| 1 | [SID57268340] | Active | Potency | 89.1251 | 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. | 1 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Active | | Potency | 89.1251 [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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| 2 | [SID103681719] | Active | | | Inhibition of human mitochondrial NADP-ME E59L mutant expressed in Escherichia coli XL-1 assessed as residual enzyme activity by spectrophotometry in presence of fumarate [AID429164, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103681719 | | CID | 444266 | | Outcome | Active | | BioAssay | Inhibition of human mitochondrial NADP-ME E59L mutant expressed in Escherichia coli XL-1 assessed as residual enzyme activity by spectrophotometry in presence of fumarate | | AID | 429164 | | BioAssay type | Literature | | Target | | | PubMed | 19595601 | | Data Table |  |
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| 3 | [SID103681719] | Active | | | Inhibition of human mitochondrial NADP-ME E59L mutant expressed in Escherichia coli XL-1 assessed as residual enzyme activity by spectrophotometry in absence of fumarate [AID429165, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103681719 | | CID | 444266 | | Outcome | Active | | BioAssay | Inhibition of human mitochondrial NADP-ME E59L mutant expressed in Escherichia coli XL-1 assessed as residual enzyme activity by spectrophotometry in absence of fumarate | | AID | 429165 | | BioAssay type | Literature | | Target | | | PubMed | 19595601 | | Data Table |  |
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| 4 | [SID46393252] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Maleic Acid-bound Structure Of Srhept Mutant Of E. Coli Aspartate Aminotransferase [gi:55669978] |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 46393252 | | CID | 444266 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Maleic Acid-bound Structure Of Srhept Mutant Of E. Coli Aspartate Aminotransferase [gi:55669978] | | PubMed | 15461450 | | Data Table |  |
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| 5 | [SID103681719] | Active | | | Inhibition of wild type human recombinant mitochondrial NADP-ME expressed in Escherichia coli BL21 assessed as residual enzyme activity by spectrophotometry in absence of fumarate [AID429166, Type: Literature] | NADP-dependent malic enzyme, mitochondrial [gi:215274021] |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103681719 | | CID | 444266 | | Outcome | Active | | BioAssay | Inhibition of wild type human recombinant mitochondrial NADP-ME expressed in Escherichia coli BL21 assessed as residual enzyme activity by spectrophotometry in absence of fumarate | | AID | 429166 | | BioAssay type | Literature | | Target | NADP-dependent malic enzyme, mitochondrial [gi:215274021] | | PubMed | 19595601 | | Data Table |  |
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| 6 | [SID46391428] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Aspartate Aminotransferase Hexamutant [gi:1127182] |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 46391428 | | CID | 444266 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Aspartate Aminotransferase Hexamutant [gi:1127182] | | PubMed | 7664122 | | Data Table |  |
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| 7 | [SID103681719] | Unspecified | | | Literature-mined public compounds from Greene et al multi-species hepatotoxicity modelling dataset [AID588209, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103681719 | | CID | 444266 | | Outcome | Unspecified | | BioAssay | Literature-mined public compounds from Greene et al multi-species hepatotoxicity modelling dataset | | AID | 588209 | | BioAssay type | Literature | | Target | | | PubMed | 20553011 | | Data Table |  |
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| 8 | [SID103681719] | Unspecified | | | Human drug-induced liver injury (DILI) modelling dataset from Ekins et al [AID588210, Type: Literature] | |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103681719 | | CID | 444266 | | Outcome | Unspecified | | BioAssay | Human drug-induced liver injury (DILI) modelling dataset from Ekins et al | | AID | 588210 | | BioAssay type | Literature | | Target | | | PubMed | 20843939 | | Data Table |  |
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| 9 | [SID17389671] | 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. | 9 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | 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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| 10 | [SID57268340] | 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. | 10 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | 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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| 11 | [SID57268340] | 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. | 11 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | 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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| 12 | [SID57268340] | Inactive | Potency | 1.122 | 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 | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | 1.122 [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 | [SID57268340] | Inactive | Potency | 1.636 | 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. | 13 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | 1.636 [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 |  |
|
| 14 | [SID57268340] | Inactive | Potency | 5.6234 | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction [AID624246, Type: confirmatory] | ERG gene product [Homo sapiens] [gi:343478176] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | 5.6234 [uM] | | BioAssay | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction | | AID | 624246 | | BioAssay type | confirmatory | | Target | ERG gene product [Homo sapiens] [gi:343478176] | | PubMed | | | Data Table |  |
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| 15 | [SID57268340] | Inactive | Potency | 5.6234 | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction [AID624246, Type: confirmatory] | ERG gene product [Homo sapiens] [gi:343478176] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | 5.6234 [uM] | | BioAssay | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction | | AID | 624246 | | BioAssay type | confirmatory | | Target | ERG gene product [Homo sapiens] [gi:343478176] | | PubMed | | | Data Table |  |
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| 16 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
