| 1 | [SID14743393] | Active | EC50 | 0.596 | Confirmation dose response assay for compounds that activate transient receptor potential cation channel C4 (TRPC4) [AID434937, Type: confirmatory] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | EC50 | 0.596 [uM] | | BioAssay | Confirmation dose response assay for compounds that activate transient receptor potential cation channel C4 (TRPC4) | | AID | 434937 | | BioAssay type | confirmatory | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
|
| 2 | [SID14743393] | Active | Potency | 2.8184 | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) [AID651820, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 2.8184 [uM] | | BioAssay | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) | | AID | 651820 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 3 | [SID87348216] | Active | EC50 | 2.953 | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID588407, Type: confirmatory] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | EC50 | 2.953 [uM] | | BioAssay | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 588407 | | BioAssay type | confirmatory | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 4 | [SID87348216] | Active | EC50 | 2.953 | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID588407, Type: confirmatory] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | EC50 | 2.953 [uM] | | BioAssay | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 588407 | | BioAssay type | confirmatory | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 5 | [SID87348216] | Active | EC50 | 3.961 | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRD1 homodimerization [AID588411, Type: confirmatory] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | EC50 | 3.961 [uM] | | BioAssay | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRD1 homodimerization | | AID | 588411 | | BioAssay type | confirmatory | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 6 | [SID87348216] | Active | EC50 | 3.961 | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRD1 homodimerization [AID588411, Type: confirmatory] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | EC50 | 3.961 [uM] | | BioAssay | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRD1 homodimerization | | AID | 588411 | | BioAssay type | confirmatory | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 7 | [SID14743393] | Active | Potency | 8.2753 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 8.2753 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | | AID | 504834 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 8 | [SID14743393] | Active | Potency | 10 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line [AID686971, Type: confirmatory] | |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line | | AID | 686971 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 9 | [SID14743393] | Active | Potency | 11.2202 | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2551 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 10 | [SID14743393] | Active | Potency | 12.9953 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 12.9953 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 11 | [SID14743393] | Active | Potency | 12.9953 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 12.9953 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 12 | [SID14743393] | Active | Potency | 12.9953 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 12.9953 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 13 | [SID14743393] | Active | Potency | 20.5962 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 20.5962 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 14 | [SID14743393] | Active | Potency | 20.5962 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 20.5962 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 15 | [SID14743393] | Active | Potency | 20.5962 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | Potency | 20.5962 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 16 | [SID87348216] | Active | IC50 | 27.3 | Dose response confirmation of uHTS RPN11 inhibitor hits in a Fluorescence Polarization assay [AID602368, Type: confirmatory] | PSMD14 protein [Homo sapiens] [gi:16306916] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | IC50 | 27.3 [uM] | | BioAssay | Dose response confirmation of uHTS RPN11 inhibitor hits in a Fluorescence Polarization assay | | AID | 602368 | | BioAssay type | confirmatory | | Target | PSMD14 protein [Homo sapiens] [gi:16306916] | | PubMed | | | Data Table |  |
|
| 17 | [SID87348216] | Active | IC50 | 97.7 | Dose Response validation of uHTS RPN11 inhibitor hits using a Thrombin Fluorescence Polarization assay [AID602369, Type: confirmatory] | prothrombin [Bos taurus] [gi:296479639] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | IC50 | 97.7 [uM] | | BioAssay | Dose Response validation of uHTS RPN11 inhibitor hits using a Thrombin Fluorescence Polarization assay | | AID | 602369 | | BioAssay type | confirmatory | | Target | prothrombin [Bos taurus] [gi:296479639] | | PubMed | | | Data Table |  |
|
| 18 | [SID87348216] | Active | IC50 | 97.7 | Dose Response validation of uHTS RPN11 inhibitor hits using a Thrombin Fluorescence Polarization assay [AID602369, Type: confirmatory] | prothrombin [Bos taurus] [gi:296479639] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | IC50 | 97.7 [uM] | | BioAssay | Dose Response validation of uHTS RPN11 inhibitor hits using a Thrombin Fluorescence Polarization assay | | AID | 602369 | | BioAssay type | confirmatory | | Target | prothrombin [Bos taurus] [gi:296479639] | | PubMed | | | Data Table |  |
|
