identify inhibitors of the Heat Shock Protein 90 (HSP90) | HSP90AA1 | 290726 | 2649 |
| cancer | neoplastic disease or syndrome | NR5A2 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) | NR5A2 | 363803 | 458 |
| cancer | neoplastic disease or syndrome | OPRM1 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | 335239 | 695 |
| NCOA3 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3) | NCOA3 | 359207 | 620 | ||
| cancer | neoplastic disease or syndrome | NCOA2 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) | NCOA2 | 368927 | 620 |
| cancer | neoplastic disease or syndrome | NCOA1 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) | NCOA1 | 359206 | 428 |
| metabolicEndocrine | insulinSensitization | NR2F2 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of COUP-TFII (NR2F2) | NR2F2 | 369953 | 2602 |
| metabolicEndocrine | Energy balance, obesity | MC4R | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | MC4R | 356160 | 3470 |
| psychiatricDisorder | developmental disorder of mental health | HTR2A | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | 363803 | 2412 |
| antiHelminthic | H. glycines | DAF-12_activators | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify agonists of the DAF-12 from the parasite H. glycines (hgDAF-12). | DAF-12 | 369953 | 6837 |
| cancer | neoplastic disease or syndrome | OPRM1 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | OPRM1 | 335239 | 991 |
| nervousSystem | neurodegeneration | HEL111 | pathwayBased | Luminescence-based cell-based primary high throughput screening assay to identify activators of Transthyretin (TTR) transcription | HEL111 | 91909 | 1155 |
| muculoEskeletalConnective | Friedreich ataxia | FXN | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify activators of the GAA850 frataxin (FXN) promoter | FXN | 356160 | 1985 |
| geneticDisorder | Rare genetic developmental defect during embryogenesis | SMARCA2 | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) | SMARCA2 | 368927 | 3838 |
| antiHelminthic | S. stercoralis | DAF-12_activators | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify activators of the DAF-12 from the parasite S. stercoralis (ssDAF-12) | DAF-12 | 369953 | 3700 |
| antiHelminthic | H. contortus | DAF-12_activators | targetBased | Luminescence-based cell-based primary high throughput screening assay to identify activators of the DAF-12 from the parasite H. contortus (hcDAF-12) | DAF-12 | 369953 | 5353 |
| nervousSystem | palsy | NR0B1 | targetBased | Luminescence-based cell-based primary high throughput screening assay for inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1): repression of SF-1 (NR5A1) activated StAR promoter by full-length DAX-1 | NR0B1 | 368927 | 4094 |
| nervousSystem | neurodegeneration | NR2E3 | targetBased | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | NR2E3 | 362026 | 1281 |
| antiMicrobial | trypanosomiasis | met-tRNA synt | targetBased | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | 3662741 | 363803 | 1456 |
| metabolicEndocrine | obesity, diabetes, and cardiovascular disease | PLIN5 | targetBased | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) | PLIN5 | 363803 | 2851 |
| STK33 | targetBased | Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of Serine/Threonine Kinase 33 Activity | STK33 | 321808 | 235 | ||
| psychiatricDisorder | mental or behavioural disorder | GSK3A | targetBased | Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | GSK3A | 315412 | 318 |
| antiMicrobial | chagas | T. Cruzi replication | phenotypic | Luminescence Cell-Based/Microorganism Primary HTS to Identify Inhibitors of T.Cruzi Replication | 303218 | 4394 | |
| cardioVascular | ischemia | HIF_expressionActivators | phenotypic | Luminescence Cell-Based Primary HTS to Identify Transcriptional Activators of Hypoxia-Inducible Factor Pathway | 300341 | 950 | |
| cancer | EwingSarcoma | EWS/Fli transcriptional activity inhibitors | phenotypic | Luminescence Cell-Based Primary HTS to identify inhibitors of the oncoprotein EWS/Fli transcriptional activity Measured in Cell-Based System Using Plate Reader - 7014-01_Inhibitor_SinglePoint_HTS_Activity | 342236 | 2318 | |
| STK33 | targetBased | Luminescence Cell-Based Primary HTS to Identify Inhibitors of STK33 | STK33 | 37341 | 2812 | ||
| cancer | neoplastic disease or syndrome | HSF1 | targetBased | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1). | HSF1 | 301324 | 2328 |
| cancer | breastCancer | breastCancerStemCellsCadherinNull | phenotypic | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Cancer Stem Cells | 300621 | 3187 | |
| metabolicEndocrine | T1Diabetes | b cell apoptosis | phenotypic | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Beta Cell Apoptosis. | 303500 | 2435 | |
| biologicalProcess | apoptosis | BCL2L11_inhibitors | targetBased | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | BCL2L11 | 325630 | 216 |
| geneticDisorder | Rare genetic developmental defect during embryogenesis | YAP1 | targetBased | Luminescence cell-based high throughput primary assay to identify inhibitors of TEAD-YAP interaction. | YAP1 | 639428 | 9218 |
| biologicalProcess | SUMOylation | SUMOylationInhibitors | phenotypic | Luminescence Microorganism Primary HTS to Identify Inhibitors of the SUMOylation Pathway Using a Temperature Sensitive Growth Reversal Mutant Mot1-301 | 318458 | 3322 | |
| cancer | cancerGeneral | NLG_inhibitors | phenotypic | Luciferase Reporter Cell Based HTS to identify inhibitors of N-linked Glycosylation Measured in Cell-Based System Using Plate Reader - 2146-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | 358025 | 830 | |
| antiMicrobial | leishmaniasis | Leishmania promastigote | phenotypic | Leishmania major promastigote HTS | 196141 | 17620 | |
| cancer | neoplastic disease or syndrome | KLK5 | targetBased | Kallikrein 5 1536 HTS | KLK5 | 214187 | 1264 |
| cancer | cancerGeneral | Her-Kinase Expression | phenotypic | Isolation of Inhibitors of Her-Kinase Expression - 66K library screen | 64629 | 448 | |
| metabolicEndocrine | thyroid disease | TSHR | targetBased | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | TSHR | 329153 | 670 |
| antiBacterial | plague | Yersinia pestis | targetBased | Inhibitors of Y. pestis Topo-I using cleavage product accumulation Measured in Biochemical System Using Plate Reader - 2123-01_Inhibitor_SinglePoint_HTS_Activity | SUPX | 356253 | 229 |
| nervousSystem | neurodegeneration | USP1 | targetBased | Inhibitors of USP1/UAF1: Primary Screen | USP1 | 389569 | 904 |
| metabolicEndocrine | nutritional deficiency disease | VDR | targetBased | Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | 394050 | 3624 |
| reproductiveSystem | male reproductive system disease | PTGER2 | targetBased | Inhibitors of the EP2 Prostaglandin E2 Receptor - Primary Screen | PTGER2 | 250190 | 1304 |
