| 1 | [SID125317282] | Active | IC50 | 0.858 | SAR analysis of small molecule inhibitors of APOBEC3G DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 [AID624087, Type: confirmatory] | APOBEC3G gene product [Homo sapiens] [gi:13399304] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 125317282 | | CID | 646406 | | Outcome | Active | | IC50 | 0.858 [uM] | | BioAssay | SAR analysis of small molecule inhibitors of APOBEC3G DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 | | AID | 624087 | | BioAssay type | confirmatory | | Target | APOBEC3G gene product [Homo sapiens] [gi:13399304] | | PubMed | | | Data Table |  |
|
| 2 | [SID125317282] | Active | IC50 | 1.7 | SAR analysis of small molecule inhibitors of APOBEC3A DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 [AID624089, Type: confirmatory] | APOBEC3A gene product [Homo sapiens] [gi:21955158] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 125317282 | | CID | 646406 | | Outcome | Active | | IC50 | 1.7 [uM] | | BioAssay | SAR analysis of small molecule inhibitors of APOBEC3A DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 | | AID | 624089 | | BioAssay type | confirmatory | | Target | APOBEC3A gene product [Homo sapiens] [gi:21955158] | | PubMed | | | Data Table |  |
|
| 3 | [SID844096] | Active | IC50 | 1.8894 | 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. | 3 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 1.8894 [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 |  |
|
| 4 | [SID844096] | Active | IC50 | 1.8894 | 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. | 4 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 1.8894 [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 |  |
|
| 5 | [SID844096] | Active | IC50 | 1.8894 | 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. | 5 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 1.8894 [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 |  |
|
| 6 | [SID844096] | Active | IC50 | 2.12 | 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. | 6 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 2.12 [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 |  |
|
| 7 | [SID844096] | Active | IC50 | 2.12 | 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. | 7 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 2.12 [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 |  |
|
| 8 | [SID844096] | Active | IC50 | 2.12 | 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. | 8 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 2.12 [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 |  |
|
| 9 | [SID844096] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 10 | [SID844096] | Active | Potency | 2.5119 | 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 | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 11 | [SID844096] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 12 | [SID844096] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 13 | [SID26667401] | Active | Potency | 2.5119 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 26667401 | | CID | 646406 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 14 | [SID844096] | Active | Potency | 2.5119 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 15 | [SID844096] | Active | Potency | 3.1623 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 16 | [SID844096] | Active | Potency | 3.1623 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 17 | [SID26667401] | Active | Potency | 3.1623 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 26667401 | | CID | 646406 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 18 | [SID26667401] | Active | Potency | 3.1623 | 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 | 26667401 | | CID | 646406 | | Outcome | Active | | Potency | 3.1623 [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 | [SID26667401] | Active | IC50 | 3.17049 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 26667401 | | CID | 646406 | | Outcome | Active | | IC50 | 3.17049 [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 |  |
|
| 20 | [SID26667401] | Active | IC50 | 3.17049 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26667401 | | CID | 646406 | | Outcome | Active | | IC50 | 3.17049 [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 |  |
|
| 21 | [SID26667401] | Active | IC50 | 3.17049 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26667401 | | CID | 646406 | | Outcome | Active | | IC50 | 3.17049 [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 |  |
|
| 22 | [SID844096] | Active | Potency | 3.5481 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 3.5481 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 23 | [SID844096] | Active | Potency | 3.5481 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 3.5481 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 24 | [SID26667401] | Active | Potency | 3.5481 | 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. | 24 | | Structure |
| | Substance | | | SID | 26667401 | | CID | 646406 | | Outcome | Active | | Potency | 3.5481 [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 |  |
|
| 25 | [SID844096] | Active | Potency | 3.9811 | 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. | 25 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 3.9811 [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 |  |
|
| 26 | [SID26514186] | Active | IC50 | 4.81 | 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. | 26 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 4.81 [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 |  |
|
| 27 | [SID26514186] | Active | IC50 | 4.81 | 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. | 27 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 4.81 [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 |  |
|
| 28 | [SID26514186] | Active | IC50 | 4.81 | 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. | 28 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 4.81 [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 |  |