| 19 | [SID14743393] | Active | | | Specificity screen against TRPC6 for compounds that activate transient receptor potential cation channel C4 (TRPC4) [AID434950, Type: screening] | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Specificity screen against TRPC6 for compounds that activate transient receptor potential cation channel C4 (TRPC4) | | AID | 434950 | | BioAssay type | screening | | Target | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] | | PubMed | | | Data Table |  |
|
| 20 | [SID87348216] | Active | | | uHTS identification of inhibitors of Rpn11 in a Fluorescent Polarization assay [AID588493, Type: screening] | PSMD14 protein [Homo sapiens] [gi:16306916] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | BioAssay | uHTS identification of inhibitors of Rpn11 in a Fluorescent Polarization assay | | AID | 588493 | | BioAssay type | screening | | Target | PSMD14 protein [Homo sapiens] [gi:16306916] | | PubMed | | | Data Table |  |
|
| 21 | [SID14743393] | Active | | | Confirmatory screen for identification of compounds that activate transient receptor potential cation channel C4 (TRPC4) [AID2426, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Confirmatory screen for identification of compounds that activate transient receptor potential cation channel C4 (TRPC4) | | AID | 2426 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
|
| 22 | [SID14743393] | Active | | | Confirmatory screen for identification of compounds that inhibit transient receptor potential cation channel C6 (TRPC6) [AID488960, Type: screening] | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Confirmatory screen for identification of compounds that inhibit transient receptor potential cation channel C6 (TRPC6) | | AID | 488960 | | BioAssay type | screening | | Target | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] | | PubMed | | | Data Table |  |
|
| 23 | [SID87348216] | Active | | | Single concentration confirmation of uHTS inhibitor hits from RPN11 in a Fluorescence Polarization assay [AID602318, Type: screening] | PSMD14 protein [Homo sapiens] [gi:16306916] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS inhibitor hits from RPN11 in a Fluorescence Polarization assay | | AID | 602318 | | BioAssay type | screening | | Target | PSMD14 protein [Homo sapiens] [gi:16306916] | | PubMed | | | Data Table |  |
|
| 24 | [SID14743393] | Active | | | Primary cell-based high throughput screening assay to measure STAT3 activation [AID871, Type: screening] | STAT3 [Homo sapiens] [gi:13272532] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT3 activation | | AID | 871 | | BioAssay type | screening | | Target | STAT3 [Homo sapiens] [gi:13272532] | | PubMed | | | Data Table |  |
|
| 25 | [SID14743393] | Active | | | Primary cell-based high throughput screening assay to measure STAT3 activation [AID871, Type: screening] | STAT3 [Homo sapiens] [gi:13272532] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT3 activation | | AID | 871 | | BioAssay type | screening | | Target | STAT3 [Homo sapiens] [gi:13272532] | | PubMed | | | Data Table |  |
|
| 26 | [SID14743393] | Active | | | Primary cell-based high throughput screening assay to measure STAT3 activation [AID871, Type: screening] | STAT3 [Homo sapiens] [gi:13272532] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT3 activation | | AID | 871 | | BioAssay type | screening | | Target | STAT3 [Homo sapiens] [gi:13272532] | | PubMed | | | Data Table |  |
|
| 27 | [SID14743393] | Active | | | Specificity screen against KCNQ2 for identification of compounds that inhibit KCNQ1 potassium channels [AID651746, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Specificity screen against KCNQ2 for identification of compounds that inhibit KCNQ1 potassium channels | | AID | 651746 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 28 | [SID14743393] | Active | | | Specificity screen against KCNQ2 for identification of compounds that inhibit KCNQ1 potassium channels [AID651746, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Specificity screen against KCNQ2 for identification of compounds that inhibit KCNQ1 potassium channels | | AID | 651746 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 29 | [SID14743393] | Active | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
|
| 30 | [SID14743393] | Active | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
|
| 31 | [SID14743393] | Active | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
|
| 32 | [SID14743393] | Active | | | Second specificity screen against TRPC4 for compounds that inhibit transient receptor potential cation channel C6 (TRPC6) [AID2776, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Second specificity screen against TRPC4 for compounds that inhibit transient receptor potential cation channel C6 (TRPC6) | | AID | 2776 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
|
| 33 | [SID14743393] | Active | | | Specificity screen against TRPC4 for compounds that inhibit transient receptor potential cation channel C6 (TRPC6) [AID2777, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Specificity screen against TRPC4 for compounds that inhibit transient receptor potential cation channel C6 (TRPC6) | | AID | 2777 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
|
| 34 | [SID14743393] | Active | | | Primary cell-based screen for identification of compounds that activate transient receptor potential cation channel C4 (TRPC4). [AID2237, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Primary cell-based screen for identification of compounds that activate transient receptor potential cation channel C4 (TRPC4). | | AID | 2237 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
|
| 35 | [SID14743393] | Active | | | Second counter screen for compounds that activate transient receptor potential cation channel C4 (TRPC4). [AID434977, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Second counter screen for compounds that activate transient receptor potential cation channel C4 (TRPC4). | | AID | 434977 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