| antiPrion | prionDisease | PrP_Inhibitors | phenotypic | Inhibitors of Prion Protein 5' UTR mRNA Measured in Cell-Based System Using Plate Reader - 2078-01_Inhibitor_SinglePoint_HTS_Activity | 334634 | 1167 | |
| antiMicrobial | malaria | Plasmodium falciparum (isolate 3D7) | targetBased | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | LAP | 216988 | 827 |
| antiMicrobial | malaria | Plasmodium falciparum (isolate 3D7) | targetBased | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) | M1AAP | 216987 | 913 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | targetBased | Inhibitors of Mycobacterial Glucosamine-1-phosphate acetyl transferase (GlmU) | GLMU | 215860 | 533 |
| antiViral | EBV | Epstein-Barr virus | phenotypic | Inhibitors of Epstein-Barr LMP1 inducible NF-kappaB luciferase reporter Measured in Cell-Based System Using Plate Reader - 2122-01_Inhibitor_SinglePoint_HTS_Activity | LMP1 | 345064 | 2373 |
| cancer | cancerGeneral | Inhibitors of CDC25B-CDK2/CyclinA interaction | targetBased | Inhibitors of CDC25B-CDK2/CyclinA interaction | CCNA2 | 93798 | 679 |
| nervousSystem | epilepsy | CACNA1H_inhibitors | targetBased | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H | 104728 | 4230 |
| cancer | cancerGeneral | TROY_signalling_inhibitors | phenotypic | Inhibitor identification of TROY dependent signaling using uHTS single point assay | 360657 | 3551 | |
| cancer | neoplastic disease or syndrome | MLLT3 | targetBased | Inhibition of the MLL-AF4-AF9 Interaction in Pediatric Leukemia Measured in Biochemical System Using Plate Reader - 2160-01_Inhibitor_SinglePoint_HTS_Activity | MLLT3 | 344459 | 1627 |
| antiMicrobial | trypanosomiasis | Trypanosoma cruzi | phenotypic | Inhibition of T.cruzi proliferation in culture Measured in Cell-Based System Using Plate Reader - 2138-01_Inhibitor_SinglePoint_HTS_Activity | 76537 | 4582 | |
| antiMicrobial | malaria | P. falciparum LDH | phenotypic | Inhibition of P. falciparum LDH | 13456 | 0 | |
| antiMicrobial | malaria | P. falciparum Dd2 | phenotypic | Inhibition of P. falciparum Dd2 | 13456 | 7921 | |
| antiMicrobial | malaria | P. falciparum 3d7 | phenotypic | Inhibition of P. falciparum 3D7 | 13456 | 13456 | |
| immune | fibrosis | fibronectinDeposition | phenotypic | Inhibition of Alexa 488-Fibronectin deposition #on AH1F cell monolayers Measured in Cell-Based System Using Plate Reader - 7059-01_Inhibitor_SinglePoint_HTS_Activity | 342865 | 297 | |
| antiMicrobial | malaria | Plasmodium falciparum (isolate 3D7) | phenotypic | In vivo-based yeast HTS to detect compounds rescuing yeast growth/survival of Plasmodium Falciparum HSP40-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-01_Inhibitor_SinglePoint_HTS_Activity | 811941 | 336519 | 2306 |
| cancer | neoplastic disease or syndrome | GPR55 | targetBased | Image-Based HTS for Selective Antagonists for GPR55 | GPR55 | 291657 | 370 |
| cancer | neoplastic disease or syndrome | NTSR1 | targetBased | Image-Based HTS for Selective Agonists for NTR1 | NTSR1 | 331753 | 556 |
| immune | immunomodulation | NFkB_Translocation_inhibitors | phenotypic | IL-1B Induced NFkB Translocation - Primary Screen | 94265 | 409 | |
| metabolicEndocrine | congenitalDiabetes | HNF4_binding_to_DNA_enhancers | targetBased | Identify inhibitors of HNF4 alpha protein binding to DNA | NR2A1 | 363839 | 1098 |
| antiViral | HIV | HIV type 1 | targetBased | Identification of VIF Inhibitors Measured in Cell-Based System Using Imaging - 2108-01_Inhibitor_SinglePoint_HTS_Activity | VIF | 335681 | 1162 |
| antiViral | SV40 | Simian virus 40 (SV40) | targetBased | Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents | P03070 | 305355 | 1203 |
| rareDiseases | cysticFibrosis | cftrCorrectors | targetBased | Identification of Small Molecule Correctors of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Delta508 Mutation Function in Human Bronchial Epithelial Cells. Measured in Cell-Based System Using Plate Reader - 7017-01_Other_SinglePoint_HTS_Activity | CFTR | 343786 | 1253 |
| nervousSystem | monogenic epilepsy | SLC12A5 | targetBased | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Primary Screen | SLC12A5 | 189132 | 4127 |
| geneticDisorder | Pseudoxanthoma elasticum | ABCC1_activators | targetBased | Identification of Molecular Probes that Activate MRP-1 | ABCC1 | 138717 | 842 |
| cancer | neoplastic disease or syndrome | RAD54L | targetBased | Identification of inhibitors of RAD54 Measured in Biochemical System Using Plate Reader - 2159-01_Inhibitor_SinglePoint_HTS_Activity | RAD54L | 358498 | 505 |
| cancer | cancerGeneral | Chromobox protein homolog 7 inhibitors | targetBased | Identification of CBX7 inhibitors - Primary Alpha Screen | CBX7 | 64999 | 724 |
| cancer | neoplastic disease or syndrome | SELE | targetBased | Identification of agents that induce E-selectin on human endothelial cells Measured in Cell-Based System Using Imaging - 2152-01_Activator_SinglePoint_HTS_Activity | SELE | 257988 | 963 |
| SDO1 | targetBased | Identification and characterization of compounds for addressing human bone marrow failure | SDO1 | 138737 | 298 | ||
| biologicalProcess | angiogenesis | angiogenesis_modulators_secondary | phenotypic | Human Lung Fibroblast Proliferation Assay | 84879 | 937 | |
| cancer | smallCellLungCarcinoma | smallCellLungCarcinomaCellLineExpressingTransportDetoxProtMDR1 | phenotypic | Human H69AR Lung Tumor Cell Growth Inhibition Assay - 86K Screen | 85200 | 5142 | |
| biologicalProcess | angiogenesis | angiogenesis_modulators | phenotypic | Human Endothelial Cell Proliferation Assay in 384-well format | 86159 | 925 | |
| immune | autoimmuneDisorders | cGAS_inhibitors | targetBased | human cGAS chemiluminescence screen | CGAS | 281243 | 218 |
| immune | fibrosis | ALR activators | targetBased | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS | GFER | 288728 | 10857 |
| cancer | cancer | ALR inhibitors | targetBased | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS | GFER | 288728 | 10857 |
| biologicalProcess | Lipid transport | SCARB1 | targetBased | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Inhibitor_SinglePoint_HTS_Activity | SCARB1 | 319204 | 3065 |
| SCARB1 | targetBased | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity | SCARB1 | 316970 | 306 | ||
| cancer | neoplastic disease or syndrome | HRAS | targetBased | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | HRAS | 194628 | 267 |
| cancer | neoplastic disease or syndrome | RAC1 | targetBased | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac wildtype | RAC1 | 194628 | 521 |
| cancer | neoplastic disease or syndrome | RAC1 | targetBased | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac activated mutant | RAC1 | 194629 | 219 |
| RAB2A | targetBased | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype | RAB2A | 194628 | 365 | ||
