OpenTargets offers > 27k target-disease associations from PChem targets suitable for virtual screening based in OpenTargets scores for immune diseases. See here the best scored pairs.
Check best scored target-disease associations in table:
PubChemAssay | program | assayType | testedComopunds | activeCompounds | diseaseName | weightedScore | weightedEvidence |
---|---|---|---|---|---|---|---|
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | Crohn's disease | 0.66633861809884 | 35 |
ROC1-CUL1 CTD Inhibitor di-Ub FRET Primary HTS Screen | RBX1 | targetBased | 143816 | 859 | Crohn's disease | 0.369489609878927 | 8 |
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 | targetBased | 363803 | 1383 | Crohn's disease | 0.332442928560379 | 8 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | Crohn's disease | 0.332959636528519 | 7 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | Crohn's disease | 0.332959636528519 | 7 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | Crohn's disease | 0.614524204063885 | 20 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | Crohn's disease | 0.297910135217532 | 32 |
HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | targetBased | 326888 | 645 | Crohn's disease | 0.737705438254737 | 75 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | Crohn's disease | 0.340694061111576 | 7 |
qHTS for Inhibitors of Cell Surface uPA Generation | PLAU | targetBased | 325247 | 1021 | Crohn's disease | 0.379885398185413 | 20 |
Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 771 | Crohn's disease | 0.325348050422973 | 14 |
Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 569 | Crohn's disease | 0.325348050422973 | 14 |
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 | targetBased | 99314 | 335 | Crohn's disease | 0.606813177486441 | 22 |
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 | targetBased | 196176 | 782 | Crohn's disease | 0.606813177486441 | 22 |
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 | targetBased | 99314 | 390 | Crohn's disease | 0.606813177486441 | 22 |
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 | targetBased | 196177 | 811 | Crohn's disease | 0.606813177486441 | 22 |
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 | targetBased | 196176 | 670 | Crohn's disease | 0.606813177486441 | 22 |
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 | targetBased | 196177 | 519 | Crohn's disease | 0.606813177486441 | 22 |
uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) | p47phoxInhibitors | targetBased | 217454 | 1142 | Crohn's disease | 0.266249542498813 | 6 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | Crohn's disease | 0.51331093980131 | 8 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | Crohn's disease | 0.923073177649278 | 1414 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | Crohn's disease | 0.5018282116886 | 13 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | Crohn's disease | 0.5018282116886 | 13 |
Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | targetBased | 55710 | 315 | Crohn's disease | 0.424333797212919 | 22 |
Primary Cell-based High Throughput Screening assay for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 979 | atopic eczema | 0.295300014382582 | 7 |
Primary Cell-based High Throughput Screening assay for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 278 | atopic eczema | 0.295300014382582 | 7 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | atopic eczema | 0.623231800016832 | 67 |
Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | AHR_activators | targetBased | 324747 | 7988 | atopic eczema | 0.410445598825414 | 13 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | atopic eczema | 0.417866746569554 | 23 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | targetBased | 316642 | 617 | atopic eczema | 0.316542135854887 | 11 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | atopic eczema | 0.439677534307829 | 6 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | targetBased | 86095 | 1442 | rheumatoid arthritis | 0.41826550590229 | 30 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | targetBased | 86095 | 1151 | rheumatoid arthritis | 0.41826550590229 | 30 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | rheumatoid arthritis | 0.68876863655042 | 227 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | rheumatoid arthritis | 0.408905740315506 | 8 |
uHTS identification of small molecule antagonists of the CCR6 receptor via a luminescent beta-arrestin assay | CCR6_antagonists | targetBased | 340696 | 1654 | rheumatoid arthritis | 0.523283731423149 | 34 |
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 | targetBased | 99314 | 335 | rheumatoid arthritis | 0.316170628682077 | 16 |
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 | targetBased | 196176 | 782 | rheumatoid arthritis | 0.316170628682077 | 16 |
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 | targetBased | 99314 | 390 | rheumatoid arthritis | 0.316170628682077 | 16 |
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 | targetBased | 196177 | 811 | rheumatoid arthritis | 0.316170628682077 | 16 |
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 | targetBased | 196176 | 670 | rheumatoid arthritis | 0.316170628682077 | 16 |
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 | targetBased | 196177 | 519 | rheumatoid arthritis | 0.316170628682077 | 16 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) (1536 HTS) | PADI4 | targetBased | 326022 | 1334 | rheumatoid arthritis | 0.687131196796391 | 53 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | rheumatoid arthritis | 0.344497760009479 | 15 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | targetBased | 316642 | 617 | rheumatoid arthritis | 0.518622044684266 | 7 |
Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | TLR9 | targetBased | 343468 | 734 | rheumatoid arthritis | 0.666736202498445 | 133 |
HTS for developing T Cell Immune Modulators | ITGAL | targetBased | 326271 | 221 | psoriasis | 0.647172633973302 | 119 |
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 | targetBased | 336894 | 489 | psoriasis | 0.519072092168666 | 26 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | psoriasis | 0.52623853206338 | 110 |
Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | AHR_activators | targetBased | 324747 | 7988 | psoriasis | 0.687648482714935 | 222 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | psoriasis | 0.339337400587504 | 695 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | psoriasis | 0.339337400587504 | 695 |
qHTS of IL-2 Activators | IL2 | targetBased | 364617 | 238 | psoriasis | 0.321063444162615 | 207 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | psoriasis | 0.368222903581623 | 914 |
qHTS for Inhibitors of Cell Surface uPA Generation | PLAU | targetBased | 325247 | 1021 | psoriasis | 0.318702620448013 | 12 |
VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | RORC | targetBased | 304060 | 10600 | psoriasis | 0.276155592989189 | 65 |
qHTS assay to identify small molecule antagonists of the retinoid-related orphan receptor gamma (ROR-gamma) signaling pathway | RORCgammaPathwayInhibitors | pathwayBased | 7671 | 874 | psoriasis | 0.276155592989189 | 65 |
qHTS for inhibitors of ROR gamma transcriptional activity | RORCgammaPathwayInhibitors | pathwayBased | 305439 | 16717 | psoriasis | 0.276155592989189 | 65 |
MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity | ERAP1_inhibitors | targetBased | 335777 | 499 | psoriasis | 0.546229169969465 | 140 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | psoriasis | 0.437397772906933 | 14 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | psoriasis | 0.351463457960425 | 502 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | psoriasis | 0.351463457960425 | 502 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | psoriasis | 0.682247545111168 | 296 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | targetBased | 316642 | 617 | psoriasis | 0.413899156141244 | 47 |
HTS for developing T Cell Immune Modulators | ITGAL | targetBased | 326271 | 221 | ulcerative colitis | 0.261097385083632 | 9 |
uHTS Identification of Diaphorase Inhibitors and Chemcical Oxidizers: Counter Screen for Diaphorase-based Primary Assays | DiaphoraseInhibitors | targetBased | 194152 | 1342 | ulcerative colitis | 0.464712841053478 | 21 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | targetBased | 86095 | 1442 | ulcerative colitis | 0.324962882417437 | 192 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | targetBased | 86095 | 1151 | ulcerative colitis | 0.324962882417437 | 192 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | ulcerative colitis | 0.760994816046525 | 161 |
