OpenTargets offers > 19k target-disease associations from PChem targets suitable for virtual screening based in OpenTargets scores for cardiovascular disorders. See here the best scored pairs.
Check best scored target-disease associations in table:
PubChemAssay | program | diseaseName | assayType | testedComopunds | activeCompounds | weightedScore | weightedEvidence |
---|---|---|---|---|---|---|---|
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | congestive heart failure | targetBased | 335239 | 801 | 0.351769550612851 | 13 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | congestive heart failure | targetBased | 335238 | 390 | 0.351769550612851 | 13 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | congestive heart failure | targetBased | 335531 | 328 | 0.527581485904718 | 6 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | congestive heart failure | targetBased | 339297 | 1446 | 0.651600017001438 | 50 |
Natriuretic polypeptide receptor (hNpr1) antagonism - Primary qHTS | NPR1 | congestive heart failure | targetBased | 76168 | 1231 | 0.613250657387013 | 22 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | atrial fibrillation | targetBased | 305610 | 3878 | 0.541829820157546 | 315 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | atrial fibrillation | targetBased | 305610 | 1082 | 0.541829820157546 | 315 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | atrial fibrillation | targetBased | 305610 | 1552 | 0.802439563669594 | 261 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | atrial fibrillation | targetBased | 343666 | 1267 | 0.802439563669594 | 261 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | atrial fibrillation | targetBased | 342084 | 3260 | 0.802439563669594 | 261 |
Factor XIa 1536 HTS | F11_modulation | atrial fibrillation | targetBased | 218707 | 302 | 0.357517588702518 | 23 |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | atrial fibrillation | targetBased | 405130 | 6428 | 0.420727514448716 | 59 |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | atrial fibrillation | targetBased | 373462 | 23 | 0.420727514448716 | 59 |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | atrial fibrillation | targetBased | 405130 | 6428 | 0.420727514448716 | 59 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | atrial fibrillation | targetBased | 305610 | 2592 | 0.783777345668684 | 234 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | atrial fibrillation | targetBased | 86095 | 1114 | 0.539624047756777 | 26 |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | atrial fibrillation | targetBased | 276265 | 806 | 0.424659611479414 | 15 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | atrial fibrillation | targetBased | 335531 | 328 | 0.670494073297023 | 97 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | atrial fibrillation | targetBased | 339297 | 1446 | 0.656155319809075 | 74 |
Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) | PTK2 | atrial fibrillation | targetBased | 96879 | 811 | 0.348342323787707 | 21 |
Thrombin 1536 HTS | F2_modulation | atrial fibrillation | targetBased | 217233 | 557 | 0.673166313522287 | 170 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | atrial fibrillation | pathwayBased | 271402 | 1048 | 0.334098389930725 | 11 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | atrial fibrillation | pathwayBased | 267412 | 5703 | 0.334098389930725 | 11 |
qHTS Assay for Tau Filament Binding | MAPT | atrial fibrillation | targetBased | 69668 | 1391 | 0.334098389930725 | 11 |
HCS assay for microtubule stabilizers | TUBB | atrial fibrillation | targetBased | 195821 | 1625 | 0.435406862853961 | 17 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | hypertension | targetBased | 86095 | 1442 | 0.421637500320573 | 54 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | hypertension | targetBased | 86095 | 1151 | 0.421637500320573 | 54 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | hypertension | targetBased | 394050 | 3624 | 0.50567174512419 | 25 |
Primary cell-based high-throughput screening for identification of compounds that inhibit/block calcium-activated chloride channels (TMEM16A) | ANO1_inhibitors | hypertension | targetBased | 306502 | 3633 | 0.304005649962294 | 22 |
Primary cell-based high-throughput screening for identification of compounds that activate/potentiate calcium-activated chloride channels (TMEM16A) | ANO1_activators | hypertension | targetBased | 335180 | 1022 | 0.304005649962294 | 22 |
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 | hypertension | targetBased | 99314 | 335 | 0.383046446409166 | 146 |
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 | hypertension | targetBased | 196176 | 782 | 0.383046446409166 | 146 |
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 | hypertension | targetBased | 99314 | 390 | 0.383046446409166 | 146 |
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 | hypertension | targetBased | 196177 | 811 | 0.383046446409166 | 146 |
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 | hypertension | targetBased | 196176 | 670 | 0.383046446409166 | 146 |
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 | hypertension | targetBased | 196177 | 519 | 0.383046446409166 | 146 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | hypertension | targetBased | 86095 | 1114 | 0.293898359792957 | 13 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | hypertension | targetBased | 335531 | 328 | 0.784665512239552 | 1291 |
MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity | ERAP1_inhibitors | hypertension | targetBased | 335777 | 499 | 0.436366272016687 | 11 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | hypertension | targetBased | 339297 | 1446 | 0.668853049947844 | 367 |
Natriuretic polypeptide receptor (hNpr1) antagonism - Primary qHTS | NPR1 | hypertension | targetBased | 76168 | 1231 | 0.565070002375135 | 27 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | hypertension | targetBased | 339674 | 2841 | 0.674429375550638 | 181 |
Allosteric Modulators of D1 Receptors: Primary Screen | D1 | hypertension | targetBased | 57705 | 3413 | 0.512185146348314 | 6 |
Allosteric Agonists of the Human D1 Dopamine Receptor: qHTS | D1_activators | hypertension | targetBased | 361330 | 3713 | 0.512185146348314 | 6 |
Antagonist of Human D 1 Dopamine Receptor: qHTS | D1_inhibitors | hypertension | targetBased | 355805 | 11440 | 0.512185146348314 | 6 |
Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | CACNA1H_inhibitors | hypertension | targetBased | 104728 | 4230 | 0.343100200487281 | 7 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | hypertension | targetBased | 316642 | 617 | 0.542390725803381 | 20 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | myocardial infarction | targetBased | 305610 | 1552 | 0.359248840869334 | 21 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | myocardial infarction | targetBased | 343666 | 1267 | 0.359248840869334 | 21 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | myocardial infarction | targetBased | 342084 | 3260 | 0.359248840869334 | 21 |
HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Inhibitor_SinglePoint_HTS_Activity | SCARB1 | myocardial infarction | targetBased | 319204 | 3065 | 0.379088804549568 | 72 |
HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity | SCARB1 | myocardial infarction | targetBased | 316970 | 306 | 0.379088804549568 | 72 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | myocardial infarction | targetBased | 86095 | 1442 | 0.339277341652025 | 118 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | myocardial infarction | targetBased | 86095 | 1151 | 0.339277341652025 | 118 |
qHTS for Inhibitors of TGF-b | TGFB1 | myocardial infarction | pathwayBased | 403345 | 4970 | 0.32105894859906 | 913 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | myocardial infarction | targetBased | 394050 | 3624 | 0.376253753005692 | 31 |
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 | myocardial infarction | targetBased | 335239 | 991 | 0.578271542280002 | 11 |
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 | myocardial infarction | targetBased | 335239 | 695 | 0.578271542280002 | 11 |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | myocardial infarction | targetBased | 405130 | 6428 | 0.555353879811961 | 333 |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | myocardial infarction | targetBased | 373462 | 23 | 0.555353879811961 | 333 |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | myocardial infarction | targetBased | 405130 | 6428 | 0.555353879811961 | 333 |
qHTS for Inhibitors of Cell Surface uPA Generation | PLAU | myocardial infarction | targetBased | 325247 | 1021 | 0.418499778482598 | 30 |