| biologicalProcess | RAS_pathways | RAS_inhibitors | phenotypic | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype | 194628 | 398 | |
| biologicalProcess | necrosis | necrosisByCaspaseInhibitors | phenotypic | HTS to identify inhibitors of zVAD Induced Cell Death in L929 Cells. | 217101 | 832 | |
| cancer | leukemia | HOXA9 | pathwayBased | HTS to identify compounds that promote myeloid differentiation with MLPCN compound set | HOXA9 | 358556 | 3721 |
| immune | pemphigus | pemphigusAntibodiesInhibitors | phenotypic | HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies | 311344 | 1495 | |
| antiFungal | antifungal | VMA11 | targetBased | HTS of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin | VMA11 | 345985 | 1287 |
| immune | fibrosis | SMAD3 | targetBased | HTS of Smad transcription factor inhibitors | SMAD3 | 88033 | 251 |
| reproductiveSystem | menopauseSymptoms | ESR1_modulators | targetBased | HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1 | 86095 | 1151 |
| cancer | breastCancer | ESR1_inhibitors | targetBased | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1 | 86095 | 1442 |
| cancer | neoplastic disease or syndrome | SENP8 | targetBased | HTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 8 (SENP8) | SENP8 | 330392 | 4119 |
| immune | immune deficiency disease | ITGB2 | targetBased | HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | 92518 | 501 |
| metabolicEndocrine | disorder of glycosylation | MPI | targetBased | HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | MPI | 194152 | 814 |
| metabolicEndocrine | disorder of glycosylation | MPI | targetBased | HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate | MPI | 194152 | 1288 |
| metabolicEndocrine | disorder of glycosylation | MPI | targetBased | HTS identification of compounds activating phosphomannose isomerase (PMI) via a fluorescence intensity assay using a near- saturating concentration of mannose 6-phosphat | MPI | 194152 | 656 |
| cancer | cancerGeneral | HSP90 known inhibitor displacement | targetBased | HTS for Tumor Hsp90 Inhibitors | HSP90AA1 | 63696 | 220 |
| antiMicrobial | cryptococcosis | Cryptococcus neoformans | targetBased | HTS for the detection of C. neoformans cell lysis via adenylate kinase (AK) release Measured in Microorganism System Using Plate Reader - 2162-01_Inhibitor_SinglePoint_HTS_Activity | AK | 357997 | 735 |
| muculoEskeletalConnective | myotoxicity | C2C12_myopathy | phenotypic | HTS for suppressors of simvastatin-induced mytoxicity in differentiated C2C12 cells Measured in Cell-Based System Using Plate Reader - 2112-01_Suppressor_SinglePoint_HTS_Activity | 329274 | 2586 | |
| biologicalProcess | apoptosis | DDIT3_inhibitors | targetBased | HTS for small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress | DDIT3 | 218654 | 8241 |
| metabolicEndocrine | thyroid disease | PAX8 | targetBased | HTS for PAX8 inhibitors using PAX8 luciferase reporter gene assay in RMG-I cells Measured in Cell-Based System Using Plate Reader - 7054-01_Inhibitor_SinglePoint_HTS_Activity | PAX8 | 353950 | 4145 |
| nervousSystem | neurodegeneration | HP1-betaChromodomainInteractionsInhibitors | targetBased | HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails | CBX1 | 383363 | 2142 |
| muculoEskeletalConnective | muscularDystrophy | DUX4_inhibitors | targetBased | HTS for inhibitors of DUX4-mediated transcriptional activation | DUX4 | 36365 | 289 |
| cardioVascular | hypertension | CACNA1D_inhibitors | targetBased | HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D | 335531 | 328 |
| gastroIntestinal | intestinal disease | ITGA4 | targetBased | HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | 326888 | 645 |
| cancer | breastCancer | ESR2_inhibitors | targetBased | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2 | 86095 | 1114 |
| dermatology | skin disease | ITGAL | targetBased | HTS for developing T Cell Immune Modulators | ITGAL | 326271 | 221 |
| immune | asthma | ADRB2_activators | targetBased | HTS for Beta-2AR agonists via FAP method | ADRB2 | 339297 | 1446 |
| cancer | cancerGeneral | BAP1_inhibitors | targetBased | HTS for BAP1 Enzyme inhibitors | BAP1 | 71016 | 346 |
| antiBacterial | E. coli | Escherichia coli ribosomal RNAs | phenotypic | HTS for Bacterial rRNA inhibitors Measured in Microorganism-Based System Using Plate Reader - 7056-01_Inhibitor_SinglePoint_HTS_Activity | 348128 | 5500 | |
| nervousSystem | monogenic epilepsy | YWHAG | targetBased | HTS for 14-3-3 protein interaction modulators | YWHAG | 157962 | 312 |
| PTPN7 | targetBased | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target | PTPN7 | 112381 | 724 | ||
| cancer | cancerGeneral | VHR1_inhibitors | targetBased | HTS Colorimetric assay for the identification of compounds that inhibit VHR1 | DUSP3 | 49813 | 347 |
| nervousSystem | PD | D2_PAMs | targetBased | HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | DRD2 | 339887 | 1178 |
| cancer | cancerGeneral | PPP1R15A | targetBased | HTS Assay for Peg3 Promoter Inhibitors | PPP1R15A | 359244 | 6145 |
| antiMicrobial | trypanosomiasis | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | targetBased | HTS assay for inhibitors of Trypanosoma brucei hexokinase 1 | 3663016 | 220222 | 239 |
| cancer | cancerGeneral | AKT1_inhibitors | targetBased | HTS Assay for Inhibitors of Akt Phophorylation: Primary Screen | AKT1 | 356517 | 1139 |
| metabolicEndocrine | Abnormality of metabolism/homeostasis | TRPV1 | targetBased | HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | 316642 | 617 |
| nervousSystem | psychosis | D2_antagonists | targetBased | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | DRD2 | 336308 | 6862 |
| nervousSystem | PD | D2_agonists | targetBased | HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | DRD2 | 335652 | 1779 |
| biologicalProcess | cytochromesRoles | CYP2C9_activators | targetBased | HTS Assay for Activators of Cytochrome P450 2A9 | CYP2C9 | 95858 | 1368 |
| nervousSystem | pain | CACNA1B_modulators | targetBased | Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | CACNA1B | 292323 | 567 |
| antiViral | HIV | HIV type 1 | targetBased | HIV1_TAR : FRET assay measuring displacement of FAM and TAMRA-labeled Tat peptide from HIV-1 TAR RNA. | TAR | 103073 | 615 |
| antiViral | HIV | HIV type 1 | targetBased | HIV-1 RT-RNase H MLSCN HTS MH077605 | GAG-POL | 65218 | 1250 |
| antiViral | HIV | HIV type 1 | targetBased | HIV-1 RNase H Inhibition | GAG-POL | 99768 | 769 |
| antiViral | HIV | HIV fussion | phenotypic | HIV entry: Env-mediated Cell Fusion Measured in Cell-Based System Using Plate Reader - 7013-01_Inhibitor_SinglePoint_HTS_Activity | 354822 | 3866 | |
| cardioVascular | myocardialFibrosis | GC-B_PAMs | phenotypic | High-throughput screening primary assay to identify small molecule activators of human guanylyl cyclase B (GC-B) receptor activity | 370293 | 399 | |
