| 1 | [SID26749198] | Active | Potency | 0.3162 | 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. | 1 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 0.3162 [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 |  |
|
| 2 | [SID26753750] | Active | Potency | 0.631 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 0.631 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 3 | [SID26753750] | Active | Potency | 0.631 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 0.631 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
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| 4 | [SID26749198] | Active | Potency | 0.7943 | 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. | 4 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 0.7943 [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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| 5 | [SID103222861] | Active | IC50 | 0.8 | Antiproliferative (inhibition of cell growth) activity against HaCaT cells (human keratinocyte line) [AID85482, Type: Literature] | |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 0.8 [uM] | | BioAssay | Antiproliferative (inhibition of cell growth) activity against HaCaT cells (human keratinocyte line) | | AID | 85482 | | BioAssay type | Literature | | Target | | | PubMed | 9371243 | | Data Table |  |
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| 6 | [SID103222861] | Active | IC50 | 1 | Inhibition of purified human recombinant IDO [AID326467, Type: Literature] | Indoleamine 2,3-dioxygenase 1 [gi:123948] |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 1 [uM] | | BioAssay | Inhibition of purified human recombinant IDO | | AID | 326467 | | BioAssay type | Literature | | Target | Indoleamine 2,3-dioxygenase 1 [gi:123948] | | PubMed | 18318466 | | Data Table |  |
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| 7 | [SID103222861] | Active | IC50 | 1.4 | Antiproliferative activity against human A2780 cells after 2 days by alamar-blue assay [AID417089, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 1.4 [uM] | | BioAssay | Antiproliferative activity against human A2780 cells after 2 days by alamar-blue assay | | AID | 417089 | | BioAssay type | Literature | | Target | | | PubMed | 19028102 | | Data Table |  |
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| 8 | [SID26749198] | Active | Potency | 1.7783 | 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. | 8 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 1.7783 [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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| 9 | [SID103222861] | Active | IC50 | 1.98 | Inhibition of histidine-tagged human recombinant Cdc25B catalytic domain expressed in Escherichia coli [AID417086, Type: Literature] | M-phase inducer phosphatase 2 [gi:21264471] |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 1.98 [uM] | | BioAssay | Inhibition of histidine-tagged human recombinant Cdc25B catalytic domain expressed in Escherichia coli | | AID | 417086 | | BioAssay type | Literature | | Target | M-phase inducer phosphatase 2 [gi:21264471] | | PubMed | 19028102 | | Data Table |  |
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| 10 | [SID103222861] | Active | IC50 | 1.98 | Inhibition of histidine-tagged human recombinant Cdc25B catalytic domain expressed in Escherichia coli [AID417086, Type: Literature] | M-phase inducer phosphatase 2 [gi:21264471] |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 1.98 [uM] | | BioAssay | Inhibition of histidine-tagged human recombinant Cdc25B catalytic domain expressed in Escherichia coli | | AID | 417086 | | BioAssay type | Literature | | Target | M-phase inducer phosphatase 2 [gi:21264471] | | PubMed | 19028102 | | Data Table |  |
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| 11 | [SID26749198] | Active | Potency | 1.9953 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 1.9953 [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | | AID | 887 | | BioAssay type | confirmatory | | Target | 15-lipoxygenase [Homo sapiens] [gi:1832253] | | PubMed | | | Data Table |  |
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| 12 | [SID26749198] | Active | Potency | 1.9953 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 1.9953 [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | | AID | 887 | | BioAssay type | confirmatory | | Target | 15-lipoxygenase [Homo sapiens] [gi:1832253] | | PubMed | | | Data Table |  |
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| 13 | [SID26753750] | Active | Potency | 1.9953 | 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. | 13 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 1.9953 [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 |  |
|
| 14 | [SID26749198] | Active | Potency | 2.2387 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 15 | [SID26749198] | Active | Potency | 2.2387 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 16 | [SID26753750] | Active | Potency | 2.6679 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 2.6679 [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 | [SID26753750] | Active | Potency | 2.6679 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 2.6679 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 18 | [SID26749198] | Active | Potency | 3.1623 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | 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 |  |
|
| 19 | [SID26749198] | Active | Potency | 3.1623 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | 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 |  |
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| 20 | [SID26749198] | Active | Potency | 3.1623 | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) [AID881, Type: confirmatory] | Arachidonate 15-lipoxygenase B [gi:317373425] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) | | AID | 881 | | BioAssay type | confirmatory | | Target | Arachidonate 15-lipoxygenase B [gi:317373425] | | PubMed | | | Data Table |  |
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| 21 | [SID26749198] | Active | Potency | 3.1623 | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 3.1623 [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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| 22 | [SID103222861] | Active | IC50 | 3.7 | In vitro antimalarial activity against human malaria parasite, P falciparum (Vietnam Smith strain) [AID152094, Type: Literature] | |   View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 3.7 [uM] | | BioAssay | In vitro antimalarial activity against human malaria parasite, P falciparum (Vietnam Smith strain) | | AID | 152094 | | BioAssay type | Literature | | Target | | | PubMed | 2033589 | | Data Table |  |
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| 23 | [SID26753750] | Active | Potency | 4.4668 | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation [AID504374, Type: confirmatory] | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 4.4668 [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation | | AID | 504374 | | BioAssay type | confirmatory | | Target | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] | | PubMed | | | Data Table |  |
