| 1 | [SID14742351] | Active | Potency | 6.147 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: V1B Hit Validation [AID492948, Type: confirmatory] | vasopressin V1b receptor [Homo sapiens] [gi:4502333] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 6.147 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: V1B Hit Validation | | AID | 492948 | | BioAssay type | confirmatory | | Target | vasopressin V1b receptor [Homo sapiens] [gi:4502333] | | PubMed | | | Data Table |  |
|
| 2 | [SID14742351] | Active | Potency | 6.147 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: V1B Hit Validation [AID492948, Type: confirmatory] | vasopressin V1b receptor [Homo sapiens] [gi:4502333] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 6.147 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: V1B Hit Validation | | AID | 492948 | | BioAssay type | confirmatory | | Target | vasopressin V1b receptor [Homo sapiens] [gi:4502333] | | PubMed | | | Data Table |  |
|
| 3 | [SID14742351] | Active | Potency | 6.147 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: V1B Hit Validation [AID492948, Type: confirmatory] | vasopressin V1b receptor [Homo sapiens] [gi:4502333] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 6.147 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: V1B Hit Validation | | AID | 492948 | | BioAssay type | confirmatory | | Target | vasopressin V1b receptor [Homo sapiens] [gi:4502333] | | PubMed | | | Data Table |  |
|
| 4 | [SID14742351] | Active | Potency | 12.5893 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 5 | [SID14742351] | Active | Potency | 12.5893 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 6 | [SID14742351] | Active | Potency | 14.1254 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 [AID2676, Type: confirmatory] | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 | | AID | 2676 | | BioAssay type | confirmatory | | Target | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] | | PubMed | | | Data Table |  |
|
| 7 | [SID14742351] | Active | Potency | 14.1254 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 [AID2676, Type: confirmatory] | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 | | AID | 2676 | | BioAssay type | confirmatory | | Target | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] | | PubMed | | | Data Table |  |
|
| 8 | [SID14742351] | Active | Potency | 16.9441 | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) [AID588342, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 16.9441 [uM] | | BioAssay | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) | | AID | 588342 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
|
| 9 | [SID14742351] | Active | Potency | 17.7828 | qHTS of TDP-43 Inhibitors [AID652104, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | qHTS of TDP-43 Inhibitors | | AID | 652104 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 10 | [SID14742351] | Active | Potency | 19.4384 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: RXFP2 Hit Validation [AID489043, Type: confirmatory] | relaxin receptor 2 isoform 1 [Homo sapiens] [gi:18677729] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 19.4384 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: RXFP2 Hit Validation | | AID | 489043 | | BioAssay type | confirmatory | | Target | relaxin receptor 2 isoform 1 [Homo sapiens] [gi:18677729] | | PubMed | | | Data Table |  |
|
| 11 | [SID14742351] | Active | Potency | 19.4384 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: RXFP2 Hit Validation [AID489043, Type: confirmatory] | relaxin receptor 2 isoform 1 [Homo sapiens] [gi:18677729] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 19.4384 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: RXFP2 Hit Validation | | AID | 489043 | | BioAssay type | confirmatory | | Target | relaxin receptor 2 isoform 1 [Homo sapiens] [gi:18677729] | | PubMed | | | Data Table |  |
|
| 12 | [SID14742351] | Active | Potency | 19.4384 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: THP1 Hit Validation [AID492949, Type: confirmatory] | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 19.4384 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: THP1 Hit Validation | | AID | 492949 | | BioAssay type | confirmatory | | Target | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] | | PubMed | | | Data Table |  |
|
| 13 | [SID14742351] | Active | Potency | 19.4384 | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: THP1 Hit Validation [AID492949, Type: confirmatory] | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | Potency | 19.4384 [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1: THP1 Hit Validation | | AID | 492949 | | BioAssay type | confirmatory | | Target | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] | | PubMed | | | Data Table |  |
|
| 14 | [SID14742351] | Active | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 15 | [SID14742351] | Active | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 16 | [SID14742351] | Active | | | Screening for Modulators of Post-Golgi Transport, Control Strain [AID738, Type: screening] | |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | BioAssay | Screening for Modulators of Post-Golgi Transport, Control Strain | | AID | 738 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 17 | [SID14742351] | Active | | | Modulators of the EP2 prostaglandin E2 receptor - Primary Screening [AID940, Type: screening] | prostaglandin E receptor 2 (subtype EP2), 53kDa [Homo sapiens] [gi:31881630] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | BioAssay | Modulators of the EP2 prostaglandin E2 receptor - Primary Screening | | AID | 940 | | BioAssay type | screening | | Target | prostaglandin E receptor 2 (subtype EP2), 53kDa [Homo sapiens] [gi:31881630] | | PubMed | | | Data Table |  |
|
| 18 | [SID14742351] | Active | | | Modulators of the EP2 prostaglandin E2 receptor - Primary Screening [AID940, Type: screening] | prostaglandin E receptor 2 (subtype EP2), 53kDa [Homo sapiens] [gi:31881630] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Active | | BioAssay | Modulators of the EP2 prostaglandin E2 receptor - Primary Screening | | AID | 940 | | BioAssay type | screening | | Target | prostaglandin E receptor 2 (subtype EP2), 53kDa [Homo sapiens] [gi:31881630] | | PubMed | | | Data Table |  |
|
| 19 | [SID14742351] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 20 | [SID14742351] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 21 | [SID14742351] | Unspecified | Potency | | Activators of T cell receptors: qHTS campaign [AID504894, Type: confirmatory] | T cell receptor [Homo sapiens] [gi:553160] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | Activators of T cell receptors: qHTS campaign | | AID | 504894 | | BioAssay type | confirmatory | | Target | T cell receptor [Homo sapiens] [gi:553160] | | PubMed | | | Data Table |  |