| cardioVascular | hypertension | GC-A_PAMs | phenotypic | High-throughput screening primary assay to identify small molecule activators of human GC-A enzyme activity | 370293 | 519 | |
| nervousSystem | hearing disorder | MARVELD2 | targetBased | High-Throughput Screening for Modulators of Cytosolic Chaperonin Activity | MARVELD2 | 362274 | 1085 |
| geneticDisorder | ear malformation | GNAI3 | targetBased | High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i G protein subunits | GNAI3 | 204125 | 876 |
| antiBacterial | anthrax | Bacillus anthracis Lethal factor inhibitors | targetBased | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | P15917 | 354794 | 422 |
| antiBacterial | botulism | Clostridium botulinum toxin inhibitors | targetBased | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | BoNT/F | 354794 | 780 |
| antiBacterial | botulism | Clostridium botulinum (strain Hall / ATCC 3502 / NCTC 13319 / Type A) | targetBased | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | BOTA | 354794 | 609 |
| biologicalProcess | autophagy | autophagy imaging assay | phenotypic | High-content cell-based screening for modulators of autophagy | 194528 | 1903 | |
| urinarySystem | focal segmental glomerulosclerosis | TRPC6 | targetBased | High throughput screening of inhibitors of transient receptor potential cation channel C6 (TRPC6) | TRPC6 | 305610 | 3253 |
| urinarySystem | focal segmental glomerulosclerosis | TRPC6 | targetBased | High throughput screening of activators of transient receptor potential cation channel C6 (TRPC6) | TRPC6 | 305610 | 382 |
| antiViral | FMDV | Foot-and-mouth disease virus | phenotypic | High Throughput Screening for Foot and Mouth Disease Virus Antivirals | 404062 | 5020 | |
| psychiatricDisorder | drug addiction | SLC6A3 | targetBased | High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | 108286 | 1415 |
| antiBacterial | tuberculosis | Mycobacterium Tuberculosis | phenotypic | High Throughput Screening Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in 7H9 Media | 327558 | 1938 | |
| antiViral | HIV | HIV-VIF | targetBased | High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradation of Human APOBEC3G:#A time-resolved fluorescence resonance energy transfer (TR-FRET) assay for HIV-1 Vif-APOBEC3G interaction | VIF | 258750 | 1498 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis H37Rv | phenotypic | High Throughput Screen to Identify Inhibitors of Mycobacterium tuberculosis H37Rv | 215098 | 2044 | |
| cancer | colonCancer | colonCancerNotExpressingOncogenicBetaCatenin | phenotypic | High Throughput Screen to Identify Compounds that Suppress the Growth of Human Colon Tumor Cells Lacking Oncogenic Beta Catenin Expression | 138737 | 2051 | |
| cancer | colonCancer | colonCancerwithPtenDeletion | phenotypic | High Throughput Screen to Identify Compounds that Suppress the Growth of Cells with a Deletion of the PTEN Tumor Suppressor | 138417 | 1658 | |
| antiBacterial | Enterococcus faecalis | Enterococcus faecalis (Streptococcus faecalis) | targetBased | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Primary Screen | MVAE | 194344 | 792 |
| nervousSystem | neurodegeneration | NFKB1 | pathwayBased | High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | 193265 | 3100 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis H37Rv | phenotypic | High Throughput Screen of 100,000 compound library to Identify Inhibitors of Mycobacterium tuberculosis H37Rv | 100685 | 1594 | |
| antiBacterial | tuberculosis | Mycobacterium Tuberculosis | phenotypic | High throughput screen for small molecule inhibitors of a hypoxia-regulated fluorescent biosensor in Mycobacterium tuberculosis | 300060 | 312 | |
| metabolicEndocrine | obesity | LipidDropletFormation | phenotypic | High Throughput Imaging Assay for Hepatic Lipid Droplet Formation | 236434 | 954 | |
| biologicalProcess | dementia | betaCateninTranslocation | targetBased | High Throughput Imaging Assay for Beta-Catenin | CTNNB1 | 193542 | 587 |
| urinarySystem | renal tubular transport disease | KCNJ1 | targetBased | High throughput discovery of novel modulators of ROMK K+ channel activity: Primary Screen | KCNJ1 | 125268 | 2463 |
| PTBP1 | targetBased | High Content Assay for Compounds that inhibit the Assembly of the Perinucleolar Compartment | PTBP1 | 139718 | 4338 | ||
| biologicalProcess | stressResponse | HSF1_activators | targetBased | Heat Shock Factor-1 (HSF-1) Measured in Cell-Based System Using Plate Reader - 2038-01_Activator_SinglePoint_HTS_Activity | HSF1 | 301170 | 5173 |
| biologicalProcess | proteinTransport | DyneinTransport | phenotypic | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. | 219902 | 1036 | |
| metabolicEndocrine | insulinSignaling | InsulinPromoterDownRegulation | phenotypic | HCS for Compounds that Up-Regulate Insulin Promoter Activity in MIN6 Cells | 192980 | 574 | |
| metabolicEndocrine | insulinSignaling | InsulinPromoterDownRegulation | phenotypic | HCS for Compounds that Down-Regulate Insulin Promoter Activity in MIN6 Cells | 192372 | 925 | |
| dermatology | skin disease | TUBB | targetBased | HCS assay for microtubule stabilizers | TUBB | 195821 | 1625 |
| visualSystem | eye disease | GBA1 | targetBased | Glucocerebrosidase | GBA1 | 48118 | 549 |
| metabolicEndocrine | systolic blood pressure | RAD52 | targetBased | FRET-based HTS for detection of RAD52 Inhibitors Measured in Biochemical System Using Plate Reader - 7018-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | RAD52 | 352074 | 1608 |
| metabolicEndocrine | Energy balance, obesity | HCRTR1 | targetBased | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | 326024 | 5748 |
| antiBacterial | P. aeruginosa | Pseudomonas aeruginosa | targetBased | Fluorescent Biochemical Primary HTS to Identify Inhibitors of P. aeruginosa PvdQ acylase Measured in Biochemical System Using Plate Reader and Imaging Combination - 2091-01_Inhibitor_SinglePoint_HTS_Activity | PvdQ | 337500 | 213 |
| antiMicrobial | malaria | Plasmodium falciparum | targetBased | Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL). | Pf-apPOL | 201181 | 519 |
| otherPhenotypes | age at menarche | NPBWR1 | targetBased | Fluorescence-based primary cell-based high throughput screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7). | NPBWR1 | 290726 | 3127 |
| psychiatricDisorder | mental or behavioural disorder | OXTR | targetBased | Fluorescence-based primary cell-based high throughput screening assay to identify agonists of the Oxytocin Receptor (OXTR). | OXTR | 324747 | 1043 |
| antiViral | HCV | Hepacivirus hominis | targetBased | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) | NS3 | 290726 | 1635 |