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 | targetBased | 363803 | 1383 | ulcerative colitis | 0.299642360244183 | 21 |
EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Reader - 2125-01_Inhibitor_SinglePoint_HTS_Activity | EZH2_inhibitors | targetBased | 57013 | 201 | ulcerative colitis | 0.315719626583571 | 30 |
Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | AHR_activators | targetBased | 324747 | 7988 | ulcerative colitis | 0.33787439712456 | 74 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | ulcerative colitis | 0.328488655948732 | 68 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | ulcerative colitis | 0.446337451033987 | 696 |
HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | targetBased | 326888 | 645 | ulcerative colitis | 0.655877863539481 | 66 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) | NR5A2 | targetBased | 363803 | 458 | ulcerative colitis | 0.518921467802981 | 15 |
qHTS for Inhibitors of Cell Surface uPA Generation | PLAU | targetBased | 325247 | 1021 | ulcerative colitis | 0.257406185494847 | 30 |
Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 771 | ulcerative colitis | 0.590697841480425 | 26 |
Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 569 | ulcerative colitis | 0.590697841480425 | 26 |
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 | targetBased | 99314 | 335 | ulcerative colitis | 0.692888906416013 | 432 |
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 | targetBased | 196176 | 782 | ulcerative colitis | 0.692888906416013 | 432 |
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 | targetBased | 99314 | 390 | ulcerative colitis | 0.692888906416013 | 432 |
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 | targetBased | 196177 | 811 | ulcerative colitis | 0.692888906416013 | 432 |
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 | targetBased | 196176 | 670 | ulcerative colitis | 0.692888906416013 | 432 |
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 | targetBased | 196177 | 519 | ulcerative colitis | 0.692888906416013 | 432 |
qHTS assay for re-activators of p53 using a Luc reporter | TP53 | pathwayBased | 321427 | 201 | ulcerative colitis | 0.335150295135842 | 483 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54509 | 528 | ulcerative colitis | 0.335150295135842 | 483 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54513 | 338 | ulcerative colitis | 0.335150295135842 | 483 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 125394 | 1890 | ulcerative colitis | 0.335150295135842 | 483 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 124022 | 1156 | ulcerative colitis | 0.335150295135842 | 483 |
HTS Assay for Inhibitors of Akt Phophorylation: Primary Screen | AKT1_inhibitors | targetBased | 356517 | 1139 | ulcerative colitis | 0.328864540185122 | 323 |
VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | RORC | targetBased | 304060 | 10600 | ulcerative colitis | 0.385177046740896 | 41 |
qHTS assay to identify small molecule antagonists of the retinoid-related orphan receptor gamma (ROR-gamma) signaling pathway | RORCgammaPathwayInhibitors | pathwayBased | 7671 | 874 | ulcerative colitis | 0.385177046740896 | 41 |
qHTS for inhibitors of ROR gamma transcriptional activity | RORCgammaPathwayInhibitors | pathwayBased | 305439 | 16717 | ulcerative colitis | 0.385177046740896 | 41 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | ulcerative colitis | 0.30837818021927 | 33 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | ulcerative colitis | 0.477180480331524 | 32 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | ulcerative colitis | 0.802339118184399 | 318 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | ulcerative colitis | 0.359123268930043 | 351 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | ulcerative colitis | 0.359123268930043 | 351 |
OTUD3 deubiquitinase inhibition: Primary qHTS | OTUD3 | targetBased | 47480 | 334 | ulcerative colitis | 0.343824520808528 | 39 |
Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | targetBased | 55710 | 315 | ulcerative colitis | 0.644099885304213 | 123 |
Acumen qHTS Assay for Inhibitors of the mTORC1 Signaling Pathway in MEF (Tsc2-/-, p53-/-) Cells: Sytravon | MTOR | pathwayBased | 43989 | 342 | ulcerative colitis | 0.42005545401222 | 150 |
Primary qHTS for Inhibitors of ATXN expression | ATXN2_repressors | targetBased | 358434 | 2554 | celiac disease | 0.269403932902958 | 14 |
Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | TLR9 | targetBased | 343468 | 734 | ulcerative colitis | 0.354954988090465 | 61 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | ulcerative colitis | 0.494586180209997 | 950 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | ulcerative colitis | 0.494586180209997 | 950 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | colitis | 0.457463840244192 | 110 |
HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | targetBased | 326888 | 645 | colitis | 0.274984130748396 | 35 |
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 | targetBased | 99314 | 335 | colitis | 0.305284900636795 | 518 |
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 | targetBased | 196176 | 782 | colitis | 0.305284900636795 | 518 |
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 | targetBased | 99314 | 390 | colitis | 0.305284900636795 | 518 |
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 | targetBased | 196177 | 811 | colitis | 0.305284900636795 | 518 |
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 | targetBased | 196176 | 670 | colitis | 0.305284900636795 | 518 |
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 | targetBased | 196177 | 519 | colitis | 0.305284900636795 | 518 |
VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | RORC | targetBased | 304060 | 10600 | colitis | 0.29549917499103 | 62 |
qHTS assay to identify small molecule antagonists of the retinoid-related orphan receptor gamma (ROR-gamma) signaling pathway | RORCgammaPathwayInhibitors | pathwayBased | 7671 | 874 | colitis | 0.29549917499103 | 62 |
qHTS for inhibitors of ROR gamma transcriptional activity | RORCgammaPathwayInhibitors | pathwayBased | 305439 | 16717 | colitis | 0.29549917499103 | 62 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | colitis | 0.346136900375504 | 358 |
Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | TLR9 | targetBased | 343468 | 734 | antiphospholipid syndrome | 0.317964370558289 | 6 |
qHTS assay for MDR1-selective chemotherapeutics: Primary screen using the drug-selected MDR subline cells KB-V1 | MDR1-selective compounds | targetBased | 396029 | 13426 | inflammatory bowel disease | 0.276235168570378 | 134 |
qHTS assay for MDR1-selective chemotherapeutics: Primary screen using the parental adenocarcinoma cell KB-3-1 | MDR1-selective compounds | targetBased | 395981 | 5516 | inflammatory bowel disease | 0.276235168570378 | 134 |
uHTS Identification of Diaphorase Inhibitors and Chemcical Oxidizers: Counter Screen for Diaphorase-based Primary Assays | DiaphoraseInhibitors | targetBased | 194152 | 1342 | inflammatory bowel disease | 0.442884054302183 | 14 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | inflammatory bowel disease | 0.577230617368294 | 191 |
qHTS for Inhibitors of TGF-b | TGFB1 | pathwayBased | 403345 | 4970 | inflammatory bowel disease | 0.255444106574039 | 1009 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | inflammatory bowel disease | 0.47424467902973 | 338 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | inflammatory bowel disease | 0.429537177851221 | 1828 |
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 | targetBased | 335239 | 991 | inflammatory bowel disease | 0.450159732473526 | 26 |
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 | targetBased | 335239 | 695 | inflammatory bowel disease | 0.450159732473526 | 26 |
HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | targetBased | 326888 | 645 | inflammatory bowel disease | 0.539973454347842 | 88 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | inflammatory bowel disease | 0.316933224547464 | 53 |
Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) | NR5A2 | targetBased | 363803 | 458 | inflammatory bowel disease | 0.429840930588652 | 33 |
Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 771 | inflammatory bowel disease | 0.263404934707527 | 29 |
Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 569 | inflammatory bowel disease | 0.263404934707527 | 29 |
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 | targetBased | 99314 | 335 | inflammatory bowel disease | 0.593795823724006 | 632 |