Primary biochemical high-throughput screening assay for inhibitors of Rho kinase 2 (Rhok2) | ROCK2 | myocardial infarction | targetBased | 59788 | 212 | 0.408625509213493 | 11 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | myocardial infarction | targetBased | 86095 | 1114 | 0.294234899440742 | 38 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | myocardial infarction | targetBased | 359518 | 300 | 0.439839067210336 | 6 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | myocardial infarction | targetBased | 335652 | 1779 | 0.439839067210336 | 6 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | myocardial infarction | targetBased | 362274 | 1056 | 0.439839067210336 | 6 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | myocardial infarction | targetBased | 336308 | 6862 | 0.439839067210336 | 6 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | myocardial infarction | targetBased | 357537 | 806 | 0.439839067210336 | 6 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | myocardial infarction | targetBased | 339887 | 1178 | 0.439839067210336 | 6 |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | myocardial infarction | targetBased | 276265 | 806 | 0.355475691441654 | 6 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | myocardial infarction | targetBased | 335531 | 328 | 0.659633610265158 | 76 |
HTS of Smad transcription factor inhibitors | SMAD3 | myocardial infarction | targetBased | 88033 | 251 | 0.430244164060686 | 118 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | myocardial infarction | targetBased | 339297 | 1446 | 0.670611093215975 | 227 |
Thrombin 1536 HTS | F2_modulation | myocardial infarction | targetBased | 217233 | 557 | 0.599407497681816 | 152 |
HCS assay for microtubule stabilizers | TUBB | myocardial infarction | targetBased | 195821 | 1625 | 0.581891484264645 | 13 |
Primary qHTS for Inhibitors of ATXN expression | ATXN2_repressors | myocardial infarction | targetBased | 358434 | 2554 | 0.307714483936324 | 20 |
HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Inhibitor_SinglePoint_HTS_Activity | SCARB1 | coronary artery disease | targetBased | 319204 | 3065 | 0.513875832928574 | 147 |
HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity | SCARB1 | coronary artery disease | targetBased | 316970 | 306 | 0.513875832928574 | 147 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | coronary artery disease | targetBased | 86095 | 1442 | 0.470428412517821 | 183 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | coronary artery disease | targetBased | 86095 | 1151 | 0.470428412517821 | 183 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | coronary artery disease | targetBased | 363803 | 2412 | 0.414572866969997 | 13 |
qHTS for Inhibitors of TGF-b | TGFB1 | coronary artery disease | pathwayBased | 403345 | 4970 | 0.376449062041855 | 224 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | coronary artery disease | targetBased | 394050 | 3624 | 0.387861128233729 | 70 |
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 | coronary artery disease | targetBased | 335239 | 991 | 0.592008485412301 | 10 |
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 | coronary artery disease | targetBased | 335239 | 695 | 0.592008485412301 | 10 |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | coronary artery disease | targetBased | 405130 | 6428 | 0.384469301589397 | 153 |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | coronary artery disease | targetBased | 373462 | 23 | 0.384469301589397 | 153 |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | coronary artery disease | targetBased | 405130 | 6428 | 0.384469301589397 | 153 |
qHTS for Inhibitors of Cell Surface uPA Generation | PLAU | coronary artery disease | targetBased | 325247 | 1021 | 0.411957572558763 | 21 |
Fluorescence-based biochemical high throughput primary assay to identify inhibitors of phospholipase C isozymes (PLC-gamma1). | PLCG1 | coronary artery disease | targetBased | 369953 | 3123 | 0.266582952262131 | 6 |
Screen for inhibitors of the SWI/SNF chromatin remodeling complex (esBAF) in mouse embryonic stem cells with Luciferase reporter assay Measured in Cell-Based System Using Plate Reader - 2141-01_Inhibitor_SinglePoint_HTS_Activity | SMARCA4 | coronary artery disease | targetBased | 344733 | 7043 | 0.277611256410927 | 45 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | coronary artery disease | targetBased | 335239 | 801 | 0.452107414048022 | 599 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | coronary artery disease | targetBased | 335238 | 390 | 0.452107414048022 | 599 |
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 | coronary artery disease | targetBased | 99314 | 335 | 0.538184411305718 | 204 |
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 | coronary artery disease | targetBased | 196176 | 782 | 0.538184411305718 | 204 |
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 | coronary artery disease | targetBased | 99314 | 390 | 0.538184411305718 | 204 |
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 | coronary artery disease | targetBased | 196177 | 811 | 0.538184411305718 | 204 |
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 | coronary artery disease | targetBased | 196176 | 670 | 0.538184411305718 | 204 |
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 | coronary artery disease | targetBased | 196177 | 519 | 0.538184411305718 | 204 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | coronary artery disease | targetBased | 86095 | 1114 | 0.440700143257634 | 29 |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | coronary artery disease | targetBased | 276265 | 806 | 0.375083156200627 | 6 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | coronary artery disease | targetBased | 335531 | 328 | 0.666430352142117 | 442 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the HTRA serine peptidase 1 (HTRA1) | HTRA1 | coronary artery disease | targetBased | 343467 | 1710 | 0.445363479109043 | 10 |
Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | MC4R | coronary artery disease | targetBased | 356160 | 3470 | 0.39314131155056 | 20 |
TRFRET-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): antagonists of MC4R | MC4R | coronary artery disease | targetBased | 356160 | 1703 | 0.39314131155056 | 20 |
HTS of Smad transcription factor inhibitors | SMAD3 | coronary artery disease | targetBased | 88033 | 251 | 0.552484115357613 | 54 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | coronary artery disease | targetBased | 339297 | 1446 | 0.614742335189791 | 48 |
Natriuretic polypeptide receptor (hNpr1) antagonism - Primary qHTS | NPR1 | coronary artery disease | targetBased | 76168 | 1231 | 0.435439202613319 | 10 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | coronary artery disease | targetBased | 305610 | 3794 | 0.601498428437273 | 11 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | coronary artery disease | targetBased | 339674 | 2841 | 0.601498428437273 | 11 |
Thrombin 1536 HTS | F2_modulation | coronary artery disease | targetBased | 217233 | 557 | 0.649046640119132 | 118 |
HCS assay for microtubule stabilizers | TUBB | coronary artery disease | targetBased | 195821 | 1625 | 0.641765925028877 | 28 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | coronary artery disease | targetBased | 316642 | 617 | 0.440994765306032 | 15 |
Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | TLR9 | coronary artery disease | targetBased | 343468 | 734 | 0.513031657023707 | 18 |
HTS of Smad transcription factor inhibitors | SMAD3 | aortic aneurysm | targetBased | 88033 | 251 | 0.501060091567992 | 63 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | heart disease | targetBased | 305610 | 3878 | 0.336382820641752 | 2001 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | heart disease | targetBased | 305610 | 1082 | 0.336382820641752 | 2001 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | heart disease | targetBased | 305610 | 1552 | 0.5744892428341 | 1627 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | heart disease | targetBased | 343666 | 1267 | 0.5744892428341 | 1627 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | heart disease | targetBased | 342084 | 3260 | 0.5744892428341 | 1627 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | heart disease | targetBased | 86095 | 1442 | 0.491789587663523 | 249 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | heart disease | targetBased | 86095 | 1151 | 0.491789587663523 | 249 |
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 | heart disease | targetBased | 335239 | 991 | 0.610101705726402 | 24 |
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 | heart disease | targetBased | 335239 | 695 | 0.610101705726402 | 24 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | heart disease | targetBased | 305610 | 2592 | 0.337779720181742 | 1164 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | heart disease | targetBased | 335239 | 801 | 0.388259441397677 | 2598 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | heart disease | targetBased | 335238 | 390 | 0.388259441397677 | 2598 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | heart disease | targetBased | 86095 | 1114 | 0.482009080109138 | 883 |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | heart disease | targetBased | 276265 | 806 | 0.420322702524328 | 19 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | heart disease | targetBased | 335531 | 328 | 0.593237032510884 | 412 |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | heart disease | targetBased | 324747 | 813 | 0.400381769027036 | 16 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | heart disease | targetBased | 339297 | 1446 | 0.48950855104779 | 265 |