| PPP5C | targetBased | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of Protein Phosphatase 5 (PP5). | PPP5C | 314999 | 564 | ||
| biologicalProcess | endocannabinoidSignaling | DAGLB_inhibitors | targetBased | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of human diacylglycerol lipase, beta (DAGLB) | DAGLB | 343468 | 202 |
| antiViral | HCV | Hepacivirus hominis | targetBased | Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors: biochemical high-throughput screening assay to identify compounds that cause fluorescent intercalator displacement (FID) | NS3 | 290725 | 487 |
| nervousSystem | neurodegeneration | CHRM1_PAMs | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1 | 359207 | 316 |
| biologicalProcess | M4_AcChBiology | CHRM5 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | 363803 | 1081 |
| nervousSystem | AD | CHRM4_PAMs | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4 | 363803 | 1450 |
| muculoEskeletalConnective | connective tissue disease | TLR9 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | TLR9 | 343468 | 734 |
| reproductiveSystem | male reproductive system disease | RIPK2 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and the receptor-interacting serine-threonine kinase 2 (RIPK2) | RIPK2 | 363803 | 1383 |
| psychiatricDisorder | insomnia | HCRTR1 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | HCRTR1 | 326024 | 1387 |
| nervousSystem | PD | TAAR1 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | 362577 | 5374 |
| respiratory | respiratoryDisorders | CHRM1_antgonists | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1 | 359207 | 4555 |
| biologicalProcess | M4_AcChBiology | CHRM5 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | 363803 | 2133 |
| nervousSystem | PD | CHRM4_antgonists | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4 | 363803 | 2629 |
| psychiatricDisorder | anxiety | GALR3_antagonists | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) | GALR3 | 357859 | 1562 |
| psychiatricDisorder | schizophrenia | TAAR1 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) | TAAR1 | 362577 | 3573 |
| biologicalProcess | M4_AcChBiology | CHRM5 | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | 363803 | 698 |
| nervousSystem | psychosis | CHRM4_agonists | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4 | 363803 | 502 |
| nervousSystem | neurodegeneration | CHRM1_agonists | targetBased | Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1 | 359207 | 1189 |
| nervousSystem | huntington | cagRnaRepeats | phenotypic | Fluorescence-based biochemical primary high throughput screening assay to identify molecules that bind r(CAG) RNA repeats | 368927 | 4667 | |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | targetBased | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | FBA | 359207 | 8215 |
| muculoEskeletalConnective | hypertrophic cardiomyopathy | TNNI3 | targetBased | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | 335238 | 390 |
| muculoEskeletalConnective | hypertrophic cardiomyopathy | TNNI3 | targetBased | Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | 335239 | 801 |
| immune | autoimmuneDisorders | TCR-CD3 interaction | phenotypic | Fluorescence-based biochemical primary high throughput assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled TCR probe | 362574 | 1343 | |
| antiViral | CCHFV | Crimean-Congo Hemorrhagic Fever (CCHF) virus | targetBased | Fluorescence-based biochemical high throughput screening primary assay to identify inhibitors of Crimean-Congo Hemorrhagic Fever (CCHF) viral ovarian tumor domain protease (vOTU): Pep-AMC substrate | vOTU | 368927 | 2045 |
| antiMicrobial | trypanosomiasis | Trypanosoma brucei brucei | targetBased | Fluorescence-based biochemical high throughput primary assay to identify inhibitors of Trypanosoma brucei RNA editing ligase 1 (TbREL1) | REL1 | 89157 | 438 |
| biologicalProcess | toolCompoundsMultiDiseases | PLCG1 | targetBased | Fluorescence-based biochemical high throughput primary assay to identify inhibitors of phospholipase C isozymes (PLC-gamma1). | PLCG1 | 369953 | 3123 |
| geneticDisorder | spondylometaphyseal dysplasia with corneal dystrophy | PLCB3 | targetBased | Fluorescence-based biochemical high throughput primary assay to identify inhibitors of phospholipase C isozymes (PLC-beta3). | PLCB3 | 369953 | 662 |
| antiFungal | antifungal | TPT1 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). | TPT1 | 302663 | 2452 |
| metabolicEndocrine | inborn disorder of amino acid transport | PREPL | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) | PREPL | 324747 | 2221 |
| dermatology | skin disease | PLA2G7 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | PLA2G7 | 326024 | 4934 |
| psychiatricDisorder | cerebral arteriopathy with subcortical infarcts and leukoencephalopathy | HTRA1 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the HTRA serine peptidase 1 (HTRA1) | HTRA1 | 343467 | 1710 |
| antiViral | EBV | Epstein-Barr virus | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the Epstein-Barr virus nuclear antigen 1 (EBNA-1). | BKRF1 | 302663 | 1022 |
| nervousSystem | neurodegeneration | PPME1 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Phosphatase Methylesterase 1 (PME-1). | PPME1 | 314999 | 1683 |
| muculoEskeletalConnective | connective tissue disease | PADI4 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) (1536 HTS) | PADI4 | 326022 | 1334 |
| nervousSystem | neurodegeneration | MCL1 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. | MCL1 | 314998 | 2139 |
| psychiatricDisorder | pervasive developmental disorder | PAFAH1B3 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of human platelet-activating factor acetylhydrolase 1B, catalytic subunit 3 (PAFAH1B3) | PAFAH1B3 | 335239 | 928 |
| nervousSystem | neurodegeneration | PAFAH1B2 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of human platelet-activating factor acetylhydrolase 1b, catalytic subunit 2 (PAFAH1B2) | PAFAH1B2 | 335239 | 4158 |
| muculoEskeletalConnective | bone fracture related measurement | PAFAH2 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of human platelet activating factor acetylhydrolase 2 (PAFAH2) | PAFAH2 | 335239 | 3325 |
| GLD-1 | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of GLD-1 protein - TGE RNA interaction. | GLD-1 | 324746 | 1419 | ||
| antiBacterial | E. coli | Escherichia coli (strain K12) | targetBased | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Escherichia coli DNA-binding ATP-dependent protease La (eLon) | LON | 362020 | 1524 |
| geneticDisorder | genetic, familial or congenital disease | ABHD17B | targetBased | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. | ABHD17B | 302663 | 993 |
| nervousSystem | neurodegeneration | GSTO1 | targetBased | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). | GSTO1 | 302663 | 3200 |