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 | targetBased | 196176 | 782 | inflammatory bowel disease | 0.593795823724006 | 632 |
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 | targetBased | 99314 | 390 | inflammatory bowel disease | 0.593795823724006 | 632 |
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 | targetBased | 196177 | 811 | inflammatory bowel disease | 0.593795823724006 | 632 |
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 | targetBased | 196176 | 670 | inflammatory bowel disease | 0.593795823724006 | 632 |
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 | targetBased | 196177 | 519 | inflammatory bowel disease | 0.593795823724006 | 632 |
VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | RORC | targetBased | 304060 | 10600 | inflammatory bowel disease | 0.401130853590169 | 81 |
qHTS assay to identify small molecule antagonists of the retinoid-related orphan receptor gamma (ROR-gamma) signaling pathway | RORCgammaPathwayInhibitors | pathwayBased | 7671 | 874 | inflammatory bowel disease | 0.401130853590169 | 81 |
qHTS for inhibitors of ROR gamma transcriptional activity | RORCgammaPathwayInhibitors | pathwayBased | 305439 | 16717 | inflammatory bowel disease | 0.401130853590169 | 81 |
QFRET-based biochemical primary high throughput screening assay to identify exosite inhibitors of ADAM17. | ADAM17_inhibitors | targetBased | 369953 | 3080 | inflammatory bowel disease | 0.274356875163875 | 282 |
uHTS Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase | ALPI_inhibitors | targetBased | 330392 | 393 | inflammatory bowel disease | 0.551025850997796 | 30 |
uHTS Luminescent assay for identification of inhibitors of mouse intestinal alkaline phosphatase | ALPI_inhibitors | targetBased | 331670 | 664 | inflammatory bowel disease | 0.551025850997796 | 30 |
Luminescent assay for identification of activators of bovine intestinal alkaline phosphatase | ALPI_activators | targetBased | 195570 | 326 | inflammatory bowel disease | 0.551025850997796 | 30 |
uHTS Luminescent assay for identification of activators of human intestinal alkaline phosphatase | ALPI_activators | targetBased | 330392 | 537 | inflammatory bowel disease | 0.551025850997796 | 30 |
uHTS Luminescent assay for identification of activators of mouse intestinal alkaline phosphatase | ALPI_activators | targetBased | 331670 | 785 | inflammatory bowel disease | 0.551025850997796 | 30 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | inflammatory bowel disease | 0.532992751133878 | 89 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | inflammatory bowel disease | 0.703692814590368 | 1872 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | inflammatory bowel disease | 0.426166728756354 | 892 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | inflammatory bowel disease | 0.426166728756354 | 892 |
OTUD3 deubiquitinase inhibition: Primary qHTS | OTUD3 | targetBased | 47480 | 334 | inflammatory bowel disease | 0.32166348562018 | 32 |
Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | targetBased | 55710 | 315 | inflammatory bowel disease | 0.28469229931646 | 111 |
qHTS for Inhibitors of Cell Surface uPA Generation | PLAU | targetBased | 325247 | 1021 | inflammatory bowel disease | 0.400162717303332 | 25 |
Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | targetBased | 55710 | 315 | chronic progressive multiple sclerosis | 0.538635520397193 | 20 |
Primary Cell-based High Throughput Screening assay for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 979 | seasonal allergic rhinitis | 0.448820053202874 | 8 |
Primary Cell-based High Throughput Screening assay for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 278 | seasonal allergic rhinitis | 0.448820053202874 | 8 |
qHTS of IL-2 Activators | IL2 | targetBased | 364617 | 238 | seasonal allergic rhinitis | 0.332747471857003 | 11 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | seasonal allergic rhinitis | 0.43297757656177 | 17 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | targetBased | 359207 | 1189 | seasonal allergic rhinitis | 0.620287278383327 | 14 |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | targetBased | 63676 | 1938 | seasonal allergic rhinitis | 0.620287278383327 | 14 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | targetBased | 359207 | 316 | seasonal allergic rhinitis | 0.620287278383327 | 14 |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | targetBased | 63656 | 2179 | seasonal allergic rhinitis | 0.620287278383327 | 14 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | targetBased | 359207 | 4555 | seasonal allergic rhinitis | 0.620287278383327 | 14 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | targetBased | 339297 | 1446 | seasonal allergic rhinitis | 0.581326863490048 | 9 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | Vitiligo | 0.417884831049486 | 32 |
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 | targetBased | 336894 | 489 | relapsing-remitting multiple sclerosis | 0.64736606261308 | 54 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | relapsing-remitting multiple sclerosis | 0.303701503622198 | 12 |
HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | targetBased | 326888 | 645 | relapsing-remitting multiple sclerosis | 0.64002439670588 | 53 |
Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 771 | relapsing-remitting multiple sclerosis | 0.64372552302434 | 48 |
Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 569 | relapsing-remitting multiple sclerosis | 0.64372552302434 | 48 |
Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | targetBased | 55710 | 315 | relapsing-remitting multiple sclerosis | 0.655930591244198 | 144 |
Primary HTS Assay for S1P3 Antagonists | S1PR3 | targetBased | 169141 | 462 | relapsing-remitting multiple sclerosis | 0.643752814149123 | 48 |
Primary Cell-Based High-Throughput Screening to Identify Agonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | S1PR2 | targetBased | 96879 | 447 | relapsing-remitting multiple sclerosis | 0.643347103603292 | 47 |
Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | S1PR2 | targetBased | 96879 | 207 | relapsing-remitting multiple sclerosis | 0.643347103603292 | 47 |
Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 | procaspase3Activators | targetBased | 326024 | 350 | mucocutaneous lymph node syndrome | 0.495035722399972 | 65 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | acute graft vs. host disease | 0.515680643226986 | 9 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | targetBased | 305610 | 3878 | Myasthenia gravis | 0.628049159950515 | 18 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | targetBased | 305610 | 1082 | Myasthenia gravis | 0.628049159950515 | 18 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | targetBased | 305610 | 1552 | Myasthenia gravis | 0.628049159950515 | 18 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | targetBased | 343666 | 1267 | Myasthenia gravis | 0.628049159950515 | 18 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | targetBased | 342084 | 3260 | Myasthenia gravis | 0.628049159950515 | 18 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels | KCNQ2 | targetBased | 305609 | 3405 | Myasthenia gravis | 0.628049159950515 | 18 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels | KCNQ2 | targetBased | 305600 | 1644 | Myasthenia gravis | 0.628049159950515 | 18 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | autoimmune disease | 0.284976181084817 | 328 |
Fluorescence polarization-based biochemical high throughput primary assay to identify inhibitors of sialic acid acetylesterase (SIAE) | SIAE | targetBased | 369933 | 2555 | autoimmune disease | 0.70498382256379 | 32 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | autoimmune disease | 0.26935989249464 | 558 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | autoimmune disease | 0.259092984642321 | 3018 |
HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | targetBased | 326888 | 645 | autoimmune disease | 0.33909468052582 | 139 |
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 | targetBased | 99314 | 335 | autoimmune disease | 0.461685404329151 | 534 |
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 | targetBased | 196176 | 782 | autoimmune disease | 0.461685404329151 | 534 |
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 | targetBased | 99314 | 390 | autoimmune disease | 0.461685404329151 | 534 |
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 | targetBased | 196177 | 811 | autoimmune disease | 0.461685404329151 | 534 |
