| 1 | [SID847772] | Active | IC50 | 4.67 | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target [AID521, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 4.67 [uM] | | BioAssay | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target | | AID | 521 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 2 | [SID847772] | Active | IC50 | 4.67 | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target [AID521, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 4.67 [uM] | | BioAssay | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target | | AID | 521 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 3 | [SID847772] | Active | IC50 | 4.67 | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target [AID521, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 4.67 [uM] | | BioAssay | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target | | AID | 521 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 4 | [SID847772] | Active | Potency | 5.2213 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | Potency | 5.2213 [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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| 5 | [SID26669159] | Active | Potency | 6.3096 | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 26669159 | | CID | 6602529 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS for Inhibitors of Glutaminase (GLS) | | AID | 624170 | | BioAssay type | confirmatory | | Target | GLS protein [Homo sapiens] [gi:71051501] | | PubMed | | | Data Table |  |
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| 6 | [SID847772] | Active | IC50 | 9.462 | SMAD Transcription Factor Inhibitors Dose Response Confirmation [AID715, Type: confirmatory] | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 9.462 [uM] | | BioAssay | SMAD Transcription Factor Inhibitors Dose Response Confirmation | | AID | 715 | | BioAssay type | confirmatory | | Target | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] | | PubMed | | | Data Table |  |
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| 7 | [SID847772] | Active | IC50 | 9.462 | SMAD Transcription Factor Inhibitors Dose Response Confirmation [AID715, Type: confirmatory] | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 9.462 [uM] | | BioAssay | SMAD Transcription Factor Inhibitors Dose Response Confirmation | | AID | 715 | | BioAssay type | confirmatory | | Target | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] | | PubMed | | | Data Table |  |
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| 8 | [SID847772] | Active | IC50 | 11.4 | TR-FRET secondary assay for HTS discovery of chemical inhibitors of Hsp70 [AID786, Type: confirmatory] | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 11.4 [uM] | | BioAssay | TR-FRET secondary assay for HTS discovery of chemical inhibitors of Hsp70 | | AID | 786 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] | | PubMed | | | Data Table |  |
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| 9 | [SID847772] | Active | IC50 | 15.6568 | Tumor Hsp90 Inhibitors Dose Response Confirmation [AID712, Type: confirmatory] | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 15.6568 [uM] | | BioAssay | Tumor Hsp90 Inhibitors Dose Response Confirmation | | AID | 712 | | BioAssay type | confirmatory | | Target | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] | | PubMed | | | Data Table |  |
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| 10 | [SID847772] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
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| 11 | [SID847772] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
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| 12 | [SID847772] | Active | IC50 | 45.4 | High Throughput Screening Assay for Hsp70 Inhibitors [AID583, Type: confirmatory] | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | 45.4 [uM] | | BioAssay | High Throughput Screening Assay for Hsp70 Inhibitors | | AID | 583 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] | | PubMed | | | Data Table |  |
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| 13 | [SID847772] | Active | | | 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. | 13 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | 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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| 14 | [SID847772] | Active | | | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) [AID727, Type: screening] | Focal adhesion kinase 1 [gi:3183518] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) | | AID | 727 | | BioAssay type | screening | | Target | Focal adhesion kinase 1 [gi:3183518] | | PubMed | | | Data Table |  |
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| 15 | [SID847772] | Active | | | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) [AID727, Type: screening] | Focal adhesion kinase 1 [gi:3183518] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) | | AID | 727 | | BioAssay type | screening | | Target | Focal adhesion kinase 1 [gi:3183518] | | PubMed | | | Data Table |  |
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| 16 | [SID847772] | Active | | | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide [AID686964, Type: screening] | Methyl-CpG binding domain protein 2 [Homo sapiens] [gi:21595776] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide | | AID | 686964 | | BioAssay type | screening | | Target | Methyl-CpG binding domain protein 2 [Homo sapiens] [gi:21595776] | | PubMed | | | Data Table |  |
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| 17 | [SID847772] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 18 | [SID847772] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 19 | [SID847772] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 20 | [SID847772] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 21 | [SID847772] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 22 | [SID847772] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 23 | [SID847772] | Active | IC50 | | Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay [AID2073, Type: confirmatory] | Mint1 [Rattus norvegicus] [gi:2625023] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | IC50 | [uM] | | BioAssay | Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | | AID | 2073 | | BioAssay type | confirmatory | | Target | Mint1 [Rattus norvegicus] [gi:2625023] | | PubMed | | | Data Table |  |
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| 24 | [SID847772] | Active | | | uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) [AID1274, Type: screening] | neutrophil cytosolic factor 1 [Homo sapiens] [gi:115298672] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) | | AID | 1274 | | BioAssay type | screening | | Target | neutrophil cytosolic factor 1 [Homo sapiens] [gi:115298672] | | PubMed | | | Data Table |  |
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| 25 | [SID847772] | Active | | | uHTS for 14-3-3/Bad interaction inhibitors [AID781, Type: screening] | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide [Bos taurus [gi:27807367] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS for 14-3-3/Bad interaction inhibitors | | AID | 781 | | BioAssay type | screening | | Target | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide [Bos taurus [gi:27807367] | | PubMed | | | Data Table |  |