|
| 29 | [SID844096] | Active | Potency | 5.0119 | 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. | 29 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 5.0119 [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 |  |
|
| 30 | [SID844096] | Active | Potency | 5.0119 | 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. | 30 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 5.0119 [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 |  |
|
| 31 | [SID844096] | Active | Potency | 5.0119 | 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. | 31 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 5.0119 [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 |  |
|
| 32 | [SID26514186] | Active | IC50 | 5.43 | 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. | 32 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 5.43 [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 |  |
|
| 33 | [SID26514186] | Active | IC50 | 5.43 | 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. | 33 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 5.43 [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 |  |
|
| 34 | [SID26514186] | Active | IC50 | 5.43 | 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. | 34 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 5.43 [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 |  |
|
| 35 | [SID26514186] | Active | IC50 | 5.963 | 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. | 35 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 5.963 [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 |  |
|
| 36 | [SID26514186] | Active | IC50 | 5.963 | 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. | 36 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 5.963 [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 |  |
|
| 37 | [SID26514186] | Active | IC50 | 5.963 | 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. | 37 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 5.963 [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 |  |
|
| 38 | [SID26514186] | Active | IC50 | 5.963 | 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. | 38 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 5.963 [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 |  |
|
| 39 | [SID26514186] | Active | IC50 | 6.2 | 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. | 39 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 6.2 [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 |  |
|
| 40 | [SID26514186] | Active | IC50 | 6.2 | 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. | 40 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 6.2 [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 |  |
|
| 41 | [SID125317282] | Active | IC50 | 6.55 | SAR analysis of small molecule inhibitors of APOBEC3A DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay [AID588857, Type: confirmatory] | APOBEC3A gene product [Homo sapiens] [gi:21955158] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 125317282 | | CID | 646406 | | Outcome | Active | | IC50 | 6.55 [uM] | | BioAssay | SAR analysis of small molecule inhibitors of APOBEC3A DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay | | AID | 588857 | | BioAssay type | confirmatory | | Target | APOBEC3A gene product [Homo sapiens] [gi:21955158] | | PubMed | | | Data Table |  |
|
| 42 | [SID844096] | Active | Potency | 7.0795 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 7.0795 [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 |  |
|
| 43 | [SID844096] | Active | Potency | 7.0795 | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation with Orthogonal Assay [AID504375, Type: confirmatory] | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation with Orthogonal Assay | | AID | 504375 | | BioAssay type | confirmatory | | Target | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] | | PubMed | | | Data Table |  |
|
| 44 | [SID844096] | Active | Potency | 7.0795 | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation with Orthogonal Assay [AID504375, Type: confirmatory] | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation with Orthogonal Assay | | AID | 504375 | | BioAssay type | confirmatory | | Target | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] | | PubMed | | | Data Table |  |
|
| 45 | [SID26514186] | Active | IC50 | 7.18 | 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. | 45 | | Structure |
| | Substance | | | SID | 26514186 | | CID | 646406 | | Outcome | Active | | IC50 | 7.18 [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 |  |
|
| 46 | [SID844096] | Active | Potency | 7.5686 | qHTS Assay to Find Inhibitors of Pin1 [AID504891, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 7.5686 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Pin1 | | AID | 504891 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
|
| 47 | [SID844096] | Active | Potency | 7.5686 | qHTS Assay to Find Inhibitors of Pin1 [AID504891, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 7.5686 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Pin1 | | AID | 504891 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
|
| 48 | [SID844096] | Active | Potency | 7.9433 | 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. | 48 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | Potency | 7.9433 [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 |  |
|
| 49 | [SID844096] | Active | IC50 | 8.68313 | 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. | 49 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 8.68313 [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 |  |
|
| 50 | [SID844096] | Active | IC50 | 8.68313 | 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. | 50 | | Structure |
| | Substance | | | SID | 844096 | | CID | 646406 | | Outcome | Active | | IC50 | 8.68313 [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 |  |
|