Natriuretic polypeptide receptor (hNpr1) antagonism - Primary qHTS | NPR1 | heart disease | targetBased | 76168 | 1231 | 0.494409718878496 | 153 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | KCNK9_blockers | heart disease | targetBased | 305610 | 3794 | 0.494040568817361 | 17 |
qHTS Assay for Activators of Human alpha-Glucosidase as a Potential Chaperone Treatment of Pompe Disease | GAA | heart disease | targetBased | 199169 | 715 | 0.329286693560426 | 3157 |
qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | GAA_inhibitors | heart disease | targetBased | 302297 | 1165 | 0.329286693560426 | 3157 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | heart disease | targetBased | 339674 | 2841 | 0.527003319061794 | 45 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn6) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | heart disease | targetBased | 369953 | 760 | 0.442491548090815 | 45 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn7) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | heart disease | targetBased | 369953 | 498 | 0.442491548090815 | 45 |
Glucocerebrosidase | GBA1 | heart disease | targetBased | 48118 | 549 | 0.295851471883425 | 192 |
Thrombin 1536 HTS | F2_modulation | heart disease | targetBased | 217233 | 557 | 0.439971747608358 | 209 |
HCS assay for microtubule stabilizers | TUBB | heart disease | targetBased | 195821 | 1625 | 0.274582164904876 | 34 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | heart failure | targetBased | 305610 | 1552 | 0.547212563446782 | 10 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | heart failure | targetBased | 343666 | 1267 | 0.547212563446782 | 10 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | heart failure | targetBased | 342084 | 3260 | 0.547212563446782 | 10 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | heart failure | targetBased | 394050 | 3624 | 0.537056766771359 | 15 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | heart failure | targetBased | 335239 | 801 | 0.64314305161478 | 117 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | heart failure | targetBased | 335238 | 390 | 0.64314305161478 | 117 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | heart failure | targetBased | 335531 | 328 | 0.645161667574849 | 44 |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | heart failure | targetBased | 324747 | 813 | 0.582667962238769 | 9 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | heart failure | targetBased | 339297 | 1446 | 0.660625331502392 | 81 |
Natriuretic polypeptide receptor (hNpr1) antagonism - Primary qHTS | NPR1 | heart failure | targetBased | 76168 | 1231 | 0.597582643776577 | 29 |
qHTS Assay for Antagonists of the Relaxin Receptor RXFP1 | relaxinInhibitors | heart failure | targetBased | 350177 | 2058 | 0.402671409429789 | 15 |
qHTS Assay for Antagonists of the Relaxin Receptor RXFP1Taking the negative queue for PMs | relaxin PMs | heart failure | targetBased | 350177 | 2058 | 0.402671409429789 | 15 |
qHTS Assay for Agonists of the Relaxin Receptor RXFP1 | RXFP1 | heart failure | targetBased | 362198 | 1084 | 0.402671409429789 | 15 |
HCS assay for microtubule stabilizers | TUBB | heart failure | targetBased | 195821 | 1625 | 0.366142497875815 | 6 |
Factor XIa 1536 HTS | F11_modulation | pulmonary embolism | targetBased | 218707 | 302 | 0.529837764887743 | 9 |
Thrombin 1536 HTS | F2_modulation | pulmonary embolism | targetBased | 217233 | 557 | 0.630479729710024 | 26 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | atrial flutter | targetBased | 305610 | 1552 | 0.561048672319976 | 20 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | atrial flutter | targetBased | 343666 | 1267 | 0.561048672319976 | 20 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | atrial flutter | targetBased | 342084 | 3260 | 0.561048672319976 | 20 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | atrial flutter | targetBased | 335531 | 328 | 0.529463532047883 | 9 |
qHTS for Inhibitors of TGF-b | TGFB1 | angina pectoris | pathwayBased | 403345 | 4970 | 0.291232525916009 | 30 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | angina pectoris | targetBased | 335531 | 328 | 0.662387380315676 | 134 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | angina pectoris | targetBased | 339297 | 1446 | 0.615165132654478 | 23 |
qHTS for Inhibitors of Inflammasome Signaling: IL-1-beta AlphaLISA Primary Screen | IL-1b Inflammasome | atherosclerosis | pathwayBased | 362051 | 17187 | 0.307719686617144 | 1501 |
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 | atherosclerosis | targetBased | 99314 | 335 | 0.431128940589068 | 990 |
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 | atherosclerosis | targetBased | 196176 | 782 | 0.431128940589068 | 990 |
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 | atherosclerosis | targetBased | 99314 | 390 | 0.431128940589068 | 990 |
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 | atherosclerosis | targetBased | 196177 | 811 | 0.431128940589068 | 990 |
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 | atherosclerosis | targetBased | 196176 | 670 | 0.431128940589068 | 990 |
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 | atherosclerosis | targetBased | 196177 | 519 | 0.431128940589068 | 990 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | PLA2G7 | atherosclerosis | targetBased | 326024 | 4934 | 0.344157854845113 | 518 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | atherosclerosis | targetBased | 335531 | 328 | 0.388681972644248 | 6 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | atherosclerosis | targetBased | 339297 | 1446 | 0.523118463288717 | 14 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | left ventricular hypertrophy | targetBased | 394050 | 3624 | 0.28891104408561 | 29 |
HCS assay for microtubule stabilizers | TUBB | Coronary Restenosis | targetBased | 195821 | 1625 | 0.310920784693153 | 6 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | Coronary Vasospasm | targetBased | 335531 | 328 | 0.642829168666001 | 119 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | ventricular fibrillation | targetBased | 305610 | 1552 | 0.760259527871274 | 51 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | ventricular fibrillation | targetBased | 343666 | 1267 | 0.760259527871274 | 51 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | ventricular fibrillation | targetBased | 342084 | 3260 | 0.760259527871274 | 51 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ventricular fibrillation | targetBased | 339297 | 1446 | 0.411238352018758 | 12 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | vascular disease | targetBased | 86095 | 1442 | 0.259756508590195 | 420 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | vascular disease | targetBased | 86095 | 1151 | 0.259756508590195 | 420 |
Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | JAK2 | vascular disease | targetBased | 217959 | 2390 | 0.259257178462855 | 247 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | vascular disease | pathwayBased | 70898 | 707 | 0.26037973565382 | 72 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | vascular disease | pathwayBased | 131324 | 544 | 0.26037973565382 | 72 |
qHTS assay for re-activators of p53 using a Luc reporter | TP53 | vascular disease | pathwayBased | 321427 | 201 | 0.308282010064809 | 737 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | vascular disease | targetBased | 54509 | 528 | 0.308282010064809 | 737 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53 Null Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | vascular disease | targetBased | 54513 | 338 | 0.308282010064809 | 737 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | vascular disease | targetBased | 125394 | 1890 | 0.308282010064809 | 737 |
qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | nonSmallCellLungCarcinomaWithP53Mutations | vascular disease | targetBased | 124022 | 1156 | 0.308282010064809 | 737 |
Primary screen for compounds that activate Alzheimer's amyloid precursor | APP_inhibitors | vascular disease | pathwayBased | 193400 | 1987 | 0.322472728273551 | 337 |
Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | APP_inhibitors | vascular disease | pathwayBased | 193714 | 1590 | 0.322472728273551 | 337 |
qHTS for compounds that reverse cellular toxicity of Amyloid beta (A-beta) peptide in yeast: Primary Screen | APP_inhibitors | vascular disease | targetBased | 404343 | 257 | 0.322472728273551 | 337 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | vascular disease | targetBased | 335531 | 328 | 0.333129665796641 | 710 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the HTRA serine peptidase 1 (HTRA1) | HTRA1 | vascular disease | targetBased | 343467 | 1710 | 0.303404291721427 | 121 |
HTS of Smad transcription factor inhibitors | SMAD3 | vascular disease | targetBased | 88033 | 251 | 0.31738553424318 | 944 |