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 | targetBased | 196176 | 670 | autoimmune disease | 0.461685404329151 | 534 |
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 | targetBased | 196177 | 519 | autoimmune disease | 0.461685404329151 | 534 |
QFRET-based biochemical primary high throughput screening assay to identify exosite inhibitors of ADAM17. | ADAM17_inhibitors | targetBased | 369953 | 3080 | autoimmune disease | 0.267975631196369 | 285 |
uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) | p47phoxInhibitors | targetBased | 217454 | 1142 | autoimmune disease | 0.313808795263764 | 79 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) (1536 HTS) | PADI4 | targetBased | 326022 | 1334 | autoimmune disease | 0.424809734170857 | 159 |
Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | TSHR | targetBased | 329153 | 670 | autoimmune disease | 0.270604544732409 | 1003 |
Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | TSHR | targetBased | 329153 | 670 | autoimmune disease | 0.270604544732409 | 1003 |
qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor | TSHR | targetBased | 72026 | 352 | autoimmune disease | 0.270604544732409 | 1003 |
qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | TSHR | targetBased | 72026 | 1794 | autoimmune disease | 0.270604544732409 | 1003 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | autoimmune disease | 0.427740335161443 | 100 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | autoimmune disease | 0.322850001488186 | 1212 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | autoimmune disease | 0.897704362357904 | 1295 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | autoimmune disease | 0.897704362357904 | 1295 |
Primary screen for compounds that activate Insulin promoter activity in TRM-6 cells | INS | targetBased | 128695 | 1039 | autoimmune disease | 0.568589520918476 | 192 |
Primary screen for compounds that inhibit Insulin promoter activity in TRM-6 cells | INS | targetBased | 127961 | 1153 | autoimmune disease | 0.568589520918476 | 192 |
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 | targetBased | 99314 | 335 | proctitis | 0.583175100421059 | 9 |
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 | targetBased | 196176 | 782 | proctitis | 0.583175100421059 | 9 |
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 | targetBased | 99314 | 390 | proctitis | 0.583175100421059 | 9 |
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 | targetBased | 196177 | 811 | proctitis | 0.583175100421059 | 9 |
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 | targetBased | 196176 | 670 | proctitis | 0.583175100421059 | 9 |
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 | targetBased | 196177 | 519 | proctitis | 0.583175100421059 | 9 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | small bowel Crohn's disease | 0.286105916237584 | 14 |
Primary Cell-based High Throughput Screening assay for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 979 | allergic rhinitis | 0.485483319847018 | 22 |
Primary Cell-based High Throughput Screening assay for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 278 | allergic rhinitis | 0.485483319847018 | 22 |
Primary cell-based high throughput screening assay to identify inhibitors of kruppel-like factor 5 (KLF5) | KLF5 | targetBased | 290726 | 671 | allergic rhinitis | 0.332353881234872 | 7 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | allergic rhinitis | 0.447576648851219 | 199 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | allergic rhinitis | 0.447576648851219 | 199 |
qHTS of IL-2 Activators | IL2 | targetBased | 364617 | 238 | allergic rhinitis | 0.320282297274405 | 152 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | allergic rhinitis | 0.535980475306307 | 47 |
qHTS for Inhibitors of Inflammasome Signaling: IL-1-beta AlphaLISA Primary Screen | IL-1b Inflammasome | pathwayBased | 362051 | 17187 | allergic rhinitis | 0.386445309864048 | 181 |
VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | RORC | targetBased | 304060 | 10600 | allergic rhinitis | 0.30110251368226 | 17 |
qHTS assay to identify small molecule antagonists of the retinoid-related orphan receptor gamma (ROR-gamma) signaling pathway | RORCgammaPathwayInhibitors | pathwayBased | 7671 | 874 | allergic rhinitis | 0.30110251368226 | 17 |
qHTS for inhibitors of ROR gamma transcriptional activity | RORCgammaPathwayInhibitors | pathwayBased | 305439 | 16717 | allergic rhinitis | 0.30110251368226 | 17 |
qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | ALOX15_inhibitors | targetBased | 73174 | 1034 | allergic rhinitis | 0.411026948368507 | 11 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | allergic rhinitis | 0.532859659476675 | 20 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | targetBased | 359207 | 1189 | allergic rhinitis | 0.627077400922343 | 17 |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | targetBased | 63676 | 1938 | allergic rhinitis | 0.627077400922343 | 17 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | targetBased | 359207 | 316 | allergic rhinitis | 0.627077400922343 | 17 |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | targetBased | 63656 | 2179 | allergic rhinitis | 0.627077400922343 | 17 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | targetBased | 359207 | 4555 | allergic rhinitis | 0.627077400922343 | 17 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | targetBased | 339297 | 1446 | allergic rhinitis | 0.548658639799238 | 14 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | targetBased | 316642 | 617 | allergic rhinitis | 0.427563036899599 | 34 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | targetBased | 316642 | 617 | lupus nephritis | 0.368678188787264 | 6 |
qHTS assay for re-activators of p53 using a Luc reporter | TP53 | pathwayBased | 321427 | 201 | lymphatic system disease | 0.293285626205835 | 1400 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54509 | 528 | lymphatic system disease | 0.293285626205835 | 1400 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54513 | 338 | lymphatic system disease | 0.293285626205835 | 1400 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 125394 | 1890 | lymphatic system disease | 0.293285626205835 | 1400 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 124022 | 1156 | lymphatic system disease | 0.293285626205835 | 1400 |
Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | BCL2L11_inhibitors | targetBased | 325630 | 216 | lymphatic system disease | 0.277557010338014 | 91 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | interleukin 1 receptor-like 1 measurement | 0.516816961193787 | 14 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | interleukin 18 receptor 1 measurement | 0.346397165145154 | 11 |
Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | targetBased | 55710 | 315 | secondary progressive multiple sclerosis | 0.487644718997637 | 42 |
Cell-based coincidence reporter assay to measure PMP22 gene transcription in S16 Pmp22-F2sN cells - Primary screen | PMP22 | targetBased | 42576 | 834 | chronic inflammatory demyelinating polyneuropathy | 0.634841225279261 | 45 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | STAT3 gain of function | 0.606952560260641 | 770 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | STAT3 gain of function | 0.606952560260641 | 770 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | targetBased | 305610 | 1552 | neuroinflammatory disorder | 0.428791740822698 | 18 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | targetBased | 343666 | 1267 | neuroinflammatory disorder | 0.428791740822698 | 18 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | targetBased | 342084 | 3260 | neuroinflammatory disorder | 0.428791740822698 | 18 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | pathwayBased | 70898 | 707 | neuroinflammatory disorder | 0.395913906802846 | 7 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | pathwayBased | 131324 | 544 | neuroinflammatory disorder | 0.395913906802846 | 7 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | neuroinflammatory disorder | 0.412009492152627 | 161 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | neuroinflammatory disorder | 0.412009492152627 | 161 |
qHTS for Inhibitors of TGF-b | TGFB1 | pathwayBased | 403345 | 4970 | inflammatory bowel disease, immunodeficiency, and encephalopathy | 0.752376428542243 | 30 |
Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation | WEE1 | targetBased | 217959 | 2616 | neuroinflammatory disorder | 0.424632003390909 | 9 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | neuroinflammatory disorder | 0.465852538787439 | 39 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | neuroinflammatory disorder | 0.465852538787439 | 39 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | targetBased | 339297 | 1446 | neuroinflammatory disorder | 0.303641809113339 | 7 |
TRFRET-based cell-based primary high throughput screening assay to identify inhibitors of cell surface Prion Protein (PRPC) | PRNP | targetBased | 369953 | 1596 | neuroinflammatory disorder | 0.362258189767571 | 7 |
Acumen qHTS Assay for Inhibitors of the mTORC1 Signaling Pathway in MEF (Tsc2-/-, p53-/-) Cells: Sytravon | MTOR | pathwayBased | 43989 | 342 | neuroinflammatory disorder | 0.450938815833541 | 24 |
qHTS for Inhibitors of Inflammasome Signaling: IL-1-beta AlphaLISA Primary Screen | IL-1b Inflammasome | pathwayBased | 362051 | 17187 | systemic inflammatory response syndrome | 0.297340349354546 | 203 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | macrophage activation syndrome | 0.307196122303397 | 131 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | psoriasis vulgaris | 0.655284149899379 | 86 |
Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | MC4R | targetBased | 356160 | 3470 | monogenic diabetes | 0.443040939126801 | 18 |
TRFRET-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): antagonists of MC4R | MC4R | targetBased | 356160 | 1703 | monogenic diabetes | 0.443040939126801 | 18 |
Primary screen for compounds that activate Insulin promoter activity in TRM-6 cells | INS | targetBased | 128695 | 1039 | monogenic diabetes | 0.723854062699688 | 131 |
Primary screen for compounds that inhibit Insulin promoter activity in TRM-6 cells | INS | targetBased | 127961 | 1153 | monogenic diabetes | 0.723854062699688 | 131 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | hypersensitivity reaction disease | 0.268730617640425 | 213 |
uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | targetBased | 330392 | 1295 | Inflammatory abnormality of the skin | 0.296789047816734 | 55 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | Immunodeficiency | 0.374658619756015 | 36 |
qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | BLM_inhibitors | targetBased | 347933 | 673 | Immunodeficiency | 0.507538257966889 | 8 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | Combined immunodeficiency | 0.509775695278464 | 11 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | Combined immunodeficiency | 0.509775695278464 | 11 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | Combined immunodeficiency | 0.509686858131481 | 33 |
qHTS for Suppressors of FUS Proteinopathy: Primary screen using FUS-linked yeast assay | FUS_asupressors | targetBased | 385746 | 932 | Amyotrophic lateral sclerosis | 0.411659407127753 | 675 |
qHTS of TDP-43 Inhibitors | TARDBP | pathwayBased | 403703 | 7150 | Amyotrophic lateral sclerosis | 0.42662742198745 | 2529 |
qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen | TARDBP | pathwayBased | 45163 | 203 | Amyotrophic lateral sclerosis | 0.42662742198745 | 2529 |
Primary biochemical high-throughput screening assay to measure P97 ATPase inhibition | VCP | targetBased | 217959 | 923 | Amyotrophic lateral sclerosis | 0.411250221903632 | 149 |
HCS assay for microtubule stabilizers | TUBB | targetBased | 195821 | 1625 | neutropenia | 0.429115894771016 | 18 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | hyper-IgM syndrome | 0.41140906059619 | 148 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | targetBased | 339297 | 1446 | allergic asthma | 0.305785418457101 | 20 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | inborn error of immunity | 0.567222711159724 | 483 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | inborn error of immunity | 0.567222711159724 | 483 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | inborn error of immunity | 0.260508250524808 | 558 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | inborn error of immunity | 0.35263597806567 | 286 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | inborn error of immunity | 0.323072945633956 | 978 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | inborn error of immunity | 0.323072945633956 | 978 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | inborn error of immunity | 0.321548150235644 | 156 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | inborn error of immunity | 0.309008733126974 | 490 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | inborn error of immunity | 0.309008733126974 | 490 |
Primary Cell-based High Throughput Screening assay for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 979 | allergic disease | 0.451288505056579 | 24 |
Primary Cell-based High Throughput Screening assay for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA) | RORA | pathwayBased | 64908 | 278 | allergic disease | 0.451288505056579 | 24 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | targetBased | 290355 | 265 | allergic disease | 0.511316437424948 | 6 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | allergic disease | 0.403052761694357 | 225 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | allergic disease | 0.403052761694357 | 225 |
qHTS of IL-2 Activators | IL2 | targetBased | 364617 | 238 | allergic disease | 0.343320178641678 | 170 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | allergic disease | 0.255964635028286 | 34 |
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 | targetBased | 335239 | 991 | allergic disease | 0.554877973171716 | 8 |
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 | targetBased | 335239 | 695 | allergic disease | 0.554877973171716 | 8 |
Small-molecule inhibitors of ST2 (IL1RL1) | IL1RL1 | targetBased | 75924 | 1804 | allergic disease | 0.518691103234877 | 71 |
qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | ALOX15_inhibitors | targetBased | 73174 | 1034 | allergic disease | 0.33358317257055 | 14 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | allergic disease | 0.540851322143723 | 28 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | targetBased | 339297 | 1446 | allergic disease | 0.628446114609922 | 34 |
HCS assay for microtubule stabilizers | TUBB | targetBased | 195821 | 1625 | allergic disease | 0.392468604405345 | 6 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | targetBased | 305610 | 3878 | multiple sclerosis | 0.645235750885557 | 44 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | targetBased | 305610 | 1082 | multiple sclerosis | 0.645235750885557 | 44 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | targetBased | 305610 | 1552 | multiple sclerosis | 0.645235750885557 | 44 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | targetBased | 343666 | 1267 | multiple sclerosis | 0.645235750885557 | 44 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | targetBased | 342084 | 3260 | multiple sclerosis | 0.645235750885557 | 44 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels | KCNQ2 | targetBased | 305609 | 3405 | multiple sclerosis | 0.645235750885557 | 44 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels | KCNQ2 | targetBased | 305600 | 1644 | multiple sclerosis | 0.645235750885557 | 44 |
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 | targetBased | 336894 | 489 | multiple sclerosis | 0.690530836424373 | 76 |
uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | OPRK1 | targetBased | 290355 | 265 | multiple sclerosis | 0.284952492325572 | 8 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | targetBased | 86095 | 1442 | multiple sclerosis | 0.304265510825839 | 41 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | targetBased | 86095 | 1151 | multiple sclerosis | 0.304265510825839 | 41 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | multiple sclerosis | 0.301837416904597 | 11 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | multiple sclerosis | 0.583926180418581 | 160 |
HTS for Identification of VLA-4 Allosteric Modulators from MLPCN library | ITGA4 | targetBased | 326888 | 645 | multiple sclerosis | 0.645671851693653 | 110 |
Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 771 | multiple sclerosis | 0.653518109271019 | 73 |
Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | S1PR4 | targetBased | 217959 | 569 | multiple sclerosis | 0.653518109271019 | 73 |
qHTS assay for re-activators of p53 using a Luc reporter | TP53 | pathwayBased | 321427 | 201 | multiple sclerosis | 0.511922137474039 | 26 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54509 | 528 | multiple sclerosis | 0.511922137474039 | 26 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54513 | 338 | multiple sclerosis | 0.511922137474039 | 26 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 125394 | 1890 | multiple sclerosis | 0.511922137474039 | 26 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 124022 | 1156 | multiple sclerosis | 0.511922137474039 | 26 |
