| 1 | [SID17389499] | Active | | | Caspase-3/7 Activation Profiling of Human Lymphoblast Cell Lines [AID588813_49, Type: other] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Active | | BioAssay | Caspase-3/7 Activation Profiling of Human Lymphoblast Cell Lines | | AID | 588813 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 2 | [SID56436642] | Active | | | uHTS Fluorescent Assay Using Nedd8 Protein Substrate for Identification of Inhibitors of Sentrin-Specific Protease 8 (SENP8) [AID602440, Type: screening] | SENP8 gene product [Homo sapiens] [gi:262118306] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Active | | BioAssay | uHTS Fluorescent Assay Using Nedd8 Protein Substrate for Identification of Inhibitors of Sentrin-Specific Protease 8 (SENP8) | | AID | 602440 | | BioAssay type | screening | | Target | SENP8 gene product [Homo sapiens] [gi:262118306] | | PubMed | | | Data Table |  |
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| 3 | [SID56436642] | 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. | 3 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | 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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| 4 | [SID56436642] | 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. | 4 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | 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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| 5 | [SID17389499] | Unspecified | | | Cell Viability Profiling of Human Lymphoblast Cell Lines [AID588812, Type: other] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Unspecified | | BioAssay | Cell Viability Profiling of Human Lymphoblast Cell Lines | | AID | 588812 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 6 | [SID17389499] | Unspecified | | | Caspase-3/7 Activation Profiling of Human Lymphoblast Cell Lines [AID588813, Type: other] | |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Unspecified | | BioAssay | Caspase-3/7 Activation Profiling of Human Lymphoblast Cell Lines | | AID | 588813 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 7 | [SID17389499] | Unspecified | | | qHTS assay for identifying genotoxic compounds that show differential cytotoxicity against a panel of isogenic chicken DT40 cell lines with known DNA damage response pathways [AID651838, Type: other] | |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Unspecified | | BioAssay | qHTS assay for identifying genotoxic compounds that show differential cytotoxicity against a panel of isogenic chicken DT40 cell lines with known DNA damage response pathways | | AID | 651838 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 8 | [SID14719324] | Inactive | Potency | 10.4179 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | Potency | 10.4179 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | | AID | 504832 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 9 | [SID14719324] | Inactive | Potency | 13.1154 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | Potency | 13.1154 [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 |  |
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| 10 | [SID56436642] | Inactive | Potency | 56.2341 | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain [AID504339, Type: confirmatory] | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | 56.2341 [uM] | | BioAssay | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain | | AID | 504339 | | BioAssay type | confirmatory | | Target | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] | | PubMed | | | Data Table |  |
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| 11 | [SID56436642] | Inactive | Potency | 79.4328 | HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails [AID540317, Type: confirmatory] | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | 79.4328 [uM] | | BioAssay | HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails | | AID | 540317 | | BioAssay type | confirmatory | | Target | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] | | PubMed | | | Data Table |  |
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| 12 | [SID14719324] | Inactive | Potency | 89.1251 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | Potency | 89.1251 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
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| 13 | [SID56436642] | Inactive | | | Hedgehog Measured in Biochemical System Using Plate Reader - 2070-01_Inhibitor_SinglePoint_HTS_Activity [AID588832, Type: screening] | hedgehog, isoform A [Drosophila melanogaster] [gi:7300964] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Hedgehog Measured in Biochemical System Using Plate Reader - 2070-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 588832 | | BioAssay type | screening | | Target | hedgehog, isoform A [Drosophila melanogaster] [gi:7300964] | | PubMed | | | Data Table |  |
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| 14 | [SID56436642] | Inactive | | | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1) [AID624377, Type: screening] | ASAP1 gene product [Homo sapiens] [gi:351542238] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1) | | AID | 624377 | | BioAssay type | screening | | Target | ASAP1 gene product [Homo sapiens] [gi:351542238] | | PubMed | | | Data Table |  |
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| 15 | [SID56436642] | Inactive | Potency | | 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. | 15 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [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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| 16 | [SID56436642] | Inactive | Potency | | 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. | 16 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [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 |  |
|
| 17 | [SID56436642] | Inactive | | | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) [AID602281, Type: screening] | ABHD5 gene product [Homo sapiens] [gi:31542303] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) | | AID | 602281 | | BioAssay type | screening | | Target | ABHD5 gene product [Homo sapiens] [gi:31542303] | | PubMed | | | Data Table |  |
|
| 18 | [SID14719324] | Inactive | | | Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 [AID488922, Type: screening] | KCNK9 gene product [Homo sapiens] [gi:7706135] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | | AID | 488922 | | BioAssay type | screening | | Target | KCNK9 gene product [Homo sapiens] [gi:7706135] | | PubMed | | | Data Table |  |
|
| 19 | [SID124812472] | Inactive | | | A screen for small molecule inhibitors of the human deubiquitinating enzyme, UCH37 [AID588478, Type: other] | ubiquitin C-terminal hydrolase UCH37 [Homo sapiens] [gi:4877999] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 124812472 | | CID | 6782 | | Outcome | Inactive | | BioAssay | A screen for small molecule inhibitors of the human deubiquitinating enzyme, UCH37 | | AID | 588478 | | BioAssay type | other | | Target | ubiquitin C-terminal hydrolase UCH37 [Homo sapiens] [gi:4877999] | | PubMed | | | Data Table |  |