|
| 36 | [SID14743393] | Active | | | Validation (re-confirmation) assay for identification of compounds that inhibit KCNQ1 potassium channels [AID588353, Type: screening] | KCNQ1 gene product [Homo sapiens] [gi:32479527] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Validation (re-confirmation) assay for identification of compounds that inhibit KCNQ1 potassium channels | | AID | 588353 | | BioAssay type | screening | | Target | KCNQ1 gene product [Homo sapiens] [gi:32479527] | | PubMed | | | Data Table |  |
|
| 37 | [SID87348216] | Active | | | 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 [AID504326, Type: screening] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | BioAssay | 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 | | AID | 504326 | | BioAssay type | screening | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 38 | [SID87348216] | Active | | | 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 [AID504326, Type: screening] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | BioAssay | 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 | | AID | 504326 | | BioAssay type | screening | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 39 | [SID87348216] | Active | | | Luminescence-based cell-based high throughput confirmation assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID504904, Type: screening] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | BioAssay | Luminescence-based cell-based high throughput confirmation assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 504904 | | BioAssay type | screening | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 40 | [SID87348216] | Active | | | Luminescence-based cell-based high throughput confirmation assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID504904, Type: screening] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 87348216 | | CID | 2037119 | | Outcome | Active | | BioAssay | Luminescence-based cell-based high throughput confirmation assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 504904 | | BioAssay type | screening | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 41 | [SID14743393] | Active | | | High throughput screening of inhibitors of transient receptor potential cation channel C6 (TRPC6) [AID2553, Type: screening] | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | High throughput screening of inhibitors of transient receptor potential cation channel C6 (TRPC6) | | AID | 2553 | | BioAssay type | screening | | Target | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] | | PubMed | | | Data Table |  |
|
| 42 | [SID14743393] | Active | | | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. [AID1381, Type: screening] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. | | AID | 1381 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 43 | [SID14743393] | Active | | | Leishmania major promastigote HTS [AID1063, Type: screening] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Leishmania major promastigote HTS | | AID | 1063 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 44 | [SID14743393] | Active | | | Counter screen for compounds that inhibit transient receptor potential cation channel C6 (TRPC6) [AID2780, Type: screening] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Counter screen for compounds that inhibit transient receptor potential cation channel C6 (TRPC6) | | AID | 2780 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 45 | [SID14743393] | Active | | | Antagonist of Human D 1 Dopamine Receptor: qHTS [AID504652, Type: screening] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Antagonist of Human D 1 Dopamine Receptor: qHTS | | AID | 504652 | | BioAssay type | screening | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 46 | [SID14743393] | Active | | | Antagonist of Human D 1 Dopamine Receptor: qHTS [AID504652, Type: screening] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Antagonist of Human D 1 Dopamine Receptor: qHTS | | AID | 504652 | | BioAssay type | screening | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 47 | [SID14743393] | Active | | | Antagonist of Human D 1 Dopamine Receptor: qHTS [AID504652, Type: screening] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Antagonist of Human D 1 Dopamine Receptor: qHTS | | AID | 504652 | | BioAssay type | screening | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 48 | [SID14743393] | Active | | | Antagonist of Human D 1 Dopamine Receptor: qHTS [AID504652, Type: screening] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Antagonist of Human D 1 Dopamine Receptor: qHTS | | AID | 504652 | | BioAssay type | screening | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 49 | [SID14743393] | Active | | | Activators of the GIRK family of Potassium Channels (GIRK1/2_Confirmatory) [AID623911, Type: other] | G protein-activated inward rectifier potassium channel 1 [gi:1352482] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Activators of the GIRK family of Potassium Channels (GIRK1/2_Confirmatory) | | AID | 623911 | | BioAssay type | other | | Target | G protein-activated inward rectifier potassium channel 1 [gi:1352482] | | PubMed | | | Data Table |  |
|
| 50 | [SID14743393] | Active | | | Activators of the GIRK family of Potassium Channels (GIRK1/2_Confirmatory) [AID623911, Type: other] | G protein-activated inward rectifier potassium channel 1 [gi:1352482] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 14743393 | | CID | 2037119 | | Outcome | Active | | BioAssay | Activators of the GIRK family of Potassium Channels (GIRK1/2_Confirmatory) | | AID | 623911 | | BioAssay type | other | | Target | G protein-activated inward rectifier potassium channel 1 [gi:1352482] | | PubMed | | | Data Table |  |
|