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| 26 | [SID847772] | Active | | | HTS for Tumor Hsp90 Inhibitors [AID429, Type: screening] | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS for Tumor Hsp90 Inhibitors | | AID | 429 | | BioAssay type | screening | | Target | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] | | PubMed | | | Data Table |  |
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| 27 | [SID847772] | Active | | | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase [AID1556, Type: screening] | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase | | AID | 1556 | | BioAssay type | screening | | Target | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] | | PubMed | | | Data Table |  |
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| 28 | [SID847772] | Active | | | HTS of Smad transcription factor inhibitors [AID630, Type: screening] | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS of Smad transcription factor inhibitors | | AID | 630 | | BioAssay type | screening | | Target | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] | | PubMed | | | Data Table |  |
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| 29 | [SID847772] | Active | | | HTS of Smad transcription factor inhibitors [AID630, Type: screening] | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS of Smad transcription factor inhibitors | | AID | 630 | | BioAssay type | screening | | Target | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] | | PubMed | | | Data Table |  |
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| 30 | [SID847772] | Active | | | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors [AID629, Type: screening] | Estrogen receptor 1 [Homo sapiens] [gi:118764400] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | | AID | 629 | | BioAssay type | screening | | Target | Estrogen receptor 1 [Homo sapiens] [gi:118764400] | | PubMed | | | Data Table |  |
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| 31 | [SID847772] | Active | | | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors [AID629, Type: screening] | Estrogen receptor 1 [Homo sapiens] [gi:118764400] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | | AID | 629 | | BioAssay type | screening | | Target | Estrogen receptor 1 [Homo sapiens] [gi:118764400] | | PubMed | | | Data Table |  |
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| 32 | [SID847772] | Active | | | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors [AID629, Type: screening] | Estrogen receptor 1 [Homo sapiens] [gi:118764400] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | | AID | 629 | | BioAssay type | screening | | Target | Estrogen receptor 1 [Homo sapiens] [gi:118764400] | | PubMed | | | Data Table |  |
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| 33 | [SID847772] | Active | | | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors [AID629, Type: screening] | Estrogen receptor 1 [Homo sapiens] [gi:118764400] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS of Estrogen Receptor- alpha Coactivator Binding inhibitors | | AID | 629 | | BioAssay type | screening | | Target | Estrogen receptor 1 [Homo sapiens] [gi:118764400] | | PubMed | | | Data Table |  |
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| 34 | [SID847772] | Active | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
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| 35 | [SID847772] | Active | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
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| 36 | [SID847772] | Active | | | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors [AID633, Type: screening] | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | | AID | 633 | | BioAssay type | screening | | Target | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] | | PubMed | | | Data Table |  |
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| 37 | [SID847772] | Active | | | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors [AID633, Type: screening] | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | | AID | 633 | | BioAssay type | screening | | Target | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] | | PubMed | | | Data Table |  |
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| 38 | [SID847772] | Active | | | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors [AID633, Type: screening] | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | HTS for Estrogen Receptor-beta Coactivator Binding inhibitors | | AID | 633 | | BioAssay type | screening | | Target | estrogen receptor beta isoform 1 [Homo sapiens] [gi:10835013] | | PubMed | | | Data Table |  |
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| 39 | [SID847772] | Active | | | uHTS Identification of Diaphorase Inhibitors and Chemcical Oxidizers: Counter Screen for Diaphorase-based Primary Assays [AID1217, Type: screening] | Dihydrolipoamide dehydrogenase [Homo sapiens] [gi:17391426] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | uHTS Identification of Diaphorase Inhibitors and Chemcical Oxidizers: Counter Screen for Diaphorase-based Primary Assays | | AID | 1217 | | BioAssay type | screening | | Target | Dihydrolipoamide dehydrogenase [Homo sapiens] [gi:17391426] | | PubMed | | | Data Table |  |
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| 40 | [SID847772] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_1, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 41 | [SID847772] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_1, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 42 | [SID847772] | Active | | | CYP2C19 Assay [AID778, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | CYP2C19 Assay | | AID | 778 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 43 | [SID847772] | Active | | | CYP2C19 Assay [AID778, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | CYP2C19 Assay | | AID | 778 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 44 | [SID847772] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_2, Type: other] | cytochrome P450, family 2, subfamily D, polypeptide 6 isoform 2 [Homo sapiens] [gi:68509921] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily D, polypeptide 6 isoform 2 [Homo sapiens] [gi:68509921] | | PubMed | | | Data Table |  |
|
| 45 | [SID847772] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_2, Type: other] | cytochrome P450, family 2, subfamily D, polypeptide 6 isoform 2 [Homo sapiens] [gi:68509921] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily D, polypeptide 6 isoform 2 [Homo sapiens] [gi:68509921] | | PubMed | | | Data Table |  |
|
| 46 | [SID847772] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_5, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 47 | [SID847772] | Active | | | Cytochrome panel assay with activity outcomes [AID1851_5, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 48 | [SID847772] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | CYP2C9 Assay | | AID | 777 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 49 | [SID847772] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | CYP2C9 Assay | | AID | 777 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 50 | [SID847772] | Active | | | CYP2C9 Assay [AID777, Type: screening] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 847772 | | CID | 6602529 | | Outcome | Active | | BioAssay | CYP2C9 Assay | | AID | 777 | | BioAssay type | screening | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|