|
| 20 | [SID56436642] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Phosphatase Methylesterase 1 (PME-1). [AID2130, Type: screening] | protein phosphatase methylesterase 1 [Homo sapiens] [gi:7706645] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Phosphatase Methylesterase 1 (PME-1). | | AID | 2130 | | BioAssay type | screening | | Target | protein phosphatase methylesterase 1 [Homo sapiens] [gi:7706645] | | PubMed | | | Data Table |  |
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| 21 | [SID56436642] | Inactive | Potency | | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 22 | [SID56436642] | Inactive | Potency | | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 23 | [SID56436642] | Inactive | | | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity [AID652197, Type: screening] | ERAP1 protein [Homo sapiens] [gi:21315078] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 652197 | | BioAssay type | screening | | Target | ERAP1 protein [Homo sapiens] [gi:21315078] | | PubMed | | | Data Table |  |
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| 24 | [SID56436642] | Inactive | | | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity [AID652197, Type: screening] | ERAP1 protein [Homo sapiens] [gi:21315078] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 652197 | | BioAssay type | screening | | Target | ERAP1 protein [Homo sapiens] [gi:21315078] | | PubMed | | | Data Table |  |
|
| 25 | [SID56436642] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. [AID504734, Type: screening] | toll-like receptor 9 [Homo sapiens] [gi:194068499] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | | AID | 504734 | | BioAssay type | screening | | Target | toll-like receptor 9 [Homo sapiens] [gi:194068499] | | PubMed | | | Data Table |  |
|
| 26 | [SID56436642] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. [AID504734, Type: screening] | toll-like receptor 9 [Homo sapiens] [gi:194068499] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of TLR9-MyD88 binding. | | AID | 504734 | | BioAssay type | screening | | Target | toll-like receptor 9 [Homo sapiens] [gi:194068499] | | PubMed | | | Data Table |  |
|
| 27 | [SID14719324] | Inactive | | | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504810, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504810 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
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| 28 | [SID14719324] | Inactive | | | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504810, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504810 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|
| 29 | [SID14719324] | Inactive | | | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504810, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504810 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|
| 30 | [SID14719324] | Inactive | | | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504812, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504812 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|
| 31 | [SID14719324] | Inactive | | | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504812, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504812 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|
| 32 | [SID14719324] | Inactive | | | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504812, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504812 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|
| 33 | [SID14719324] | Inactive | IC50 | | uHTS HTRF assay for identification of inhibitors of SUMOylation [AID2006, Type: confirmatory] | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | uHTS HTRF assay for identification of inhibitors of SUMOylation | | AID | 2006 | | BioAssay type | confirmatory | | Target | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] | | PubMed | | | Data Table |  |
|
| 34 | [SID14719324] | Inactive | | | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay [AID485273, Type: screening] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | | AID | 485273 | | BioAssay type | screening | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
|
| 35 | [SID14719324] | Inactive | | | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay [AID485273, Type: screening] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 14719324 | | CID | 6782 | | Outcome | Inactive | | BioAssay | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | | AID | 485273 | | BioAssay type | screening | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
|
| 36 | [SID56436642] | Inactive | | | uHTS identification of SUMO1-mediated protein-protein interactions [AID602429, Type: screening] | SUMO-1 [Homo sapiens] [gi:1762973] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | uHTS identification of SUMO1-mediated protein-protein interactions | | AID | 602429 | | BioAssay type | screening | | Target | SUMO-1 [Homo sapiens] [gi:1762973] | | PubMed | | | Data Table |  |
|
| 37 | [SID56436642] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 38 | [SID56436642] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 39 | [SID56436642] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 40 | [SID56436642] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 41 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 42 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 43 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 44 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 45 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 46 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 47 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 48 | [SID17389499] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 17389499 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
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| 49 | [SID56436642] | Inactive | | | uHTS identification of small molecule inhibitors of Csn-mediated Deneddylation of Cullin-Ring Ligases, vis a fluorescence polarization assay [AID651999, Type: screening] | COPS5 gene product [Homo sapiens] [gi:38027923] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of Csn-mediated Deneddylation of Cullin-Ring Ligases, vis a fluorescence polarization assay | | AID | 651999 | | BioAssay type | screening | | Target | COPS5 gene product [Homo sapiens] [gi:38027923] | | PubMed | | | Data Table |  |
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| 50 | [SID56436642] | Inactive | Potency | | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 56436642 | | CID | 6782 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
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