| 1 | [SID4263567] | Active | IC50 | 0.28 | 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 | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 0.28 [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 |  |
|
| 2 | [SID4263567] | Active | IC50 | 0.28 | 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 | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 0.28 [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 |  |
|
| 3 | [SID4263567] | Active | IC50 | 0.28 | 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 | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 0.28 [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 |  |
|
| 4 | [SID4263567] | Active | IC50 | 0.997393 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 0.997393 [uM] | | BioAssay | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors | | AID | 1417 | | BioAssay type | confirmatory | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 5 | [SID4263567] | Active | IC50 | 0.997393 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 0.997393 [uM] | | BioAssay | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors | | AID | 1417 | | BioAssay type | confirmatory | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 6 | [SID4263567] | Active | IC50 | 0.997393 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 0.997393 [uM] | | BioAssay | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors | | AID | 1417 | | BioAssay type | confirmatory | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 7 | [SID4263567] | Active | IC50 | 1.0757 | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters [AID748, Type: confirmatory] | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 1.0757 [uM] | | BioAssay | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters | | AID | 748 | | BioAssay type | confirmatory | | Target | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] | | PubMed | | | Data Table |  |
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| 8 | [SID4263567] | Active | IC50 | 1.0757 | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters [AID748, Type: confirmatory] | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 1.0757 [uM] | | BioAssay | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters | | AID | 748 | | BioAssay type | confirmatory | | Target | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] | | PubMed | | | Data Table |  |
|
| 9 | [SID4263567] | Active | IC50 | 1.0757 | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters [AID748, Type: confirmatory] | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 1.0757 [uM] | | BioAssay | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters | | AID | 748 | | BioAssay type | confirmatory | | Target | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] | | PubMed | | | Data Table |  |
|
| 10 | [SID26513892] | Active | IC50 | 2.18 | In Vitro HePTP Dose Response Colorimetric Assay for SAR Study [AID1059, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 2.18 [uM] | | BioAssay | In Vitro HePTP Dose Response Colorimetric Assay for SAR Study | | AID | 1059 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
|
| 11 | [SID26513892] | Active | IC50 | 2.18 | In Vitro HePTP Dose Response Colorimetric Assay for SAR Study [AID1059, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 2.18 [uM] | | BioAssay | In Vitro HePTP Dose Response Colorimetric Assay for SAR Study | | AID | 1059 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
|
| 12 | [SID26513892] | Active | IC50 | 2.18 | In Vitro HePTP Dose Response Colorimetric Assay for SAR Study [AID1059, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 2.18 [uM] | | BioAssay | In Vitro HePTP Dose Response Colorimetric Assay for SAR Study | | AID | 1059 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 13 | [SID4263567] | Active | Potency | 3.1623 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 14 | [SID4263567] | Active | Potency | 3.1623 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 15 | [SID4263567] | Active | Potency | 3.1623 | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | | AID | 893 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
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| 16 | [SID4263567] | Active | Potency | 3.1623 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
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| 17 | [SID4263567] | Active | Potency | 3.9811 | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) [AID886, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 3.9811 [uM] | | BioAssay | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) | | AID | 886 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
|
| 18 | [SID4263567] | Active | Potency | 3.9811 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 3.9811 [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 |  |
|