High Throughput Imaging Assay for Beta-Catenin | betaCateninTranslocation | vascular disease | targetBased | 193542 | 587 | 0.259830615135327 | 68 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | vascular disease | targetBased | 339297 | 1446 | 0.256542920788158 | 346 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | vascular disease | targetBased | 339674 | 2841 | 0.311051929154863 | 182 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn6) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | vascular disease | targetBased | 369953 | 760 | 0.25398423452813 | 69 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn7) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | vascular disease | targetBased | 369953 | 498 | 0.25398423452813 | 69 |
HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | HRAS | vascular disease | targetBased | 194628 | 267 | 0.281944830858339 | 35 |
Thrombin 1536 HTS | F2_modulation | vascular disease | targetBased | 217233 | 557 | 0.278048642860817 | 660 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | peripheral arterial disease | targetBased | 363803 | 2412 | 0.541518657430405 | 12 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | peripheral arterial disease | targetBased | 394050 | 3624 | 0.507918611603607 | 9 |
HCS assay for microtubule stabilizers | TUBB | peripheral arterial disease | targetBased | 195821 | 1625 | 0.366953918967478 | 8 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | cardiac arrhythmia | targetBased | 305610 | 3878 | 0.717418405216669 | 970 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | cardiac arrhythmia | targetBased | 305610 | 1082 | 0.717418405216669 | 970 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | cardiac arrhythmia | targetBased | 305610 | 1552 | 0.815852504474459 | 1310 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | cardiac arrhythmia | targetBased | 343666 | 1267 | 0.815852504474459 | 1310 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | cardiac arrhythmia | targetBased | 342084 | 3260 | 0.815852504474459 | 1310 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | cardiac arrhythmia | targetBased | 363803 | 2412 | 0.539628835168446 | 7 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | cardiac arrhythmia | targetBased | 305610 | 2592 | 0.597082684094759 | 166 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | cardiac arrhythmia | targetBased | 359518 | 300 | 0.542720161698728 | 8 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | cardiac arrhythmia | targetBased | 335652 | 1779 | 0.542720161698728 | 8 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | cardiac arrhythmia | targetBased | 362274 | 1056 | 0.542720161698728 | 8 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | cardiac arrhythmia | targetBased | 336308 | 6862 | 0.542720161698728 | 8 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | cardiac arrhythmia | targetBased | 357537 | 806 | 0.542720161698728 | 8 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | cardiac arrhythmia | targetBased | 339887 | 1178 | 0.542720161698728 | 8 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | cardiac arrhythmia | targetBased | 335531 | 328 | 0.604597373994676 | 52 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | cardiac arrhythmia | targetBased | 359207 | 1189 | 0.578250225184157 | 7 |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | cardiac arrhythmia | targetBased | 63676 | 1938 | 0.578250225184157 | 7 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | cardiac arrhythmia | targetBased | 359207 | 316 | 0.578250225184157 | 7 |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | cardiac arrhythmia | targetBased | 63656 | 2179 | 0.578250225184157 | 7 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | cardiac arrhythmia | targetBased | 359207 | 4555 | 0.578250225184157 | 7 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_agonists | cardiac arrhythmia | targetBased | 363803 | 502 | 0.580213188041739 | 7 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_antgonists | cardiac arrhythmia | targetBased | 363803 | 2629 | 0.580213188041739 | 7 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 4 (CHRM4) | CHRM4_PAMs | cardiac arrhythmia | targetBased | 363803 | 1450 | 0.580213188041739 | 7 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | cardiac arrhythmia | targetBased | 363803 | 698 | 0.577168330395272 | 6 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | cardiac arrhythmia | targetBased | 363803 | 2133 | 0.577168330395272 | 6 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human cholinergic receptor, muscarinic 5 (CHRM5) | CHRM5 | cardiac arrhythmia | targetBased | 363803 | 1081 | 0.577168330395272 | 6 |
qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | MAPT | cardiac arrhythmia | pathwayBased | 271402 | 1048 | 0.361351848709784 | 22 |
qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | MAPT | cardiac arrhythmia | pathwayBased | 267412 | 5703 | 0.361351848709784 | 22 |
qHTS Assay for Tau Filament Binding | MAPT | cardiac arrhythmia | targetBased | 69668 | 1391 | 0.361351848709784 | 22 |
HCS assay for microtubule stabilizers | TUBB | cardiac arrhythmia | targetBased | 195821 | 1625 | 0.335410282414491 | 7 |
Inhibitors of the vitamin D receptor (VDR): qHTS | VDR | blood pressure | targetBased | 394050 | 3624 | 0.308553519683985 | 6 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | blood pressure | targetBased | 335531 | 328 | 0.406928483573352 | 17 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | blood pressure | targetBased | 339674 | 2841 | 0.445041065782812 | 28 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | electrocardiography | targetBased | 305610 | 3878 | 0.590050079226244 | 203 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | electrocardiography | targetBased | 305610 | 1082 | 0.590050079226244 | 203 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | electrocardiography | targetBased | 305610 | 1552 | 0.431082166107401 | 54 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | electrocardiography | targetBased | 343666 | 1267 | 0.431082166107401 | 54 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | electrocardiography | targetBased | 342084 | 3260 | 0.431082166107401 | 54 |
uHTS identification of HIF-2a Inhibitors in a luminesence assay | HIF-2a_inhibitors | electrocardiography | targetBased | 363840 | 2624 | 0.527705179950392 | 17 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | electrocardiography | targetBased | 305610 | 2592 | 0.451022018543145 | 59 |
Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) | NCOA2 | electrocardiography | targetBased | 368927 | 620 | 0.445812129516972 | 35 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | sudden cardiac arrest | targetBased | 305610 | 1552 | 0.459752810561344 | 20 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | sudden cardiac arrest | targetBased | 343666 | 1267 | 0.459752810561344 | 20 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | sudden cardiac arrest | targetBased | 342084 | 3260 | 0.459752810561344 | 20 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | sudden cardiac arrest | targetBased | 339297 | 1446 | 0.647528186233432 | 36 |
HTS of Smad transcription factor inhibitors | SMAD3 | thoracic aortic aneurysm | targetBased | 88033 | 251 | 0.329835797553122 | 35 |
Factor XIa 1536 HTS | F11_modulation | venous thromboembolism | targetBased | 218707 | 302 | 0.660405165989325 | 101 |
Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | THRB | electrocardiography | targetBased | 276265 | 806 | 0.487395272317986 | 19 |
Thrombin 1536 HTS | F2_modulation | venous thromboembolism | targetBased | 217233 | 557 | 0.704341553035662 | 518 |
HCS assay for microtubule stabilizers | TUBB | vascular disease | targetBased | 195821 | 1625 | 0.272405235445476 | 36 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | cardiac arrhythmia | targetBased | 339297 | 1446 | 0.637646823165619 | 67 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | QT interval | targetBased | 305610 | 3878 | 0.596223074271587 | 24 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | QT interval | targetBased | 305610 | 1082 | 0.596223074271587 | 24 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | QT interval | targetBased | 305610 | 1552 | 0.449874560758587 | 18 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | QT interval | targetBased | 343666 | 1267 | 0.449874560758587 | 18 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | QT interval | targetBased | 342084 | 3260 | 0.449874560758587 | 18 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | QT interval | targetBased | 305610 | 2592 | 0.348212042945037 | 12 |
HTS of Smad transcription factor inhibitors | SMAD3 | intraocular pressure measurement | targetBased | 88033 | 251 | 0.473819659941471 | 9 |
Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) | NCOA2 | cardiac troponin T measurement | targetBased | 368927 | 620 | 0.429531803958325 | 6 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | congenital heart disease | targetBased | 305610 | 1552 | 0.27185250121656 | 332 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | congenital heart disease | targetBased | 343666 | 1267 | 0.27185250121656 | 332 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | congenital heart disease | targetBased | 342084 | 3260 | 0.27185250121656 | 332 |