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| 24 | [SID26753750] | Active | Potency | 4.4668 | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation [AID504374, Type: confirmatory] | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 4.4668 [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia: Hit Validation | | AID | 504374 | | BioAssay type | confirmatory | | Target | core-binding factor subunit beta isoform 2 [Homo sapiens] [gi:13124873] | | PubMed | | | Data Table |  |
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| 25 | [SID26753750] | Active | Potency | 4.4668 | 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. | 25 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 4.4668 [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 |  |
|
| 26 | [SID103222861] | Active | MIC | 5 | Inhibition of topoisomerase I [AID228426, Type: Literature] | |   View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | MIC | 5 [uM] | | BioAssay | Inhibition of topoisomerase I | | AID | 228426 | | BioAssay type | Literature | | Target | | | PubMed | 9873739 | | Data Table |  |
|
| 27 | [SID26753750] | Active | Potency | 5.6234 | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 5.6234 [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 |  |
|
| 28 | [SID26749198] | Active | Potency | 7.0795 | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) [AID2147, Type: confirmatory] | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) | | AID | 2147 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] | | PubMed | | | Data Table |  |
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| 29 | [SID26749198] | Active | Potency | 7.0795 | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 7.0795 [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 30 | [SID26749198] | Active | Potency | 7.9433 | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent) [AID1476, Type: confirmatory] | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent) | | AID | 1476 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] | | PubMed | | | Data Table |  |
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| 31 | [SID26749198] | Active | Potency | 7.9433 | Confirmation qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2708, 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 | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2708 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
|
| 32 | [SID26749198] | Active | Potency | 8.9125 | Inhibitors of USP1/UAF1: Pilot qHTS [AID504865, Type: confirmatory] | USP1 protein [Homo sapiens] [gi:118600387] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | Inhibitors of USP1/UAF1: Pilot qHTS | | AID | 504865 | | BioAssay type | confirmatory | | Target | USP1 protein [Homo sapiens] [gi:118600387] | | PubMed | | | Data Table |  |
|
| 33 | [SID26753750] | Active | Potency | 8.9125 | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
|
| 34 | [SID26753750] | Active | Potency | 8.9125 | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
|
| 35 | [SID26753750] | Active | Potency | 8.9125 | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 26753750 | | CID | 3806 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
|
| 36 | [SID26749198] | Active | Potency | 10 | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
|
| 37 | [SID26749198] | Active | Potency | 10 | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
|
| 38 | [SID26749198] | Active | Potency | 10 | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
|
| 39 | [SID26749198] | Active | Potency | 11.2202 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 40 | [SID26749198] | Active | Potency | 11.2202 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 41 | [SID103222861] | Active | IC50 | 12.4 | Inhibition of histidine-tagged rat recombinant MKP3 catalytic domain expressed in Escherichia coli BL21(DE3) [AID417088, Type: Literature] | Dual specificity protein phosphatase 6 [gi:2499748] |   View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 12.4 [uM] | | BioAssay | Inhibition of histidine-tagged rat recombinant MKP3 catalytic domain expressed in Escherichia coli BL21(DE3) | | AID | 417088 | | BioAssay type | Literature | | Target | Dual specificity protein phosphatase 6 [gi:2499748] | | PubMed | 19028102 | | Data Table |  |
|
| 42 | [SID103222861] | Active | IC50 | 12.4 | Inhibition of histidine-tagged rat recombinant MKP3 catalytic domain expressed in Escherichia coli BL21(DE3) [AID417088, Type: Literature] | Dual specificity protein phosphatase 6 [gi:2499748] |   View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 12.4 [uM] | | BioAssay | Inhibition of histidine-tagged rat recombinant MKP3 catalytic domain expressed in Escherichia coli BL21(DE3) | | AID | 417088 | | BioAssay type | Literature | | Target | Dual specificity protein phosphatase 6 [gi:2499748] | | PubMed | 19028102 | | Data Table |  |
|
| 43 | [SID26749198] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a [AID927, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a | | AID | 927 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 44 | [SID26749198] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a [AID927, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a | | AID | 927 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 45 | [SID26749198] | Active | Potency | 12.5893 | 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. | 45 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 46 | [SID26749198] | Active | Potency | 12.5893 | 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. | 46 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 47 | [SID103222861] | Active | IC50 | 13 | Inhibition of histidine-tagged mouse MKP1 catalytic domain expressed in human Hela cells [AID417087, Type: Literature] | Dual specificity protein phosphatase 1 [gi:136027] |   View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 103222861 | | CID | 3806 | | Outcome | Active | | IC50 | 13 [uM] | | BioAssay | Inhibition of histidine-tagged mouse MKP1 catalytic domain expressed in human Hela cells | | AID | 417087 | | BioAssay type | Literature | | Target | Dual specificity protein phosphatase 1 [gi:136027] | | PubMed | 19028102 | | Data Table |  |
|
| 48 | [SID26749198] | Active | Potency | 14.1254 | 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. | 48 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 14.1254 [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 |  |
|
| 49 | [SID26749198] | Active | Potency | 14.1254 | 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. | 49 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 14.1254 [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 |  |
|
| 50 | [SID26749198] | Active | Potency | 14.1254 | 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. | 50 | | Structure |
| | Substance | | | SID | 26749198 | | CID | 3806 | | Outcome | Active | | Potency | 14.1254 [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 |  |
|