| 1 | [SID7970631] | Chemical Probe | | | Summary of probe development efforts to identify inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1). [AID1844, Type: summary] | steroidogenic factor-1 [Homo sapiens] [gi:216409744] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Chemical Probe | | BioAssay | Summary of probe development efforts to identify inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1). | | AID | 1844 | | BioAssay type | summary | | Target | steroidogenic factor-1 [Homo sapiens] [gi:216409744] | | PubMed | | | Data Table |  |
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| 2 | [SID7970631] | Chemical Probe | | | Summary of probe development efforts to identify inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1). [AID1844, Type: summary] | steroidogenic factor-1 [Homo sapiens] [gi:216409744] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Chemical Probe | | BioAssay | Summary of probe development efforts to identify inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1). | | AID | 1844 | | BioAssay type | summary | | Target | steroidogenic factor-1 [Homo sapiens] [gi:216409744] | | PubMed | | | Data Table |  |
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| 3 | [SID7970631] | Chemical Probe | | | Summary of probe development efforts to identify inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1). [AID1844, Type: summary] | steroidogenic factor-1 [Homo sapiens] [gi:216409744] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Chemical Probe | | BioAssay | Summary of probe development efforts to identify inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1). | | AID | 1844 | | BioAssay type | summary | | Target | steroidogenic factor-1 [Homo sapiens] [gi:216409744] | | PubMed | | | Data Table |  |
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| 4 | [SID103565234] | Active | IC50 | 0.26 | Inhibition of GAL4-tagged NR5A1 by luciferase assay [AID329653, Type: Literature] | |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103565234 | | CID | 4289057 | | Outcome | Active | | IC50 | 0.26 [uM] | | BioAssay | Inhibition of GAL4-tagged NR5A1 by luciferase assay | | AID | 329653 | | BioAssay type | Literature | | Target | | | PubMed | 18374567 | | Data Table |  |
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| 5 | [SID7970631] | Active | IC50 | 2.23 | Dose response counterscreen of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a HEK-293T cell line using a luminescence assay [AID489041, Type: confirmatory] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | IC50 | 2.23 [uM] | | BioAssay | Dose response counterscreen of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a HEK-293T cell line using a luminescence assay | | AID | 489041 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 6 | [SID7970631] | Active | Potency | 2.3109 | 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. | 6 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 2.3109 [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 |  |
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| 7 | [SID7970631] | Active | Potency | 2.3109 | 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. | 7 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 2.3109 [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 |  |
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| 8 | [SID7970631] | Active | Potency | 2.3109 | 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. | 8 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 2.3109 [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 |  |
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| 9 | [SID7970631] | Active | Potency | 2.5929 | 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. | 9 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 2.5929 [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 |  |
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| 10 | [SID7970631] | Active | Potency | 2.5929 | 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 | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 2.5929 [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 |  |
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| 11 | [SID7970631] | Active | Potency | 2.5929 | 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 | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 2.5929 [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 |  |
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| 12 | [SID7970631] | Active | Potency | 4.1095 | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. [AID624297, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 4.1095 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. | | AID | 624297 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
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| 13 | [SID56373597] | Active | IC50 | 4.9336 | Confirmation of image-based Screening Assay for Inhibitors of Phagocytosis [AID1618, Type: confirmatory] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 56373597 | | CID | 4289057 | | Outcome | Active | | IC50 | 4.9336 [uM] | | BioAssay | Confirmation of image-based Screening Assay for Inhibitors of Phagocytosis | | AID | 1618 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 14 | [SID7970631] | Active | Potency | 6.5131 | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. [AID624296, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 6.5131 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. | | AID | 624296 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