| metabolicEndocrine | endocrine pancreas disorder | IDE | targetBased | Fluorescence polarization-based cell-based primary high throughput screening assay to identify inhibitors of insulin-degrading enzyme (IDE) | IDE | 324747 | 1316 |
| metabolicEndocrine | endocrine pancreas disorder | IDE | targetBased | Fluorescence polarization-based cell-based primary high throughput screening assay to identify activators of insulin-degrading enzyme (IDE) | IDE | 335239 | 245 |
| hematologic | coagulation protein disease | FGB_inhibitors | targetBased | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn7) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB | 369953 | 498 |
| hematologic | coagulation protein disease | FGB_inhibitors | targetBased | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn6) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB | 369953 | 760 |
| biologicalProcess | prospectiveBiology | ASAP1_inhibitors | targetBased | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1) | ASAP1 | 362577 | 680 |
| nervousSystem | AD | ARFGAP1_inhibitors | targetBased | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ADP-ribosylation factor GTPase activating protein 1 (ARFGAP1) | ARFGAP1 | 362539 | 954 |
| geneticDisorder | cardioacrofacial dysplasia 2 | PRKACB | targetBased | Fluorescence polarization-based biochemical primary high throughput screening assay to identify activators of the Protein Kinase A-R2B (PKA-R2B) complex | PRKACB | 343468 | 273 |
| cancer | neoplastic disease or syndrome | PRKAR1A | targetBased | Fluorescence polarization-based biochemical primary high throughput screening assay to identify activators of the Protein Kinase A-R1A (PKA-R1A) complex | PRKAR1A | 343468 | 285 |
| immune | autoimmune disease | SIAE | targetBased | Fluorescence polarization-based biochemical high throughput primary assay to identify inhibitors of sialic acid acetylesterase (SIAE) | SIAE | 369933 | 2555 |
| metabolicEndocrine | obesity | ABHD4_inhibitors | targetBased | Fluorescence polarization-based biochemical high throughput primary assay to identify inhibitors of alpha/beta hydrolase domain containing 4 (ABHD4). | ABHD4 | 369953 | 2005 |
| rareDiseases | cysticFibrosis | cftrTrafficModulators | targetBased | Fluorescence Polarization with CAL-PDZ Measured in Biochemical System Using Plate Reader - 2109-02_Inhibitor_SinglePoint_HTS_Activity | CFTR | 296501 | 2737 |
| cancer | neoplastic disease or syndrome | KEAP1 | targetBased | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity | KEAP1 | 336894 | 489 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis | targetBased | Fluorescence polarization to screen for inhibitor that competite the binding of FadD28 to bisubstrate Measured in Biochemical System Using Plate Reader - 2147-01_Inhibitor_SinglePoint_HTS_Activity | FadD28 | 355054 | 777 |
| antiViral | HHV-8 | Human herpesvirus 8 | targetBased | Fluorescence Polarization Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the LANA Histone H2A/H2B Interaction | LANA1 | 323564 | 1946 |
| immune | type II hypersensitivity reaction disease | PLK1 | targetBased | Fluorescence polarization assay for PLK1 inhibitors | PLK1 | 97099 | 518 |
| cancer | neoplastic disease or syndrome | KLK7 | targetBased | Fluorescence Intensity-based biochemical primary high throughput screening assay to identify activators of kallikrein-7 (K7) zymogen | KLK7 | 368927 | 3325 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | targetBased | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of RecA Intein Splicing Activity | RECA | 293376 | 2191 |
| cancer | neoplastic disease or syndrome | RCE1 | targetBased | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme | RCE1 | 294698 | 799 |
| biologicalProcess | cellDivision | RanGTP-Importin-beta complex inhibitors | phenotypic | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the RanGTP-Importin-beta complex | 302387 | 3282 | |
| cancer | neoplastic disease or syndrome | HDAC3 | targetBased | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of Histone Deacetylase 3 | HDAC3 | 318291 | 483 |
| antiFungal | candidiasis | fluconazole-resistant C.albicans | phenotypic | Fluorescence Cell-Based Primary HTS of C.albicans growth in the presence of Fluconazole and compound | HSP90 | 302451 | 1736 |
| cancer | cancerGeneral | rosLevels | phenotypic | Fluorescence Cell-Based Primary HTS to Identify Reactive Oxygen Species Inducers in Cancer Cells Measured in Cell-Based System Using Plate Reader and Imaging Combination - 2044-01_Activator_SinglePoint_HTS_Activity | 45939 | 901 | |
| otherPhenotypes | age at menarche | KDM4C | targetBased | Fluorescence Biochemical Primary HTS to Identify Inhibitors of GASC-1 Activity | KDM4C | 326066 | 228 |
| immune | immunomodulation | CTL granule exocytosis | phenotypic | Flow Cytometric HTS Screening for Inhibitors of Lytic Granule Exocytosis with MLPCN Compound Library | 363875 | 2400 | |
| biologicalProcess | drugTransport | ABCB6_inhibitors | targetBased | Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for MLPCN Compound Set | ABCB6 | 362098 | 692 |
| cardioVascular | antithrombotic | F12_modulation | targetBased | Factor XIIa 1536 HTS | F12 | 217430 | 649 |
| cardioVascular | antithrombotic | F11_modulation | targetBased | Factor XIa 1536 HTS | F11 | 218707 | 302 |
| cancer | cancerGeneral | EZH2_inhibitors | targetBased | EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Reader - 2125-01_Inhibitor_SinglePoint_HTS_Activity | EZH2 | 57013 | 201 |
| antiBacterial | P. aeruginosa | Pseudomonas aeruginosa | targetBased | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase | BLAIMP-1 | 290726 | 1322 |
| nervousSystem | inherited neurodegenerative disorder | TDP2 | targetBased | Epi Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of human tyrosyl-DNA phosphodiesterase 2 (TDP2) | TDP2 | 369953 | 1241 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis, non-replicating, drug-tolerant | phenotypic | Elucidation of physiology of non-replicating, drug-tolerant Mycobacterium tuberculosis | 324433 | 1277 | |
| cancer | neoplastic disease or syndrome | MDM2 | targetBased | E3 Ligase HTS_1536 | MDM2 | 207811 | 220 |
| nervousSystem | geneticNeurodevelopmentalDisability | DYRK1A_inhibitors | targetBased | Dyrk1 A HTS Measured in Biochemical System Using Plate Reader - 2124-01_Inhibitor_SinglePoint_HTS_Activity | DYRK1A | 310014 | 1321 |
| antiViral | HCMV | Human cytomegalovirus | targetBased | Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress | NEC2 | 183911 | 278 |
| antiViral | H1N1 | Influenza A virus | targetBased | Discovery of Small Molecule Probes for H1N1 Influenza NS1A | NS1 | 335224 | 1010 |
| hematologic | normocytic anemia | RACGAP1 | targetBased | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Primary and Confirmatory Screens | RACGAP1 | 342059 | 2057 |