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 | congenital heart disease | targetBased | 359207 | 1432 | 0.523986132818436 | 18 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | congenital heart disease | pathwayBased | 70898 | 707 | 0.532266653827459 | 10 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | congenital heart disease | pathwayBased | 131324 | 544 | 0.532266653827459 | 10 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | congenital heart disease | targetBased | 339297 | 1446 | 0.355696532380639 | 8 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | congenital heart disease | targetBased | 339674 | 2841 | 0.516813251834099 | 7 |
Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of COUP-TFII (NR2F2) | NR2F2 | congenital heart disease | targetBased | 369953 | 2602 | 0.798914888419431 | 147 |
Factor XIa 1536 HTS | F11_modulation | acute coronary syndrome | targetBased | 218707 | 302 | 0.284450312827731 | 11 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | pulse pressure measurement | targetBased | 86095 | 1442 | 0.465211580389372 | 11 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | pulse pressure measurement | targetBased | 86095 | 1151 | 0.465211580389372 | 11 |
Luminescence cell-based high throughput primary assay to identify inhibitors of TEAD-YAP interaction. | YAP1 | pulse pressure measurement | targetBased | 639428 | 9218 | 0.508571324863295 | 6 |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | acute coronary syndrome | targetBased | 405130 | 6428 | 0.286544845943286 | 26 |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | acute coronary syndrome | targetBased | 373462 | 23 | 0.286544845943286 | 26 |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | acute coronary syndrome | targetBased | 405130 | 6428 | 0.286544845943286 | 26 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | PLA2G7 | acute coronary syndrome | targetBased | 326024 | 4934 | 0.288472534590608 | 80 |
CYP2C19 Assay | CYP2C19_inhibitors | acute coronary syndrome | targetBased | 95857 | 20295 | 0.466037961739569 | 216 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | acute coronary syndrome | targetBased | 339297 | 1446 | 0.554062551323282 | 11 |
Thrombin 1536 HTS | F2_modulation | acute coronary syndrome | targetBased | 217233 | 557 | 0.58681113834509 | 26 |
HCS assay for microtubule stabilizers | TUBB | acute coronary syndrome | targetBased | 195821 | 1625 | 0.584323923650328 | 11 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | pulse pressure measurement | targetBased | 339674 | 2841 | 0.44919567405545 | 14 |
qHTS for Small Molecule Agonists and Allosteric Enhancers of Human TRH Receptor: Primary Screen for Agonists. | TRHR | pulse pressure measurement | targetBased | 361330 | 651 | 0.453922410273476 | 6 |
qHTS for Small Molecule Agonists and Allosteric Enhancers of Human TRH Receptor: Primary Screen for Enhancers | TRHR | pulse pressure measurement | targetBased | 361330 | 2424 | 0.453922410273476 | 6 |
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 | hypotension | targetBased | 335239 | 991 | 0.562382434947179 | 9 |
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 | hypotension | targetBased | 335239 | 695 | 0.562382434947179 | 9 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | hypotension | targetBased | 339297 | 1446 | 0.6612423935077 | 103 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | orthostatic hypotension | targetBased | 339297 | 1446 | 0.549035277361439 | 18 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | ventricular tachycardia | targetBased | 305610 | 1552 | 0.6948342910003 | 133 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | ventricular tachycardia | targetBased | 343666 | 1267 | 0.6948342910003 | 133 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | ventricular tachycardia | targetBased | 342084 | 3260 | 0.6948342910003 | 133 |
Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | HTR2A | ventricular tachycardia | targetBased | 363803 | 2412 | 0.577574040941104 | 8 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Agonists | D2_agonists | ventricular tachycardia | targetBased | 359518 | 300 | 0.577168330395272 | 6 |
HTS Assay for Allosteric Agonists of the Human D2 Dopamine Receptor: Primary Screen for Agonists | D2_agonists | ventricular tachycardia | targetBased | 335652 | 1779 | 0.577168330395272 | 6 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | D2_antagonists | ventricular tachycardia | targetBased | 362274 | 1056 | 0.577168330395272 | 6 |
HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | D2_antagonists | ventricular tachycardia | targetBased | 336308 | 6862 | 0.577168330395272 | 6 |
Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | D2_PAMs | ventricular tachycardia | targetBased | 357537 | 806 | 0.577168330395272 | 6 |
HTS Assay for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Primary Screen for Potentiators | D2_PAMs | ventricular tachycardia | targetBased | 339887 | 1178 | 0.577168330395272 | 6 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | ventricular tachycardia | targetBased | 339297 | 1446 | 0.595189466920042 | 12 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | diastolic blood pressure | targetBased | 86095 | 1442 | 0.451433217156287 | 6 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | diastolic blood pressure | targetBased | 86095 | 1151 | 0.451433217156287 | 6 |
uHTS identification of HIF-2a Inhibitors in a luminesence assay | HIF-2a_inhibitors | diastolic blood pressure | targetBased | 363840 | 2624 | 0.393552178253481 | 9 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | diastolic blood pressure | targetBased | 335531 | 328 | 0.470326091275314 | 14 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | diastolic blood pressure | targetBased | 339674 | 2841 | 0.494806026280812 | 27 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | mean arterial pressure | targetBased | 335531 | 328 | 0.450938883450173 | 8 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | mean arterial pressure | targetBased | 339674 | 2841 | 0.448642022948897 | 12 |
Absorbance-based biochemical primary high throughput screening assay to identify activators of Methionine sulfoxide reductase A (MsrA) | MSRA | diastolic blood pressure | targetBased | 362026 | 1074 | 0.425250264145875 | 23 |
Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) | MSRA | diastolic blood pressure | targetBased | 362577 | 2709 | 0.425250264145875 | 23 |
uHTS for identification of Inhibitors of Mdm2/MdmX interaction in luminescent format. | MDM4 | diastolic blood pressure | targetBased | 331671 | 10022 | 0.343307910677457 | 8 |
Primary qHTS for Inhibitors of ATXN expression | ATXN2_repressors | diastolic blood pressure | targetBased | 358434 | 2554 | 0.298344540355862 | 47 |
qHTS for Inhibitors of Inflammasome Signaling: IL-1-beta AlphaLISA Primary Screen | IL-1b Inflammasome | pericarditis | pathwayBased | 362051 | 17187 | 0.549333638497012 | 69 |
HCS assay for microtubule stabilizers | TUBB | pericarditis | targetBased | 195821 | 1625 | 0.52560928186248 | 6 |
qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | GLP1R | acute myocardial infarction | targetBased | 405130 | 6428 | 0.365976586519998 | 53 |
qHTS of GLP-1 Receptor Agonists | GLP1R agonists | acute myocardial infarction | targetBased | 373462 | 23 | 0.365976586519998 | 53 |
qHTS of GLP-1 Receptor Inverse Agonists: (PAM Mode) (Taking the negative queue for PAMs) | GLP1R PAMs | acute myocardial infarction | targetBased | 405130 | 6428 | 0.365976586519998 | 53 |
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 | acute myocardial infarction | targetBased | 99314 | 335 | 0.427547631514323 | 65 |
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 | acute myocardial infarction | targetBased | 196176 | 782 | 0.427547631514323 | 65 |
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 | acute myocardial infarction | targetBased | 99314 | 390 | 0.427547631514323 | 65 |
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 | acute myocardial infarction | targetBased | 196177 | 811 | 0.427547631514323 | 65 |
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 | acute myocardial infarction | targetBased | 196176 | 670 | 0.427547631514323 | 65 |
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 | acute myocardial infarction | targetBased | 196177 | 519 | 0.427547631514323 | 65 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | acute myocardial infarction | targetBased | 339297 | 1446 | 0.510726398888352 | 17 |
Thrombin 1536 HTS | F2_modulation | acute myocardial infarction | targetBased | 217233 | 557 | 0.496166108771324 | 59 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | heart valve disease | targetBased | 335239 | 801 | 0.443766096667661 | 13 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | heart valve disease | targetBased | 335238 | 390 | 0.443766096667661 | 13 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | ST Elevation Myocardial Infarction | targetBased | 335239 | 801 | 0.28904568668655 | 48 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | ST Elevation Myocardial Infarction | targetBased | 335238 | 390 | 0.28904568668655 | 48 |