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| 15 | [SID7970631] | Active | IC50 | 9.88 | Dose response confirmation of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a Jurkat cell line using a luminescence assay [AID489035, Type: confirmatory] | |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | IC50 | 9.88 [uM] | | BioAssay | Dose response confirmation of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a Jurkat cell line using a luminescence assay | | AID | 489035 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 16 | [SID56373597] | Active | IC50 | 11.4 | SAR analysis of compounds that inhibit HePTP - Set 2 [AID449736, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 56373597 | | CID | 4289057 | | Outcome | Active | | IC50 | 11.4 [uM] | | BioAssay | SAR analysis of compounds that inhibit HePTP - Set 2 | | AID | 449736 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 17 | [SID56373597] | Active | IC50 | 11.4 | SAR analysis of compounds that inhibit HePTP - Set 2 [AID449736, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 56373597 | | CID | 4289057 | | Outcome | Active | | IC50 | 11.4 [uM] | | BioAssay | SAR analysis of compounds that inhibit HePTP - Set 2 | | AID | 449736 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 18 | [SID56373597] | Active | IC50 | 11.4 | SAR analysis of compounds that inhibit HePTP - Set 2 [AID449736, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 56373597 | | CID | 4289057 | | Outcome | Active | | IC50 | 11.4 [uM] | | BioAssay | SAR analysis of compounds that inhibit HePTP - Set 2 | | AID | 449736 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 19 | [SID7970631] | Active | Potency | 20.5962 | qHTS Assay to Find Inhibitors of Chronic Active B-Cell Receptor Signaling: Hit Validation in Primary Screen [AID651558, Type: confirmatory] | |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | Potency | 20.5962 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Chronic Active B-Cell Receptor Signaling: Hit Validation in Primary Screen | | AID | 651558 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 20 | [SID7970631] | Active | | | Single concentration confirmation of inhibitors of Mdm2/MdmX interaction using a Full-Length Luciferase Counterscreen assay [AID504607, Type: screening] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Mdm2/MdmX interaction using a Full-Length Luciferase Counterscreen assay | | AID | 504607 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 21 | [SID7970631] | Active | | | Single concentration confirmation of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation [AID435020, Type: screening] | |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Single concentration confirmation of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation | | AID | 435020 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 22 | [SID7970631] | Active | | | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation [AID435003, Type: screening] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation | | AID | 435003 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 23 | [SID7970631] | Active | | | Human H69AR Lung Tumor Cell Growth Inhibition Assay - 86K Screen [AID598, Type: screening] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Human H69AR Lung Tumor Cell Growth Inhibition Assay - 86K Screen | | AID | 598 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 24 | [SID7970631] | Active | EC50 | | Fluorescent HTS Cytotoxicity/Cell viability assay (HPDE-C7 cells) [AID430, Type: confirmatory] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | EC50 | [uM] | | BioAssay | Fluorescent HTS Cytotoxicity/Cell viability assay (HPDE-C7 cells) | | AID | 430 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 25 | [SID7970631] | Active | | | Cell Proliferation & Viability (Cytotoxicity) Primary Assay 60K MLSMR [AID463, Type: screening] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Cell Proliferation & Viability (Cytotoxicity) Primary Assay 60K MLSMR | | AID | 463 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 26 | [SID7970631] | Active | | | Cell Proliferation & Viability (Cytotoxicity) Dose Response Assay 60K MLSMR [AID464, Type: confirmatory] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Cell Proliferation & Viability (Cytotoxicity) Dose Response Assay 60K MLSMR | | AID | 464 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 27 | [SID7970631] | Active | | | Counterscreen for inhibitors of Janus kinase 2 mutant JAK2V617F: Cell-based high throughput assay to identify inhibitors of parental Ba/F3 cell viability. [AID1486, Type: screening] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of Janus kinase 2 mutant JAK2V617F: Cell-based high throughput assay to identify inhibitors of parental Ba/F3 cell viability. | | AID | 1486 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 28 | [SID7970631] | Active | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors [AID1813, Type: screening] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors | | AID | 1813 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 29 | [SID7970631] | Active | | | Single concentration confirmation of inhibitors of Mdm2/MdmX interaction using a Brca1/Bard1 BiLC Counterscreen assay. [AID504668, Type: screening] | Breast cancer type 1 susceptibility protein [gi:728984] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Mdm2/MdmX interaction using a Brca1/Bard1 BiLC Counterscreen assay. | | AID | 504668 | | BioAssay type | screening | | Target | Breast cancer type 1 susceptibility protein [gi:728984] | | PubMed | | | Data Table |  |
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| 30 | [SID7970631] | Active | | | Single concentration confirmation of inhibitors of Mdm2/MdmX interaction using a Brca1/Bard1 BiLC Counterscreen assay. [AID504668, Type: screening] | Breast cancer type 1 susceptibility protein [gi:728984] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Mdm2/MdmX interaction using a Brca1/Bard1 BiLC Counterscreen assay. | | AID | 504668 | | BioAssay type | screening | | Target | Breast cancer type 1 susceptibility protein [gi:728984] | | PubMed | | | Data Table |  |
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| 31 | [SID56436611] | Active | | | Single concentration confirmation of small molecule Triacylglycerol inhbitors in a fluoresence assay [AID651629, Type: screening] | |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 56436611 | | CID | 4289057 | | Outcome | Active | | BioAssay | Single concentration confirmation of small molecule Triacylglycerol inhbitors in a fluoresence assay | | AID | 651629 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 32 | [SID56436611] | Active | | | uHTS identification of small molecule Triacylglycerol inhbitors in a fluoresence assay [AID651582, Type: screening] | |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 56436611 | | CID | 4289057 | | Outcome | Active | | BioAssay | uHTS identification of small molecule Triacylglycerol inhbitors in a fluoresence assay | | AID | 651582 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 33 | [SID7970631] | Active | | | Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID600, Type: confirmatory] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 