| respiratory | respiratoryDisorders | CHRM1_allosteric_antagonists | targetBased | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1 | 63656 | 2179 |
| nervousSystem | neurodegeneration | CHRM1_allosteric_activators | targetBased | Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1 | 63676 | 1938 |
| cancer | cancerGeneral | Dicer_inhibitors | targetBased | Dicer-mediated maturation of pre-microRNA | DICER1 | 46715 | 2829 |
| cancer | neoplastic disease or syndrome | NSD2 | targetBased | Development of Small Molecule Probes of the Histone Methyltransferase, NSD2 Measured in Biochemical System Using Plate Reader - 7053-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | NSD2 | 309684 | 1662 |
| antiViral | Dengue | dengueVirus | phenotypic | DENV2 CPE-Based HTS Measured in Cell-Based and Microorganism Combination System Using Plate Reader - 2149-01_Other_SinglePoint_HTS_Activity | 343305 | 5946 | |
| notSpecified | notSpecified | CYP2C19_inhibitors | targetBased | CYP2C19 Assay | CYP2C19 | 95857 | 20295 |
| notSpecified | notSpecified | CYP2C9_inhibitors | targetBased | CYP2C9 Assay | CYP2C9 | 95858 | 18730 |
| antiBacterial | E. coli | Escherichia coli O157:H7 | targetBased | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin | STX1 | 295619 | 37013 |
| cancer | neoplastic disease or syndrome | LYPLA1 | targetBased | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 1 (LYPLA1). | LYPLA1 | 314999 | 499 |
| nervousSystem | behavioralDisorders | AVPR1A_agonists | targetBased | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A | 324747 | 813 |
| psychiatricDisorder | schizophrenia | HTR5A | targetBased | Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | 335239 | 279 |
| nervousSystem | neurodegeneration | PPP1CA | targetBased | Counterscreen for inhibitors of PP5: fluorescence-based biochemical high throughput primary assay to identify inhibitors of Protein Phosphatase 1 (PP1). | PPP1CA | 314999 | 2841 |
| antiViral | EBV | Epstein-Barr virus | targetBased | Counterscreen for inhibitors of EBNA-1: fluorescence polarization-based biochemical high throughput primary assay to identify inhibitors of the Epstein-Barr virus-encoded protein, ZTA. | P03206 | 314999 | 485 |
| antiBacterial | H. pylori | Helicobacter pylori | phenotypic | Counterscreen for inhibitors of AddAB: absorbance-based bacterial cell-based high throughput screening assay to identify inhibitors of bacterial viability | 326024 | 893 | |
| nervousSystem | neurodegeneration | UHRF1 | targetBased | Counterscreen for inhibitors of 5-meCpG-binding domain protein 2 (MBD2): TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of binding of ubiquitin-like with PHD and ring finger domains 1 (UHRF1) to methylated oligonucleotide | UHRF1 | 369953 | 2779 |
| psychiatricDisorder | schizophrenia | HTR5A | targetBased | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | HTR5A | 335239 | 2035 |
| antiBacterial | Leuconostoc mesenteroides | Leuconostoc mesenteroides | targetBased | Counter Screen for Glucose-6-Phosphate Dehydrogenase-based Primary Assay | ZWF | 195560 | 236 |
| visualSystem | eye disease | NLRP1 | targetBased | Colorimetric Assay for Inhibitors for NALP1 | NLRP1 | 280024 | 1717 |
| antiBacterial | cholera | Vibrio cholerae BH1578 strain | phenotypic | Cholera Quorum: HTS for inducers of light production in the absence ofautoinducers using BH1578 (luxS deficient, cqsA deficient) Measured in Microorganism System Using Plate Reader - 2132-01_Agonist_SinglePoint_HTS_Activity | 349947 | 553 | |
| biologicalProcess | mitochondrialFusion | mitochondrialFusion | phenotypic | Chemical Genetic Screen to Identify Inhibitors of Mitochondrial Fusion - Primary Screen | 194153 | 4011 | |
| metabolicEndocrine | body fat percentage | GPR151 | targetBased | Cell-based high throughput primary assay to identify activators of GPR151 | GPR151 | 642701 | 6746 |
| geneticDisorder | chromosomal disorder | PMP22 | targetBased | Cell-based coincidence reporter assay to measure PMP22 gene transcription in S16 Pmp22-F2sN cells - Primary screen | PMP22 | 42576 | 834 |
| nervousSystem | longTermMemory | _modulators | targetBased | Cell signaling CRE-BLA (Fsk stim) | CREB | 69669 | 1744 |
| biologicalProcess | cytotoxicity | cytotox | phenotypic | cell growth assays at ChEMBL | |||
| antiMicrobial | malaria | Plasmodium falciparum | phenotypic | Calibr Malaria Delayed Death Assay SOP | 37708 | 433 | |
| antiBacterial | C. difficile | TcdB glycohydrolaseInhibitors | targetBased | C. difficile toxins: HTS for inhibitors of TcdB glycohydrolase activity Measured in Biochemical System Using Plate Reader - 7074-01_Inhibitor_SinglePoint_HTS_Activity | ToxB | 349124 | 837 |
| antiViral | HHV-8 | Human herpesvirus 8 | targetBased | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_SinglePoint_HTS_Activity | ORF73 | 336515 | 262 |
| antiArthropodal | hyphantria cunea | hyphantria cunea | targetBased | Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition | LGR2 | 375648 | 1337 |
| nervousSystem | PD | D2_PAMs | targetBased | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | DRD2 | 357537 | 806 |
| nervousSystem | psychosis | D2_antagonists | targetBased | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | DRD2 | 362274 | 1056 |
| nervousSystem | PD | D2_agonists | targetBased | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | DRD2 | 359518 | 300 |
| cancer | breastCancer | BrCaAvg | phenotypic | avg of cell line screens at ChEMBL | |||
| cancer | cancerGeneral | ARRB1_inhibitors | targetBased | Assay for Inhibitors of the beta-Arrestin-Adaptor Protein 2 Interaction That Mediate GPCR Degradation and Recycling | ARRB1 | 338373 | 1061 |
| psychiatricDisorder | mental or behavioural disorder | GRM8 | targetBased | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | GRM8 | 105151 | 2166 |
| cancer | neoplastic disease or syndrome | TACC3 | targetBased | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_SinglePoint_HTS_Activity | TACC3 | 391179 | 2589 |
| antiViral | BTV | Bluetongue virus (BTV) | phenotypic | Anti-Viral Drugs Against Arbovirus Infections, a Primary Screen | 195407 | 715 | |
| antiMicrobial | malaria | Plasmodium falciparum (isolate 3D7) | targetBased | Anti-Malarial Hsp90 Inhibitors Measured in Microorganism System Using Plate Reader - 2121-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | 811999 | 307132 | 972 |
| metabolicEndocrine | thyroid disease | TSHR | targetBased | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | TSHR | 329153 | 670 |
| nervousSystem | psychosis | D1_inhibitors | targetBased | Antagonist of Human D 1 Dopamine Receptor: qHTS | DRD1 | 355805 | 11440 |
| cancer | cancerGeneral | Pyk2 | targetBased | Antagonist identification of Pyk2 oligomerization: high-throughput screening cellular assay | PTK2B | 98749 | 818 |