Thrombin 1536 HTS | F2_modulation | ST Elevation Myocardial Infarction | targetBased | 217233 | 557 | 0.593802462774375 | 9 |
HCS assay for microtubule stabilizers | TUBB | ST Elevation Myocardial Infarction | targetBased | 195821 | 1625 | 0.539555581875448 | 6 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | cardiac arrest | targetBased | 305610 | 1552 | 0.515630405814729 | 31 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | cardiac arrest | targetBased | 343666 | 1267 | 0.515630405814729 | 31 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | cardiac arrest | targetBased | 342084 | 3260 | 0.515630405814729 | 31 |
Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | AVPR1A_agonists | cardiac arrest | targetBased | 324747 | 813 | 0.529763004236026 | 10 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | cardiac arrest | targetBased | 339297 | 1446 | 0.565626365447611 | 27 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | Agents acting on the renin-angiotensin system use measurement | targetBased | 335531 | 328 | 0.443260371744578 | 6 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | Prinzmetal's angina | targetBased | 335531 | 328 | 0.664977476876164 | 306 |
Screen for inhibitors of the SWI/SNF chromatin remodeling complex (esBAF) in mouse embryonic stem cells with Luciferase reporter assay Measured in Cell-Based System Using Plate Reader - 2141-01_Inhibitor_SinglePoint_HTS_Activity | SMARCA4 | atrial heart septal defect | targetBased | 344733 | 7043 | 0.300714231973763 | 11 |
uHTS identification of small molecule modulators of NR3A | GRIN3A | cerebral atherosclerosis | targetBased | 339772 | 8480 | 0.638992421523723 | 21 |
Thrombin 1536 HTS | F2_modulation | intermediate coronary syndrome | targetBased | 217233 | 557 | 0.543359118242622 | 6 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | Myocardial Ischemia | targetBased | 86095 | 1442 | 0.440369982475793 | 47 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | Myocardial Ischemia | targetBased | 86095 | 1151 | 0.440369982475793 | 47 |
HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | ESR2_inhibitors | Myocardial Ischemia | targetBased | 86095 | 1114 | 0.423950615788154 | 14 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | Myocardial Ischemia | targetBased | 335531 | 328 | 0.574534968426493 | 8 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | Myocardial Ischemia | targetBased | 339297 | 1446 | 0.434244558165963 | 29 |
HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Inhibitor_SinglePoint_HTS_Activity | SCARB1 | Myocardial Ischemia | targetBased | 319204 | 3065 | 0.33411871853546 | 9 |
HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity | SCARB1 | Myocardial Ischemia | targetBased | 316970 | 306 | 0.33411871853546 | 9 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Wolff-Parkinson-White Syndrome | targetBased | 305610 | 3878 | 0.385390364097753 | 8 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Wolff-Parkinson-White Syndrome | targetBased | 305610 | 1082 | 0.385390364097753 | 8 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | systolic heart failure | targetBased | 335239 | 801 | 0.407578504803233 | 8 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | systolic heart failure | targetBased | 335238 | 390 | 0.407578504803233 | 8 |
Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | PLA2G7 | endothelial dysfunction | targetBased | 326024 | 4934 | 0.289018312328131 | 68 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Prolonged QT interval | targetBased | 305610 | 3878 | 0.734109946020632 | 2070 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Prolonged QT interval | targetBased | 305610 | 1082 | 0.734109946020632 | 2070 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Prolonged QT interval | targetBased | 305610 | 1552 | 0.734041769977036 | 3500 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Prolonged QT interval | targetBased | 343666 | 1267 | 0.734041769977036 | 3500 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Prolonged QT interval | targetBased | 342084 | 3260 | 0.734041769977036 | 3500 |
Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 1 (CHRM1) | CHRM1_agonists | Bradycardia | targetBased | 359207 | 1189 | 0.556882803103682 | 6 |
Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | CHRM1_allosteric_activators | Bradycardia | targetBased | 63676 | 1938 | 0.556882803103682 | 6 |
Fluorescence-based cell-based primary high throughput screening assay to identify positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1). | CHRM1_PAMs | Bradycardia | targetBased | 359207 | 316 | 0.556882803103682 | 6 |
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | CHRM1_allosteric_antagonists | Bradycardia | targetBased | 63656 | 2179 | 0.556882803103682 | 6 |
Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | CHRM1_antgonists | Bradycardia | targetBased | 359207 | 4555 | 0.556882803103682 | 6 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | Bradycardia | targetBased | 339297 | 1446 | 0.507645320472039 | 6 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Ventricular fibrillation | targetBased | 305610 | 1552 | 0.407152792746921 | 42 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Ventricular fibrillation | targetBased | 343666 | 1267 | 0.407152792746921 | 42 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Ventricular fibrillation | targetBased | 342084 | 3260 | 0.407152792746921 | 42 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Abnormality of the cardiovascular system | targetBased | 305610 | 3878 | 0.675190267140752 | 1550 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Abnormality of the cardiovascular system | targetBased | 305610 | 1082 | 0.675190267140752 | 1550 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Abnormality of the cardiovascular system | targetBased | 305610 | 1552 | 0.711592736821994 | 2381 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Abnormality of the cardiovascular system | targetBased | 343666 | 1267 | 0.711592736821994 | 2381 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Abnormality of the cardiovascular system | targetBased | 342084 | 3260 | 0.711592736821994 | 2381 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | Abnormality of the cardiovascular system | pathwayBased | 70898 | 707 | 0.481626628052691 | 19 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | Abnormality of the cardiovascular system | pathwayBased | 131324 | 544 | 0.481626628052691 | 19 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | Abnormality of the cardiovascular system | targetBased | 305610 | 2592 | 0.612683747155337 | 239 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | Abnormality of the cardiovascular system | targetBased | 335239 | 801 | 0.630409551474951 | 502 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | Abnormality of the cardiovascular system | targetBased | 335238 | 390 | 0.630409551474951 | 502 |
HTS of Smad transcription factor inhibitors | SMAD3 | Abnormality of the cardiovascular system | targetBased | 88033 | 251 | 0.406522914717714 | 73 |
qHTS Assay for Activators of Human alpha-Glucosidase as a Potential Chaperone Treatment of Pompe Disease | GAA | Abnormality of the cardiovascular system | targetBased | 199169 | 715 | 0.569277510327076 | 411 |
qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | GAA_inhibitors | Abnormality of the cardiovascular system | targetBased | 302297 | 1165 | 0.569277510327076 | 411 |
HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | HRAS | Abnormality of the cardiovascular system | targetBased | 194628 | 267 | 0.536386687475283 | 104 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | Abnormal heart morphology | pathwayBased | 70898 | 707 | 0.53214174757145 | 9 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | Abnormal heart morphology | pathwayBased | 131324 | 544 | 0.53214174757145 | 9 |
HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | TRPV1 | Patent ductus arteriosus | targetBased | 316642 | 617 | 0.567131293854564 | 20 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | Ischemic stroke | targetBased | 335531 | 328 | 0.516525873530802 | 9 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | Ischemic stroke | targetBased | 339297 | 1446 | 0.436685419032319 | 8 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn6) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | Ischemic stroke | targetBased | 369953 | 760 | 0.312229359586519 | 12 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn7) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | Ischemic stroke | targetBased | 369953 | 498 | 0.312229359586519 | 12 |
Thrombin 1536 HTS | F2_modulation | Ischemic stroke | targetBased | 217233 | 557 | 0.353397775729454 | 20 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Ventricular arrhythmia | targetBased | 305610 | 1552 | 0.683101878753051 | 162 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Ventricular arrhythmia | targetBased | 343666 | 1267 | 0.683101878753051 | 162 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Ventricular arrhythmia | targetBased | 342084 | 3260 | 0.683101878753051 | 162 |