600 | | BioAssay type | confirmatory | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 34 | [SID7970631] | Active | | | Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID600, Type: confirmatory] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 600 | | BioAssay type | confirmatory | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 35 | [SID7970631] | Active | | | Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID600, Type: confirmatory] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 600 | | BioAssay type | confirmatory | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 36 | [SID7970631] | Active | | | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID525, Type: screening] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 525 | | BioAssay type | screening | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 37 | [SID7970631] | Active | | | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID525, Type: screening] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 525 | | BioAssay type | screening | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 38 | [SID7970631] | Active | | | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID525, Type: screening] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 525 | | BioAssay type | screening | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 39 | [SID56436611] | Active | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504692, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 56436611 | | CID | 4289057 | | Outcome | Active | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504692 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
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| 40 | [SID56436611] | Active | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504692, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 56436611 | | CID | 4289057 | | Outcome | Active | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504692 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
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| 41 | [SID56436611] | Active | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504692, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 56436611 | | CID | 4289057 | | Outcome | Active | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504692 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
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| 42 | [SID7970631] | Active | | | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F [AID1446, Type: screening] | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | | AID | 1446 | | BioAssay type | screening | | Target | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] | | PubMed | | | Data Table |  |
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| 43 | [SID7970631] | Active | | | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F [AID1446, Type: screening] | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | | AID | 1446 | | BioAssay type | screening | | Target | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] | | PubMed | | | Data Table |  |
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| 44 | [SID7970631] | Active | | | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F [AID1446, Type: screening] | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | | AID | 1446 | | BioAssay type | screening | | Target | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] | | PubMed | | | Data Table |  |
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| 45 | [SID7970631] | Active | IC50 | | High Throughput Imaging Assay for Beta-Catenin [AID1665, Type: confirmatory] | catenin beta-1 [Homo sapiens] [gi:4503131] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | IC50 | [uM] | | BioAssay | High Throughput Imaging Assay for Beta-Catenin | | AID | 1665 | | BioAssay type | confirmatory | | Target | catenin beta-1 [Homo sapiens] [gi:4503131] | | PubMed | | | Data Table |  |
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| 46 | [SID7970631] | Active | IC50 | | High Throughput Imaging Assay for Beta-Catenin [AID1665, Type: confirmatory] | catenin beta-1 [Homo sapiens] [gi:4503131] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | IC50 | [uM] | | BioAssay | High Throughput Imaging Assay for Beta-Catenin | | AID | 1665 | | BioAssay type | confirmatory | | Target | catenin beta-1 [Homo sapiens] [gi:4503131] | | PubMed | | | Data Table |  |
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| 47 | [SID7970631] | Active | | | HCS assay for microtubule stabilizers [AID2205, Type: screening] | tubulin, beta [Homo sapiens] [gi:29788785] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | HCS assay for microtubule stabilizers | | AID | 2205 | | BioAssay type | screening | | Target | tubulin, beta [Homo sapiens] [gi:29788785] | | PubMed | | | Data Table |  |
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| 48 | [SID7970631] | Active | | | HCS assay for microtubule stabilizers [AID2205, Type: screening] | tubulin, beta [Homo sapiens] [gi:29788785] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | HCS assay for microtubule stabilizers | | AID | 2205 | | BioAssay type | screening | | Target | tubulin, beta [Homo sapiens] [gi:29788785] | | PubMed | | | Data Table |  |
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| 49 | [SID7970631] | Active | | | Single concentration confirmation of uHTS for Inhibitors of Mdm2/MdmX interaction in luminescent format. [AID489028, Type: screening] | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS for Inhibitors of Mdm2/MdmX interaction in luminescent format. | | AID | 489028 | | BioAssay type | screening | | Target | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] | | PubMed | | | Data Table |  |
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| 50 | [SID7970631] | Active | | | Single concentration confirmation of uHTS for Inhibitors of Mdm2/MdmX interaction in luminescent format. [AID489028, Type: screening] | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 7970631 | | CID | 4289057 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS for Inhibitors of Mdm2/MdmX interaction in luminescent format. | | AID | 489028 | | BioAssay type | screening | | Target | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] | | PubMed | | | Data Table |  |
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