| 19 | [SID4263567] | Active | Potency | 3.9811 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 3.9811 [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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| 20 | [SID4263567] | Active | IC50 | 4.11 | Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus [AID1419, Type: confirmatory] | BZLF2 [Human herpesvirus 4 type 2] [gi:139424501] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 4.11 [uM] | | BioAssay | Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus | | AID | 1419 | | BioAssay type | confirmatory | | Target | BZLF2 [Human herpesvirus 4 type 2] [gi:139424501] | | PubMed | | | Data Table |  |
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| 21 | [SID26513892] | Active | IC50 | 5.56 | In Vitro Hsp70 Dose Response Fluorescence Polarization Assay for SAR Study [AID1072, Type: confirmatory] | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 5.56 [uM] | | BioAssay | In Vitro Hsp70 Dose Response Fluorescence Polarization Assay for SAR Study | | AID | 1072 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] | | PubMed | | | Data Table |  |
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| 22 | [SID4263567] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 6.3096 [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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| 23 | [SID26513892] | Active | IC50 | 7.45 | Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP [AID1077, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 7.45 [uM] | | BioAssay | Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP | | AID | 1077 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
|
| 24 | [SID26513892] | Active | IC50 | 7.45 | Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP [AID1077, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 7.45 [uM] | | BioAssay | Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP | | AID | 1077 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
|
| 25 | [SID26513892] | Active | IC50 | 7.45 | Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP [AID1077, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 7.45 [uM] | | BioAssay | Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP | | AID | 1077 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
|
| 26 | [SID4263567] | Active | Potency | 7.9433 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | | AID | 485364 | | BioAssay type | confirmatory | | Target | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | | PubMed | | | Data Table |  |
|
| 27 | [SID4263567] | Active | Potency | 8.9125 | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2549, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2549 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
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| 28 | [SID26513892] | Active | IC50 | 9.873 | In Vitro MKP-3 Dose Response Assay for SAR Study [AID1055, Type: confirmatory] | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 9.873 [uM] | | BioAssay | In Vitro MKP-3 Dose Response Assay for SAR Study | | AID | 1055 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] | | PubMed | | | Data Table |  |
|
| 29 | [SID26513892] | Active | IC50 | 9.873 | In Vitro MKP-3 Dose Response Assay for SAR Study [AID1055, Type: confirmatory] | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 9.873 [uM] | | BioAssay | In Vitro MKP-3 Dose Response Assay for SAR Study | | AID | 1055 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] | | PubMed | | | Data Table |  |
|
| 30 | [SID26513892] | Active | IC50 | 9.873 | MKP-3 in vitro secondary assay for identification of redox-state modulating compounds [AID1054, Type: confirmatory] | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 9.873 [uM] | | BioAssay | MKP-3 in vitro secondary assay for identification of redox-state modulating compounds | | AID | 1054 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] | | PubMed | | | Data Table |  |
|
| 31 | [SID26513892] | Active | IC50 | 9.873 | MKP-3 in vitro secondary assay for identification of redox-state modulating compounds [AID1054, Type: confirmatory] | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 9.873 [uM] | | BioAssay | MKP-3 in vitro secondary assay for identification of redox-state modulating compounds | | AID | 1054 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] | | PubMed | | | Data Table |  |
|
| 32 | [SID4263567] | Active | IC50 | 10.2388 | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation [AID855, Type: confirmatory] | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 10.2388 [uM] | | BioAssay | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation | | AID | 855 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] | | PubMed | | | Data Table |  |
|
| 33 | [SID4263567] | Active | IC50 | 10.2388 | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation [AID855, Type: confirmatory] | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 10.2388 [uM] | | BioAssay | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation | | AID | 855 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] | | PubMed | | | Data Table |  |
|