|
| 22 | [SID14742351] | Unspecified | | | 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. | 22 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Unspecified | | 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 |  |
|
| 23 | [SID14742351] | Unspecified | | | 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. | 23 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Unspecified | | 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 |  |
|
| 24 | [SID14742351] | Unspecified | | | 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. | 24 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Unspecified | | 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 |  |
|
| 25 | [SID14742351] | Inactive | Potency | 8.9125 | qHTS Assay for Inhibitors of Influenza NS1 Protein Function [AID2326, Type: confirmatory] | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | 8.9125 [uM] | | BioAssay | qHTS Assay for Inhibitors of Influenza NS1 Protein Function | | AID | 2326 | | BioAssay type | confirmatory | | Target | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] | | PubMed | | | Data Table |  |
|
| 26 | [SID14742351] | Inactive | Potency | 28.1838 | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | | AID | 624417 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
|
| 27 | [SID14742351] | Inactive | Potency | 28.1838 | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | | AID | 624417 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
|
| 28 | [SID14742351] | Inactive | Potency | | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Glutaminase (GLS) | | AID | 624170 | | BioAssay type | confirmatory | | Target | GLS protein [Homo sapiens] [gi:71051501] | | PubMed | | | Data Table |  |
|
| 29 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. [AID1440, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. | | AID | 1440 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 30 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. [AID1440, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. | | AID | 1440 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 31 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. [AID1440, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. | | AID | 1440 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 32 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1441, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1441 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 33 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1441, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1441 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 34 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1441, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1441 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 35 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 36 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 37 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 38 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1415, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1415 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
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| 39 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1415, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1415 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
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| 40 | [SID14742351] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1415, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1415 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
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| 41 | [SID14742351] | Inactive | Potency | | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) [AID652105, Type: confirmatory] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) | | AID | 652105 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 42 | [SID14742351] | Inactive | Potency | | qHTS of alpha-syn Inhibitors [AID652106, Type: confirmatory] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of alpha-syn Inhibitors | | AID | 652106 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 43 | [SID14742351] | Inactive | Potency | | 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. | 43 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | [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 |  |
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| 44 | [SID14742351] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | [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 | | | PubMed | | | Data Table |  |
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| 45 | [SID14742351] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | Potency | [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 | | | PubMed | | | Data Table |  |
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| 46 | [SID14742351] | Inactive | | | uHTS identification of small molecule Triacylglycerol inhbitors in a fluoresence assay [AID651582, Type: screening] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | 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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| 47 | [SID14742351] | Inactive | | | Counter Screen for Glucose-6-Phosphate Dehydrogenase-based Primary Assay [AID1020, Type: screening] | glucose-6-phosphate dehydrogenase [Leuconostoc mesenteroides] [gi:149631] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Counter Screen for Glucose-6-Phosphate Dehydrogenase-based Primary Assay | | AID | 1020 | | BioAssay type | screening | | Target | glucose-6-phosphate dehydrogenase [Leuconostoc mesenteroides] [gi:149631] | | PubMed | | | Data Table |  |
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| 48 | [SID14742351] | Inactive | | | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) [AID488975, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) | | AID | 488975 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
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| 49 | [SID14742351] | Inactive | | | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) [AID488975, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) | | AID | 488975 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
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| 50 | [SID14742351] | Inactive | | | Primary cell-based screen for identification of compounds that allosterically activate the Choline Transporter (CHT) [AID488977, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 14742351 | | CID | 23663726 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that allosterically activate the Choline Transporter (CHT) | | AID | 488977 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
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