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 | Ventricular arrhythmia | targetBased | 335239 | 991 | 0.439916790832495 | 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 | Ventricular arrhythmia | targetBased | 335239 | 695 | 0.439916790832495 | 8 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | Ventricular arrhythmia | targetBased | 339297 | 1446 | 0.641084137971574 | 32 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | Reduced left ventricular ejection fraction | targetBased | 335531 | 328 | 0.563971467918354 | 9 |
HTS of Smad transcription factor inhibitors | SMAD3 | Vascular dilatation | targetBased | 88033 | 251 | 0.293136199956077 | 7 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Arrhythmia | targetBased | 305610 | 1552 | 0.260133066682535 | 69 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Arrhythmia | targetBased | 343666 | 1267 | 0.260133066682535 | 69 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Arrhythmia | targetBased | 342084 | 3260 | 0.260133066682535 | 69 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | heart conduction disease | targetBased | 305610 | 2592 | 0.271846747382295 | 290 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | short QT syndrome | targetBased | 305610 | 3878 | 0.568605630843682 | 215 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | short QT syndrome | targetBased | 305610 | 1082 | 0.568605630843682 | 215 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | short QT syndrome | targetBased | 305610 | 1552 | 0.41039245993415 | 99 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | short QT syndrome | targetBased | 343666 | 1267 | 0.41039245993415 | 99 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | short QT syndrome | targetBased | 342084 | 3260 | 0.41039245993415 | 99 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | short QT syndrome | targetBased | 305610 | 2592 | 0.443689779602828 | 318 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | essential hypertension | targetBased | 335531 | 328 | 0.655030426761749 | 86 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | essential hypertension | targetBased | 339297 | 1446 | 0.306714129819747 | 10 |
uHTS Luminescent assay for identification of inhibitors of NALP3 in yeast | NLRP3 | pericardial effusion | targetBased | 330392 | 1295 | 0.284879239032575 | 8 |
High Throughput Screening for Cocaine Antagonists: Primary Screen | SLC6A3 | arteriosclerosis disorder | targetBased | 108286 | 1415 | 0.552064990371929 | 6 |
HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | ESR1_inhibitors | thrombotic disease | targetBased | 86095 | 1442 | 0.286083808767426 | 13 |
HTS of Estrogen Receptor- alpha Coactivator Binding Potentiators | ESR1_modulators | thrombotic disease | targetBased | 86095 | 1151 | 0.286083808767426 | 13 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn6) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | thrombotic disease | targetBased | 369953 | 760 | 0.514268280638907 | 18 |
Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn7) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | FGB_inhibitors | thrombotic disease | targetBased | 369953 | 498 | 0.514268280638907 | 18 |
Thrombin 1536 HTS | F2_modulation | thrombotic disease | targetBased | 217233 | 557 | 0.629548975281352 | 445 |
Screen for inhibitors of the SWI/SNF chromatin remodeling complex (esBAF) in mouse embryonic stem cells with Luciferase reporter assay Measured in Cell-Based System Using Plate Reader - 2141-01_Inhibitor_SinglePoint_HTS_Activity | SMARCA4 | ventricular septal defect | targetBased | 344733 | 7043 | 0.293378171058506 | 11 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Jervell and Lange-Nielsen syndrome | targetBased | 305610 | 3878 | 0.829758025318848 | 193 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Jervell and Lange-Nielsen syndrome | targetBased | 305610 | 1082 | 0.829758025318848 | 193 |
Nrf2 qHTS screen for inhibitors | nrf2Inhibitors | pulmonary hypertension | targetBased | 360873 | 7438 | 0.295826525946821 | 9 |
qHTS of Nrf2 Activators | Nrf2 activators | pulmonary hypertension | pathwayBased | 403871 | 1243 | 0.295826525946821 | 9 |
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 | pulmonary hypertension | targetBased | 99314 | 335 | 0.307468927254904 | 180 |
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 | pulmonary hypertension | targetBased | 196176 | 782 | 0.307468927254904 | 180 |
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 | pulmonary hypertension | targetBased | 99314 | 390 | 0.307468927254904 | 180 |
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 | pulmonary hypertension | targetBased | 196177 | 811 | 0.307468927254904 | 180 |
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 | pulmonary hypertension | targetBased | 196176 | 670 | 0.307468927254904 | 180 |
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 | pulmonary hypertension | targetBased | 196177 | 519 | 0.307468927254904 | 180 |
Natriuretic polypeptide receptor (hNpr1) antagonism - Primary qHTS | NPR1 | pulmonary hypertension | targetBased | 76168 | 1231 | 0.514121558566674 | 17 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | pulmonary hypertension | targetBased | 339674 | 2841 | 0.293303559901386 | 183 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | sinoatrial node dysfunction and deafness | targetBased | 335531 | 328 | 0.798234352836398 | 89 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Brugada syndrome | targetBased | 305610 | 3878 | 0.399136095092878 | 52 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Brugada syndrome | targetBased | 305610 | 1082 | 0.399136095092878 | 52 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Brugada syndrome | targetBased | 305610 | 1552 | 0.478699522092586 | 53 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Brugada syndrome | targetBased | 343666 | 1267 | 0.478699522092586 | 53 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Brugada syndrome | targetBased | 342084 | 3260 | 0.478699522092586 | 53 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | familial atrial fibrillation | targetBased | 305610 | 3878 | 0.584915503283993 | 198 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | familial atrial fibrillation | targetBased | 305610 | 1082 | 0.584915503283993 | 198 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | familial atrial fibrillation | targetBased | 305610 | 2592 | 0.557484038987195 | 108 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | familial long QT syndrome | targetBased | 305610 | 3878 | 0.858261017924304 | 1652 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | familial long QT syndrome | targetBased | 305610 | 1082 | 0.858261017924304 | 1652 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | familial long QT syndrome | targetBased | 305610 | 1552 | 0.810413609236612 | 888 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | familial long QT syndrome | targetBased | 343666 | 1267 | 0.810413609236612 | 888 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | familial long QT syndrome | targetBased | 342084 | 3260 | 0.810413609236612 | 888 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | familial long QT syndrome | targetBased | 305610 | 2592 | 0.399973484574095 | 407 |
HTS of Smad transcription factor inhibitors | SMAD3 | familial thoracic aortic aneurysm and aortic dissection | targetBased | 88033 | 251 | 0.777860473513668 | 1211 |
HTS for Beta-2AR agonists via FAP method | ADRB2_activators | coronary atherosclerosis | targetBased | 339297 | 1446 | 0.577168330395272 | 6 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Romano-Ward syndrome | targetBased | 305610 | 3878 | 0.917575767779804 | 689 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Romano-Ward syndrome | targetBased | 305610 | 1082 | 0.917575767779804 | 689 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Romano-Ward syndrome | targetBased | 305610 | 1552 | 0.93814629135582 | 1206 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Romano-Ward syndrome | targetBased | 343666 | 1267 | 0.93814629135582 | 1206 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Romano-Ward syndrome | targetBased | 342084 | 3260 | 0.93814629135582 | 1206 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Familial progressive cardiac conduction defect | targetBased | 305610 | 3878 | 0.425086943408605 | 8 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Familial progressive cardiac conduction defect | targetBased | 305610 | 1082 | 0.425086943408605 | 8 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Familial short QT syndrome | targetBased | 305610 | 3878 | 0.764568393200508 | 60 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Familial short QT syndrome | targetBased | 305610 | 1082 | 0.764568393200508 | 60 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Familial short QT syndrome | targetBased | 305610 | 1552 | 0.828402105198518 | 351 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Familial short QT syndrome | targetBased | 343666 | 1267 | 0.828402105198518 | 351 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Familial short QT syndrome | targetBased | 342084 | 3260 | 0.828402105198518 | 351 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | Familial short QT syndrome | targetBased | 305610 | 2592 | 0.699555539533156 | 30 |
Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | Rare familial disorder with hypertrophic cardiomyopathy | targetBased | 335239 | 801 | 0.622584838782076 | 123 |
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | TNNI3 | Rare familial disorder with hypertrophic cardiomyopathy | targetBased | 335238 | 390 | 0.622584838782076 | 123 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | MAPK1 | heart disease | pathwayBased | 70898 | 707 | 0.267588911577723 | 55 |
qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | MAPK1 | heart disease | pathwayBased | 131324 | 544 | 0.267588911577723 | 55 |
Primary Cell-based High Throughput Screening assay for activators of the nuclear receptor Steroidogenic Factor 1 (SF-1) | NR5A1 | heart disease | targetBased | 64908 | 1225 | 0.295511338182346 | 54 |
Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | NR5A1 | heart disease | targetBased | 64908 | 359 | 0.295511338182346 | 54 |
HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | HRAS | heart disease | targetBased | 194628 | 267 | 0.324902614329253 | 459 |
Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of COUP-TFII (NR2F2) | NR2F2 | heart disease | targetBased | 369953 | 2602 | 0.266850434050765 | 68 |
Factor XIa 1536 HTS | F11_modulation | vascular disease | targetBased | 218707 | 302 | 0.261925524783603 | 92 |
Factor XIIa 1536 HTS | F12_modulation | vascular disease | targetBased | 217430 | 649 | 0.29737794501814 | 65 |
HTS identification of compounds activating phosphomannose isomerase (PMI) via a fluorescence intensity assay using a near- saturating concentration of mannose 6-phosphat | MPI | vascular disease | targetBased | 194152 | 656 | 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 | vascular disease | targetBased | 194152 | 1288 | 0.307418870150215 | 258 |
HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | MPI | vascular disease | targetBased | 194152 | 814 | 0.307418870150215 | 258 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | congenital heart disease | targetBased | 305610 | 3878 | 0.32583345778383 | 977 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | congenital heart disease | targetBased | 305610 | 1082 | 0.32583345778383 | 977 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | congenital heart disease | targetBased | 305610 | 2592 | 0.309305482466369 | 384 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Abnormal cardiovascular system physiology | targetBased | 305610 | 3878 | 0.255900041100298 | 715 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Abnormal cardiovascular system physiology | targetBased | 305610 | 1082 | 0.255900041100298 | 715 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Abnormal cardiovascular system physiology | targetBased | 305610 | 1552 | 0.292071884654771 | 1238 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Abnormal cardiovascular system physiology | targetBased | 343666 | 1267 | 0.292071884654771 | 1238 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Abnormal cardiovascular system physiology | targetBased | 342084 | 3260 | 0.292071884654771 | 1238 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Abnormality of cardiovascular system electrophysiology | targetBased | 305610 | 1552 | 0.291052991639106 | 1235 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Abnormality of cardiovascular system electrophysiology | targetBased | 343666 | 1267 | 0.291052991639106 | 1235 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Abnormality of cardiovascular system electrophysiology | targetBased | 342084 | 3260 | 0.291052991639106 | 1235 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | arterial disorder | targetBased | 335531 | 328 | 0.263043575919809 | 683 |
Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK3 | KCNK3 | arterial disorder | targetBased | 339674 | 2841 | 0.307605371317295 | 175 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | heart conduction disease | targetBased | 305610 | 3878 | 0.27147277959172 | 184 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | heart conduction disease | targetBased | 305610 | 1082 | 0.27147277959172 | 184 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | cardiac rhythm disease | targetBased | 305610 | 3878 | 0.278174095876582 | 223 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | cardiac rhythm disease | targetBased | 305610 | 1082 | 0.278174095876582 | 223 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | cardiac rhythm disease | targetBased | 305610 | 1552 | 0.280032584227586 | 211 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | cardiac rhythm disease | targetBased | 343666 | 1267 | 0.280032584227586 | 211 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | cardiac rhythm disease | targetBased | 342084 | 3260 | 0.280032584227586 | 211 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | cardiac rhythm disease | targetBased | 305610 | 2592 | 0.297439427831753 | 156 |
HTS for Inhibition of CaV1.3 ICDI/IQ interaction using a live-cell FRET assay Measured in Cell-Based System Using Plate Reader - 7081-01_Inhibitor_SinglePoint_HTS_Activity | CACNA1D_inhibitors | cardiac rhythm disease | targetBased | 335531 | 328 | 0.304830752442955 | 74 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | congenital anomaly of cardiovascular system | targetBased | 305610 | 3878 | 0.32583345778383 | 977 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | congenital anomaly of cardiovascular system | targetBased | 305610 | 1082 | 0.32583345778383 | 977 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | congenital anomaly of cardiovascular system | targetBased | 305610 | 1552 | 0.270770606427675 | 331 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | congenital anomaly of cardiovascular system | targetBased | 343666 | 1267 | 0.270770606427675 | 331 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | congenital anomaly of cardiovascular system | targetBased | 342084 | 3260 | 0.270770606427675 | 331 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | congenital anomaly of cardiovascular system | targetBased | 305610 | 2592 | 0.309305482466369 | 384 |
Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of COUP-TFII (NR2F2) | NR2F2 | congenital anomaly of cardiovascular system | targetBased | 369953 | 2602 | 0.266500325775173 | 60 |
qHTS Assay for Activators of Human alpha-Glucosidase as a Potential Chaperone Treatment of Pompe Disease | GAA | Glycogen storage disease with hypertrophic cardiomyopathy | targetBased | 199169 | 715 | 0.305413139539117 | 1578 |
qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | GAA_inhibitors | Glycogen storage disease with hypertrophic cardiomyopathy | targetBased | 302297 | 1165 | 0.305413139539117 | 1578 |
qHTS Assay for Activators of Human alpha-Glucosidase as a Potential Chaperone Treatment of Pompe Disease | GAA | Lysosomal disease with hypertrophic cardiomyopathy | targetBased | 199169 | 715 | 0.305413139539117 | 1578 |
qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | GAA_inhibitors | Lysosomal disease with hypertrophic cardiomyopathy | targetBased | 302297 | 1165 | 0.305413139539117 | 1578 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | KCNQ1 | Rare genetic cardiac disease | targetBased | 305610 | 3878 | 0.314483144382057 | 259 |
Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | KCNQ1 | Rare genetic cardiac disease | targetBased | 305610 | 1082 | 0.314483144382057 | 259 |
Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | KCNH2 | Rare genetic cardiac disease | targetBased | 305610 | 1552 | 0.319539417013411 | 532 |
qHTS for Inhibitors of KCHN2 3.1: Wildtype qHTS | KCNH2 | Rare genetic cardiac disease | targetBased | 343666 | 1267 | 0.319539417013411 | 532 |
qHTS for Inhibitors of KCHN2 3.1: Mutant qHTS | KCNH2 | Rare genetic cardiac disease | targetBased | 342084 | 3260 | 0.319539417013411 | 532 |
Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | KCNJ2 | Rare genetic cardiac disease | targetBased | 305610 | 2592 | 0.304986033813229 | 316 |
qHTS Assay for Activators of Human alpha-Glucosidase as a Potential Chaperone Treatment of Pompe Disease | GAA | Rare genetic cardiac disease | targetBased | 199169 | 715 | 0.305534076087638 | 1590 |
qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | GAA_inhibitors | Rare genetic cardiac disease | targetBased | 302297 | 1165 | 0.305534076087638 | 1590 |
qHTS Assay for Activators of Human alpha-Glucosidase as a Potential Chaperone Treatment of Pompe Disease | GAA | Rare familial disorder with hypertrophic cardiomyopathy | targetBased | 199169 | 715 | 0.305428913809152 | 1579 |
qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | GAA_inhibitors | Rare familial disorder with hypertrophic cardiomyopathy | targetBased | 302297 | 1165 | 0.305428913809152 | 1579 |
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