| cancer | cancerGeneral | ULK1 | targetBased | AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of Unc-51 Like Autophagy Activating Kinase 1 (ULK1). | ULK1 | 30185 | 575 |
| cancer | melanoma | MITF inhibitors | targetBased | AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of microphthalmia-associated transcription factor (MITF) | MITF | 642362 | 5830 |
| cancer | cancerGeneral | E3 ligase activators | targetBased | AlphaScreen-based biochemical high throughput primary assay to identify activators of the E3 ligase (FBW7). | FBW7 | 641445 | 853 |
| nervousSystem | Huntington disease | HTT | targetBased | Alphascreen assay for small molecules abrogating mHTT-CaM Interaction | HTT | 189882 | 6790 |
| nervousSystem | PD | D1 | targetBased | Allosteric Modulators of D1 Receptors: Primary Screen | DRD1 | 57705 | 3413 |
| nervousSystem | PD | D1_activators | targetBased | Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | DRD1 | 361330 | 3713 |
| geneticDisorder | developmental defect during embryogenesis | MTOR | pathwayBased | Acumen qHTS Assay for Inhibitors of the mTORC1 Signaling Pathway in MEF (Tsc2-/-, p53-/-) Cells: Sytravon | MTOR | 43989 | 342 |
| nervousSystem | neurodegeneration | FOSB | targetBased | Activator for delta FosB/delta FosB homodimer Measured in Biochemical System Using Plate Reader - 2072-01_Activator_SinglePoint_HTS_Activity | FOSB | 337391 | 3330 |
| biologicalProcess | apoptosis | procaspase3Activators | targetBased | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 | CASP3 | 326024 | 350 |
| antiBacterial | E. coli | Escherichia coli (strain K12) | targetBased | Absorbance-based primary bacterial cell-based high throughput screening assay to identify inhibitors of RecBCD (with phage) | RECD | 362577 | 949 |
| antiBacterial | H. pylori | Helicobacter pylori | targetBased | Absorbance-based primary bacterial cell-based high throughput screening assay to identify inhibitors of AddAB recombination protein complex | AddAB | 326024 | 935 |
| MSRA | targetBased | Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) | MSRA | 362577 | 2709 | ||
| immune | fibrosis | MSRA | targetBased | Absorbance-based biochemical primary high throughput screening assay to identify activators of Methionine sulfoxide reductase A (MsrA) | MSRA | 362026 | 1074 |
| biologicalProcess | aging | superoxideGenerationInhibitors | phenotypic | A yeast HTS for caloric restriction mimetics that inhibit age-related superoxide | 328830 | 590 | |
| antiBacterial | salmonellosis | Salmonella Typhi | targetBased | A small molecule screen for inhibitors of the PhoP regulon in Salmonella Typhimurium | PhoB/PhoR | 300458 | 474 |
| antiBacterial | salmonellosis | Salmonella Typhimurium | targetBased | A small molecule screen for inhibitors of the PhoP regulon in Salmonella typhi | PhoB/PhoR | 305999 | 1018 |
| nervousSystem | neurodegeneration | UCHL5 | targetBased | A screen for small molecule inhibitors of the human deubiquitinating enzyme, UCH37 | UCHL5 | 330707 | 1075 |
| antiViral | Poliovirus type 1 | Poliovirus type 1 | targetBased | A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities | P03300 | 151525 | 1001 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | targetBased | A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis | MENB | 102628 | 440 |
| antiBacterial | anthrax | Bacillus anthracis | targetBased | A screen for compounds that inhibit the CapD enzyme of Bacillus anthracis | CapD | 138854 | 320 |
| antiBacterial | tuberculosis | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | targetBased | A screen for compounds that inhibit the bacterial siderophore biosynthetic enzyme MbtI | MBTI | 104192 | 927 |
| antiBacterial | S. aureus | Staphylococcus aureus | targetBased | A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus | LtaS | 168223 | 878 |
| antiBacterial | cholera | Vibrio cholerae serotype O1 | phenotypic | A screen for compounds that inhibit replication of Vibrio cholerae chromosome II | AAF95916 | 132441 | 351 |
| antiViral | VACV | Vaccinia virus (VACV) | targetBased | A screen for compounds that inhibit processive DNA synthesis of vaccinia virus | OPG071 | 45651 | 427 |
| antiBacterial | E. coli | Escherichia coli | phenotypic | A screen for compounds that inhibit growth of Escherichia coli | 327980 | 699 | |
| antiBacterial | S. aureus | Staphylococcus aureus | phenotypic | A screen for compounds that inhibit cell wall-associated teichoic acid synthesis in Staphylococcus aureus | 51739 | 4434 | |
| antiBacterial | S. aureus | Staphylococcus aureus RN4220 | phenotypic | A screen for compounds that are lethal to S. aureus RN4220 with the processive glycosyltransferase UgtP deleted | 327980 | 1782 | |
| antiBacterial | S. aureus | Staphylococcus aureus RN4220 | phenotypic | A screen for compounds that are lethal to S. aureus RN4220 | 327980 | 1062 | |
| PARK2 | pathwayBased | A Quantitative High throughput Screen to Identify Chemical Modulators of PINK1 Expression | PARK2 | 406283 | 823 | ||
| muculoEskeletalConnective | bone disease | GMNN | targetBased | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. | GMNN | 342279 | 6233 |
| muculoEskeletalConnective | bone disease | GMNN | targetBased | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. | GMNN | 343234 | 9888 |
| antiBacterial | E. coli | Escherichia coli O157:H7 | targetBased | A qHTS for Small Molecule Inhibitors of Shiga Toxin | STX1 | 292805 | 26874 |
| antiViral | VEEV | Venezuelan equine encephalitis virus | phenotypic | A Cell-Based Confirmatory Screen for Compounds that Inhibit VEEV, TC-83 | 347901 | 453 | |
| antiViral | RSV | Respiratory syncytial virus | phenotypic | A Cell Based HTS Approach for the Discovery of New Inhibitors of Respiratory syncytial virus (RSV) | 313719 | 409 | |
| antiViral | HIV | HIV type 1 | targetBased | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC | Hck-Nef | 220222 | 1495 |
| antiBacterial | 11_bacterialStrains | antibacterial | phenotypic | 11 gram + & - bacterial strains at ChEMBL | |||
| cancer | lungCancer | LuCa cell lines | phenotypic | 11 cell line screens at ChEMBL | |||
| cancer | colonCancer | CoCa cell lines | phenotypic | 9 cell line screens at ChEMBL | |||
| cancer | breastCancer | BrCa cell lines | phenotypic | 8 cell line screens at ChEMBL |
OpenTargets DB provides comprehensive insights into the relationships between genes, diseases, and drugs by combining data from various sources, including genomics, transcriptomics, and clinical research. Each gene from PubChem target-based screens will have multiple scored associations to multiple diseases based on qualitative and quantitative information from mentioned data sources so that indications recorded in PubChem can be expanded to a wide range of indications in multiple therapeutic areas.






