HTS Assay for Inhibitors of Akt Phophorylation: Primary Screen | AKT1_inhibitors | targetBased | 356517 | 1139 | multiple sclerosis | 0.284450608994791 | 52 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | targetBased | 108286 | 1415 | multiple sclerosis | 0.602040251565065 | 19 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | multiple sclerosis | 0.330567104836404 | 30 |
Fluorescence polarization assay for PLK1 inhibitors | PLK1 | targetBased | 97099 | 518 | multiple sclerosis | 0.577168330395272 | 6 |
qHTS for Inhibitors of PLK1-PDB (polo-like kinase 1 - polo-box domain): Primary Screen | PLK1 | targetBased | 364065 | 10181 | multiple sclerosis | 0.577168330395272 | 6 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | multiple sclerosis | 0.464976182091521 | 78 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | multiple sclerosis | 0.464976182091521 | 78 |
Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | S1PR1 | targetBased | 55710 | 315 | multiple sclerosis | 0.664837114041353 | 511 |
S100A4: HTS Measured in Biochemical System Using Plate Reader - 7045-01_Inhibitor_SinglePoint_HTS_Activity | S100A4 | targetBased | 352235 | 501 | multiple sclerosis | 0.388943152731707 | 6 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | targetBased | 316642 | 617 | multiple sclerosis | 0.527972301614307 | 14 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | targetBased | 339772 | 8480 | multiple sclerosis | 0.554511094041346 | 18 |
Acumen qHTS Assay for Inhibitors of the mTORC1 Signaling Pathway in MEF (Tsc2-/-, p53-/-) Cells: Sytravon | MTOR | pathwayBased | 43989 | 342 | multiple sclerosis | 0.513718581157192 | 56 |
Primary HTS Assay for S1P3 Antagonists | S1PR3 | targetBased | 169141 | 462 | multiple sclerosis | 0.655299992173261 | 82 |
Primary Cell-Based High-Throughput Screening to Identify Agonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | S1PR2 | targetBased | 96879 | 447 | multiple sclerosis | 0.657352493094362 | 83 |
Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | S1PR2 | targetBased | 96879 | 207 | multiple sclerosis | 0.657352493094362 | 83 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | leukocyte adhesion deficiency 1 | 0.846366489681156 | 1155 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | hyper-IgE recurrent infection syndrome 1, autosomal dominant | 0.882249492479488 | 959 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | hyper-IgE recurrent infection syndrome 1, autosomal dominant | 0.882249492479488 | 959 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | immune deficiency disease | 0.316021335076101 | 957 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | immune deficiency disease | 0.316021335076101 | 957 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | Omenn syndrome | 0.773255884585553 | 42 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | hyper-IgM syndrome type 2 | 0.879623212791959 | 387 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | graft versus host disease | 0.624473599370751 | 132 |
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_interaction | targetBased | 359207 | 1432 | graft versus host disease | 0.329151702280302 | 47 |
uHTS identification of DNMT1 inhibitors in a Fluorescent Molecular Beacon assay | DNMT1 | targetBased | 359244 | 2975 | graft versus host disease | 0.289620981036984 | 8 |
Primary biochemical high-throughput screening assay for inhibitors of Rho kinase 2 (Rhok2) | ROCK2 | targetBased | 59788 | 212 | graft versus host disease | 0.530616370782023 | 24 |
Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | TLR9 | targetBased | 343468 | 734 | graft versus host disease | 0.287495758286774 | 32 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | combined immunodeficiency | 0.6056619781946 | 71 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | combined immunodeficiency | 0.6056619781946 | 71 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | combined immunodeficiency | 0.317197697603538 | 6424 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | combined immunodeficiency | 0.647259809976761 | 700 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome | 0.894516532057074 | 815 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome | 0.894516532057074 | 815 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | severe combined immunodeficiency | 0.700962625675913 | 816 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | agammaglobulinemia | 0.300066410503025 | 179 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | agammaglobulinemia | 0.300066410503025 | 179 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | chronic mucocutaneous candidiasis | 0.611677577432826 | 289 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | chronic mucocutaneous candidiasis | 0.611677577432826 | 289 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | hemophagocytic syndrome | 0.340446484450425 | 16 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | leukocyte adhesion deficiency | 0.750707304739755 | 536 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | hyper-IgE syndrome | 0.791517184926309 | 530 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | hyper-IgE syndrome | 0.791517184926309 | 530 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | T-B- severe combined immunodeficiency | 0.646206966714383 | 547 |
uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) | p47phoxInhibitors | targetBased | 217454 | 1142 | chronic granulomatous disease | 0.707233849788776 | 336 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | targetBased | 359518 | 300 | 22q11.2 deletion syndrome | 0.413346187350415 | 9 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | targetBased | 335652 | 1779 | 22q11.2 deletion syndrome | 0.413346187350415 | 9 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | targetBased | 362274 | 1056 | 22q11.2 deletion syndrome | 0.413346187350415 | 9 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | targetBased | 336308 | 6862 | 22q11.2 deletion syndrome | 0.413346187350415 | 9 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | targetBased | 357537 | 806 | 22q11.2 deletion syndrome | 0.413346187350415 | 9 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | targetBased | 339887 | 1178 | 22q11.2 deletion syndrome | 0.413346187350415 | 9 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | autoimmune enteropathy | 0.300697343647726 | 276 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | autoimmune enteropathy | 0.300697343647726 | 276 |
Primary biochemical high-throughput screening assay for inhibitors of Rho kinase 2 (Rhok2) | ROCK2 | targetBased | 59788 | 212 | chronic graft versus host disease | 0.327543716477058 | 35 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | immunodeficiency disease | 0.281553929492058 | 479 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | immunodeficiency disease | 0.281553929492058 | 479 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | immunodeficiency disease | 0.287801738691034 | 428 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | immunodeficiency disease | 0.287801738691034 | 428 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | immunodeficiency disease | 0.310321407554987 | 806 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | immunodeficiency disease | 0.315004903858155 | 857 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | immunodeficiency disease | 0.315004903858155 | 857 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | immunodeficiency 69 | 0.503413308689518 | 8 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | T-B+ severe combined immunodeficiency | 0.515494163057825 | 40 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | targetBased | 339297 | 1446 | anaphylaxis | 0.582453837228469 | 12 |
Nrf2 qHTS screen for inhibitors | nrf2Inhibitors | targetBased | 360873 | 7438 | immunodeficiency, developmental delay, and hypohomocysteinemia | 0.847171548352911 | 36 |
qHTS of Nrf2 Activators | Nrf2 activators | pathwayBased | 403871 | 1243 | immunodeficiency, developmental delay, and hypohomocysteinemia | 0.847171548352911 | 36 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | Chronic mucocutaneous candidosis | 0.898378085302774 | 825 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | Chronic mucocutaneous candidosis | 0.898378085302774 | 825 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | Autosomal dominant hyper-IgE syndrome | 0.882882834629081 | 1250 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | Autosomal dominant hyper-IgE syndrome | 0.882882834629081 | 1250 |