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| 17 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 18 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 19 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 20 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling [AID588513, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling | | AID | 588513 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 21 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling [AID588513, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling | | AID | 588513 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 22 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling [AID588513, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling | | AID | 588513 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 23 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling [AID588513, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of estrogen receptor alpha signaling | | AID | 588513 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 24 | [SID57268340] | Inactive | Potency | | qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2 [AID488837, Type: confirmatory] | eyes absent homolog 2 isoform a [Homo sapiens] [gi:26667227] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2 | | AID | 488837 | | BioAssay type | confirmatory | | Target | eyes absent homolog 2 isoform a [Homo sapiens] [gi:26667227] | | PubMed | | | Data Table |  |
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| 25 | [SID57268340] | Inactive | | | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay [AID602261, Type: screening] | FASN gene product [Homo sapiens] [gi:41872631] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay | | AID | 602261 | | BioAssay type | screening | | Target | FASN gene product [Homo sapiens] [gi:41872631] | | PubMed | | | Data Table |  |
|
| 26 | [SID57268340] | Inactive | | | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay [AID602261, Type: screening] | FASN gene product [Homo sapiens] [gi:41872631] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay | | AID | 602261 | | BioAssay type | screening | | Target | FASN gene product [Homo sapiens] [gi:41872631] | | PubMed | | | Data Table |  |
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| 27 | [SID57268340] | Inactive | | | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay [AID602261, Type: screening] | FASN gene product [Homo sapiens] [gi:41872631] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay | | AID | 602261 | | BioAssay type | screening | | Target | FASN gene product [Homo sapiens] [gi:41872631] | | PubMed | | | Data Table |  |
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| 28 | [SID57268340] | Inactive | Potency | | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). [AID588795, Type: confirmatory] | flap endonuclease 1 [Homo sapiens] [gi:4758356] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). | | AID | 588795 | | BioAssay type | confirmatory | | Target | flap endonuclease 1 [Homo sapiens] [gi:4758356] | | PubMed | | | Data Table |  |
|
| 29 | [SID57268340] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) [AID602396, Type: screening] | NR5A2 gene product [Homo sapiens] [gi:4504343] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) | | AID | 602396 | | BioAssay type | screening | | Target | NR5A2 gene product [Homo sapiens] [gi:4504343] | | PubMed | | | Data Table |  |
|
| 30 | [SID57268340] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) [AID602396, Type: screening] | NR5A2 gene product [Homo sapiens] [gi:4504343] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) | | AID | 602396 | | BioAssay type | screening | | Target | NR5A2 gene product [Homo sapiens] [gi:4504343] | | PubMed | | | Data Table |  |
|
| 31 | [SID17389671] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
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| 32 | [SID17389671] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
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| 33 | [SID17389671] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 34 | [SID57268340] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 35 | [SID57268340] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 36 | [SID17389671] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 37 | [SID17389671] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 38 | [SID57268340] | Inactive | Potency | | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 39 | [SID57268340] | Inactive | Potency | | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 40 | [SID57268340] | Inactive | | | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS [AID485317, Type: screening] | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | BioAssay | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS | | AID | 485317 | | BioAssay type | screening | | Target | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] | | PubMed | | | Data Table |  |
|
| 41 | [SID17389671] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 42 | [SID17389671] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 43 | [SID57268340] | Inactive | Potency | | qHTS of GLP-1 Receptor Agonists [AID624172, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of GLP-1 Receptor Agonists | | AID | 624172 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
|
| 44 | [SID57268340] | Inactive | Potency | | qHTS of GLP-1 Receptor Agonists [AID624172, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of GLP-1 Receptor Agonists | | AID | 624172 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
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| 45 | [SID57268340] | Inactive | Potency | | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [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 |  |
|
| 46 | [SID57268340] | Inactive | Potency | | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [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 |  |
|
| 47 | [SID57268340] | Inactive | Potency | | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | 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 |  |
|
| 48 | [SID57268340] | Inactive | Potency | | qHTS for Antagonists of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS [AID624288, Type: confirmatory] | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 57268340 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Antagonists of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS | | AID | 624288 | | BioAssay type | confirmatory | | Target | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] | | PubMed | | | Data Table |  |
|
| 49 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule agonists of glucocorticoid receptor signaling [AID588532, Type: confirmatory] | glucocorticoid receptor [Homo sapiens] [gi:311348376] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of glucocorticoid receptor signaling | | AID | 588532 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor [Homo sapiens] [gi:311348376] | | PubMed | | | Data Table |  |
|
| 50 | [SID17389671] | Inactive | Potency | | qHTS assay for small molecule agonists of glucocorticoid receptor signaling [AID588532, Type: confirmatory] | glucocorticoid receptor [Homo sapiens] [gi:311348376] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 17389671 | | CID | 444266 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of glucocorticoid receptor signaling | | AID | 588532 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor [Homo sapiens] [gi:311348376] | | PubMed | | | Data Table |  |
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