| 34 | [SID4263567] | Active | IC50 | 14.2 | Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents [AID1903, Type: confirmatory] | large T antigen [Simian virus 40] [gi:297591903] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | IC50 | 14.2 [uM] | | BioAssay | Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents | | AID | 1903 | | BioAssay type | confirmatory | | Target | large T antigen [Simian virus 40] [gi:297591903] | | PubMed | | | Data Table |  |
|
| 35 | [SID26513892] | Active | IC50 | 14.7 | MKP-3 in vitro secondary assay for identification of irreversible and slow-binding inhibitors [AID1052, Type: confirmatory] | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 14.7 [uM] | | BioAssay | MKP-3 in vitro secondary assay for identification of irreversible and slow-binding inhibitors | | AID | 1052 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] | | PubMed | | | Data Table |  |
|
| 36 | [SID26513892] | Active | IC50 | 14.7 | MKP-3 in vitro secondary assay for identification of irreversible and slow-binding inhibitors [AID1052, Type: confirmatory] | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 14.7 [uM] | | BioAssay | MKP-3 in vitro secondary assay for identification of irreversible and slow-binding inhibitors | | AID | 1052 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 6 [Rattus norvegicus] [gi:16758752] | | PubMed | | | Data Table |  |
|
| 37 | [SID4263567] | Active | Potency | 15.8489 | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
|
| 38 | [SID4263567] | Active | Potency | 15.8489 | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
|
| 39 | [SID4263567] | Active | Potency | 15.8489 | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
|
| 40 | [SID4263567] | Active | Potency | 17.7828 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 41 | [SID4263567] | Active | Potency | 17.7828 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 42 | [SID4263567] | Active | Potency | 19.0115 | qHTS Assay to Find Inhibitors of T. brucei phosphofructokinase [AID485367, Type: confirmatory] | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 19.0115 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of T. brucei phosphofructokinase | | AID | 485367 | | BioAssay type | confirmatory | | Target | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] | | PubMed | | | Data Table |  |
|
| 43 | [SID4263567] | Active | Potency | 19.9526 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 44 | [SID4263567] | Active | Potency | 19.9526 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 45 | [SID4263567] | Active | Potency | 25.1189 | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2517, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2517 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
|
| 46 | [SID26513892] | Active | IC50 | 27 | In Vitro Hsc70 Dose Response Fluorescence Polarization Assay [AID1193, Type: confirmatory] | heat shock cognate 71 kDa protein isoform 1 [Homo sapiens] [gi:5729877] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 27 [uM] | | BioAssay | In Vitro Hsc70 Dose Response Fluorescence Polarization Assay | | AID | 1193 | | BioAssay type | confirmatory | | Target | heat shock cognate 71 kDa protein isoform 1 [Homo sapiens] [gi:5729877] | | PubMed | | | Data Table |  |
|
| 47 | [SID26513892] | Active | IC50 | 27 | In Vitro Hsc70 Dose Response Fluorescence Polarization Assay [AID1193, Type: confirmatory] | heat shock cognate 71 kDa protein isoform 1 [Homo sapiens] [gi:5729877] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 27 [uM] | | BioAssay | In Vitro Hsc70 Dose Response Fluorescence Polarization Assay | | AID | 1193 | | BioAssay type | confirmatory | | Target | heat shock cognate 71 kDa protein isoform 1 [Homo sapiens] [gi:5729877] | | PubMed | | | Data Table |  |
|
| 48 | [SID26513892] | Active | IC50 | 27 | In Vitro Hsc70 Dose Response Fluorescence Polarization Assay [AID1193, Type: confirmatory] | heat shock cognate 71 kDa protein isoform 1 [Homo sapiens] [gi:5729877] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 27 [uM] | | BioAssay | In Vitro Hsc70 Dose Response Fluorescence Polarization Assay | | AID | 1193 | | BioAssay type | confirmatory | | Target | heat shock cognate 71 kDa protein isoform 1 [Homo sapiens] [gi:5729877] | | PubMed | | | Data Table |  |
|
| 49 | [SID4263567] | Active | Potency | 28.1838 | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 4263567 | | CID | 2859888 | | Outcome | Active | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | | AID | 2528 | | BioAssay type | confirmatory | | Target | Bloom syndrome protein [Homo sapiens] [gi:4557365] | | PubMed | | | Data Table |  |
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| 50 | [SID26513892] | Active | IC50 | 95.4 | GAPDH Dose Response Colorimetric Assay [AID1227, Type: confirmatory] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 26513892 | | CID | 2859888 | | Outcome | Active | | IC50 | 95.4 [uM] | | BioAssay | GAPDH Dose Response Colorimetric Assay | | AID | 1227 | | BioAssay type | confirmatory | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
|