Toxoplasma gondii inhibition HTS in the presence of IFN-y | IFNG | targetBased | 67275 | 2509 | Primary hemophagocytic lymphohistiocytosis | 0.547474714183054 | 63 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | targetBased | 394050 | 3624 | inflammation | 0.286397190264778 | 13 |
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 | targetBased | 99314 | 335 | inflammation | 0.415910845994523 | 72 |
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 | targetBased | 196176 | 782 | inflammation | 0.415910845994523 | 72 |
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 | targetBased | 99314 | 390 | inflammation | 0.415910845994523 | 72 |
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 | targetBased | 196177 | 811 | inflammation | 0.415910845994523 | 72 |
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 | targetBased | 196176 | 670 | inflammation | 0.415910845994523 | 72 |
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 | targetBased | 196177 | 519 | inflammation | 0.415910845994523 | 72 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). | TPT1 | targetBased | 302663 | 2452 | Herpetic encephalitis | 0.28838130992472 | 6 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | Susceptibility to viral and mycobacterial infections | 0.849381507517208 | 756 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | Susceptibility to viral and mycobacterial infections | 0.849381507517208 | 756 |
uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | targetBased | 330392 | 1295 | Familial cold urticaria | 0.798662521910481 | 38 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | Leukocyte adhesion deficiency type I | 0.840099916485533 | 65 |
HTS of Smad transcription factor inhibitors | SMAD3 | targetBased | 88033 | 251 | Familial hemophagocytic lymphohistiocytosis | 0.392017533166542 | 8 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | type II hypersensitivity reaction disease | 0.267384674774844 | 170 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | type II hypersensitivity reaction disease | 0.302045298918466 | 408 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | type II hypersensitivity reaction disease | 0.302045298918466 | 408 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | type II hypersensitivity reaction disease | 0.314700577014956 | 687 |
Primary screen for compounds that activate Insulin promoter activity in TRM-6 cells | INS | targetBased | 128695 | 1039 | type II hypersensitivity reaction disease | 0.252318308693775 | 686 |
Primary screen for compounds that inhibit Insulin promoter activity in TRM-6 cells | INS | targetBased | 127961 | 1153 | type II hypersensitivity reaction disease | 0.252318308693775 | 686 |
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_interaction | targetBased | 359207 | 1432 | lymphatic system disease | 0.256421443619648 | 118 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | pathwayBased | 70898 | 707 | lymphatic system disease | 0.261338183572329 | 27 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | pathwayBased | 131324 | 544 | lymphatic system disease | 0.261338183572329 | 27 |
EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Reader - 2125-01_Inhibitor_SinglePoint_HTS_Activity | EZH2_inhibitors | targetBased | 57013 | 201 | lymphatic system disease | 0.258343187398969 | 363 |
qHTS Assay for NPC1 Promoter Activators | NPC1 | pathwayBased | 320682 | 7575 | lymphatic system disease | 0.303994030836414 | 1315 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | lymphatic system disease | 0.286395979852275 | 244 |
HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | HRAS | targetBased | 194628 | 267 | lymphatic system disease | 0.270951962053554 | 24 |
HTS identification of compounds activating phosphomannose isomerase (PMI) via a fluorescence intensity assay using a near- saturating concentration of mannose 6-phosphat | MPI | targetBased | 194152 | 656 | lymphatic system disease | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate | MPI | targetBased | 194152 | 1288 | lymphatic system disease | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | MPI | targetBased | 194152 | 814 | lymphatic system disease | 0.307418870150215 | 258 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | hypersensitivity reaction disease | 0.302054926818412 | 443 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | hypersensitivity reaction disease | 0.302054926818412 | 443 |
uHTS luminescence assay for the identification of compounds that inhibit NOD2 | NOD2 | targetBased | 292323 | 1836 | hypersensitivity reaction disease | 0.314702437973755 | 696 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | targetBased | 359207 | 1189 | hypersensitivity reaction disease | 0.250619928589118 | 12 |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | targetBased | 63676 | 1938 | hypersensitivity reaction disease | 0.250619928589118 | 12 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | targetBased | 359207 | 316 | hypersensitivity reaction disease | 0.250619928589118 | 12 |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | targetBased | 63656 | 2179 | hypersensitivity reaction disease | 0.250619928589118 | 12 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | targetBased | 359207 | 4555 | hypersensitivity reaction disease | 0.250619928589118 | 12 |
Primary screen for compounds that activate Insulin promoter activity in TRM-6 cells | INS | targetBased | 128695 | 1039 | hypersensitivity reaction disease | 0.252347407467467 | 688 |
Primary screen for compounds that inhibit Insulin promoter activity in TRM-6 cells | INS | targetBased | 127961 | 1153 | hypersensitivity reaction disease | 0.252347407467467 | 688 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | targetBased | 217959 | 2390 | Abnormality of the immune system | 0.250738061112055 | 218 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | autoimmune disorder of gastrointestinal tract | 0.300515512262878 | 317 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | autoimmune disorder of gastrointestinal tract | 0.300515512262878 | 317 |
Primary screen for compounds that activate Insulin promoter activity in TRM-6 cells | INS | targetBased | 128695 | 1039 | autoimmune disorder of gastrointestinal tract | 0.252080447239734 | 669 |
Primary screen for compounds that inhibit Insulin promoter activity in TRM-6 cells | INS | targetBased | 127961 | 1153 | autoimmune disorder of gastrointestinal tract | 0.252080447239734 | 669 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | B cell deficiency | 0.278059242305738 | 204 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | B cell deficiency | 0.278059242305738 | 204 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | B cell deficiency | 0.293415424309692 | 203 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | B cell deficiency | 0.302045929993097 | 412 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | B cell deficiency | 0.302045929993097 | 412 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | hyperimmunoglobulin syndrome | 0.293054070786579 | 147 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | hyperimmunoglobulin syndrome | 0.302015873224594 | 392 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | hyperimmunoglobulin syndrome | 0.302015873224594 | 392 |
uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | targetBased | 330392 | 1295 | inborn error of immunity | 0.266884082183738 | 47 |
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_interaction | targetBased | 359207 | 1432 | leukocyte disorder | 0.265940944674663 | 211 |
EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Reader - 2125-01_Inhibitor_SinglePoint_HTS_Activity | EZH2_inhibitors | targetBased | 57013 | 201 | leukocyte disorder | 0.274948506767873 | 418 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | leukocyte disorder | 0.281347845545978 | 1325 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | leukocyte disorder | 0.281347845545978 | 1325 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | leukocyte disorder | 0.293880056330526 | 368 |
qHTS assay for re-activators of p53 using a Luc reporter | TP53 | pathwayBased | 321427 | 201 | leukocyte disorder | 0.293944069536877 | 1499 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54509 | 528 | leukocyte disorder | 0.293944069536877 | 1499 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54513 | 338 | leukocyte disorder | 0.293944069536877 | 1499 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 125394 | 1890 | leukocyte disorder | 0.293944069536877 | 1499 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 124022 | 1156 | leukocyte disorder | 0.293944069536877 | 1499 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | leukocyte disorder | 0.289127425827789 | 314 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | leukocyte disorder | 0.29708712507018 | 546 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | leukocyte disorder | 0.315033846306356 | 958 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | leukocyte disorder | 0.315033846306356 | 958 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | immune deficiency disease | 0.282900280866123 | 400 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | immune deficiency disease | 0.282900280866123 | 400 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | immune deficiency disease | 0.293434735083632 | 275 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | immune deficiency disease | 0.280530062736223 | 151 |
uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | targetBased | 330392 | 1295 | immune deficiency disease | 0.266884082183738 | 47 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | immune deficiency disease | 0.302049368982857 | 458 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | immune deficiency disease | 0.302049368982857 | 458 |
qHTS Assay for NPC1 Promoter Activators | NPC1 | pathwayBased | 320682 | 7575 | non-Langerhans cell histiocytosis | 0.303994027521701 | 1314 |
High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Primary Screen | NFKB1 | pathwayBased | 193265 | 3100 | syndromic agammaglobulinemia | 0.278029312774993 | 118 |
uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay | NFKB1 | pathwayBased | 359244 | 3094 | syndromic agammaglobulinemia | 0.278029312774993 | 118 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | functional neutrophil defect | 0.296879875982787 | 441 |
HTS identification of compounds activating phosphomannose isomerase (PMI) via a fluorescence intensity assay using a near- saturating concentration of mannose 6-phosphat | MPI | targetBased | 194152 | 656 | primary lymphedema | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate | MPI | targetBased | 194152 | 1288 | primary lymphedema | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | MPI | targetBased | 194152 | 814 | primary lymphedema | 0.307418870150215 | 258 |
HTS identification of compounds activating phosphomannose isomerase (PMI) via a fluorescence intensity assay using a near- saturating concentration of mannose 6-phosphat | MPI | targetBased | 194152 | 656 | lymphedema | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate | MPI | targetBased | 194152 | 1288 | lymphedema | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | MPI | targetBased | 194152 | 814 | lymphedema | 0.307418870150215 | 258 |
HTS identification of compounds activating phosphomannose isomerase (PMI) via a fluorescence intensity assay using a near- saturating concentration of mannose 6-phosphat | MPI | targetBased | 194152 | 656 | lymphatic malformation | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate | MPI | targetBased | 194152 | 1288 | lymphatic malformation | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | MPI | targetBased | 194152 | 814 | lymphatic malformation | 0.307418870150215 | 258 |
qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | BLM_inhibitors | targetBased | 347933 | 673 | microcephaly, growth restriction and increased sister chromatid exchange | 0.312126707883687 | 1978 |
Primary qHTS assay for inhibitors of Activation Induced Cytidine Deaminase (AID): AID signal | AICDA_inhibitors | targetBased | 90878 | 289 | immunodeficiency disease | 0.293439877042445 | 345 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | immunodeficiency disease | 0.326988384067494 | 13299 |
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_interaction | targetBased | 359207 | 1432 | lymphoid system disorder | 0.256421443619648 | 118 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | pathwayBased | 70898 | 707 | lymphoid system disorder | 0.261338183572329 | 27 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | pathwayBased | 131324 | 544 | lymphoid system disorder | 0.261338183572329 | 27 |
EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Reader - 2125-01_Inhibitor_SinglePoint_HTS_Activity | EZH2_inhibitors | targetBased | 57013 | 201 | lymphoid system disorder | 0.258343187398969 | 363 |
qHTS Assay for NPC1 Promoter Activators | NPC1 | pathwayBased | 320682 | 7575 | lymphoid system disorder | 0.303994030836414 | 1315 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | lymphoid system disorder | 0.286395979852275 | 244 |
HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | HRAS | targetBased | 194628 | 267 | lymphoid system disorder | 0.270955346870825 | 25 |
HTS identification of compounds activating phosphomannose isomerase (PMI) via a fluorescence intensity assay using a near- saturating concentration of mannose 6-phosphat | MPI | targetBased | 194152 | 656 | lymphoid system disorder | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate | MPI | targetBased | 194152 | 1288 | lymphoid system disorder | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | MPI | targetBased | 194152 | 814 | lymphoid system disorder | 0.307418870150215 | 258 |
uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | artemis_inhibitors | targetBased | 30104 | 235 | familial severe combined immunodeficiency | 0.30736672335538 | 539 |
qHTS assay for re-activators of p53 using a Luc reporter | TP53 | pathwayBased | 321427 | 201 | lymphoid system disorder | 0.28981872771125 | 1409 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54509 | 528 | lymphoid system disorder | 0.28981872771125 | 1409 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 54513 | 338 | lymphoid system disorder | 0.28981872771125 | 1409 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 125394 | 1890 | lymphoid system disorder | 0.28981872771125 | 1409 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | targetBased | 124022 | 1156 | lymphoid system disorder | 0.28981872771125 | 1409 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | Primary immunodeficiency due to a defect in innate immunity | 0.308814750112337 | 560 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | Primary immunodeficiency due to a defect in innate immunity | 0.308814750112337 | 560 |
HTS identification of compounds inhibiting the binding of CD11b/CD18 to fibrinogen via a luminescence assay. | ITGB2 | targetBased | 92518 | 501 | Primary immunodeficiency due to a defect in innate immunity | 0.280428462857787 | 42 |
uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | targetBased | 330392 | 1295 | Primary immunodeficiency due to a defect in innate immunity | 0.266507580720034 | 22 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | Genetic susceptibility to infections due to particular pathogens | 0.308738055196523 | 545 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | Genetic susceptibility to infections due to particular pathogens | 0.308738055196523 | 545 |
qHTS Assay for Identifying a Potential Treatment of Ataxia-Telangiectasia | ATM_modulators | targetBased | 322361 | 619 | DNA repair defect other than combined T-cell and B-cell immunodeficiencies | 0.321645326286388 | 6829 |
Primary cell-based high throughput screening assay to measure STAT1 activation | STAT1 activation | pathwayBased | 195980 | 5134 | Genetic immune deficiency with skin involvement | 0.299233459881725 | 277 |
Primary cell-based high throughput screening assay to measure STAT1 inhibition | STAT1 | targetBased | 195980 | 695 | Genetic immune deficiency with skin involvement | 0.299233459881725 | 277 |
Primary cell-based high throughput screening assay to measure STAT3 activation | STAT3 | pathwayBased | 194666 | 1772 | Genetic immune deficiency with skin involvement | 0.294031557794827 | 422 |
Primary cell-based high throughput screening assay to measure STAT3 inhibition | STAT3 | pathwayBased | 194666 | 1722 | Genetic immune deficiency with skin involvement | 0.294031557794827 | 422 |
uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | targetBased | 330392 | 1295 | Autoinflammatory syndrome with immune deficiency | 0.26595669758817 | 16 |
Some of these associations have also gone through clinical trials, as those in the graph below.
graph
Find clinical trials details in table. Use scroll bar or search funtion to select specific drugs, molecular targets or diseases.
table