| 1 | [SID103178961] | Active | IC50 | 0.0047 | Concentration required to inhibit production of LTC4 from THP-1 cells stimulated with A-23187 [AID209196, Type: Literature] | |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | IC50 | 0.0047 [uM] | | BioAssay | Concentration required to inhibit production of LTC4 from THP-1 cells stimulated with A-23187 | | AID | 209196 | | BioAssay type | Literature | | Target | | | PubMed | 11229777 | | Data Table |  |
|
| 2 | [SID26747902] | Active | Potency | 0.0794 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 0.0794 [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 |  |
|
| 3 | [SID26747902] | Active | Potency | 0.0794 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 0.0794 [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 |  |
|
| 4 | [SID103178961] | Active | IC50 | 0.18 | Concentration required to inhibit production of PGE-2 from THP-1 cells stimulated with A-23187 [AID209197, Type: Literature] | |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | IC50 | 0.18 [uM] | | BioAssay | Concentration required to inhibit production of PGE-2 from THP-1 cells stimulated with A-23187 | | AID | 209197 | | BioAssay type | Literature | | Target | | | PubMed | 11229777 | | Data Table |  |
|
| 5 | [SID103178961] | Active | Kd | 0.18 | Binding affinity against Adipocyte lipid binding protein [AID32788, Type: Literature] | |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | Kd | 0.18 [uM] | | BioAssay | Binding affinity against Adipocyte lipid binding protein | | AID | 32788 | | BioAssay type | Literature | | Target | | | PubMed | 12036355 | | Data Table |  |
|
| 6 | [SID103178961] | Active | IC50 | 0.3 | Inhibition of mPGES1 [AID405533, Type: Literature] | |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | IC50 | 0.3 [uM] | | BioAssay | Inhibition of mPGES1 | | AID | 405533 | | BioAssay type | Literature | | Target | | | PubMed | 18459759 | | Data Table |  |
|
| 7 | [SID26753719] | Active | Potency | 0.3162 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 0.3162 [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 |  |
|
| 8 | [SID26753719] | Active | Potency | 0.3162 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 0.3162 [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 |  |
|
| 9 | [SID103178961] | Active | IC50 | 0.94 | Concentration required to inhibit production of LTB4 from whole blood stimulated with A-23187 [AID223075, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | IC50 | 0.94 [uM] | | BioAssay | Concentration required to inhibit production of LTB4 from whole blood stimulated with A-23187 | | AID | 223075 | | BioAssay type | Literature | | Target | | | PubMed | 11229777 | | Data Table |  |
|
| 10 | [SID103178961] | Active | Km | 1 | Activity of COX2 [AID336480, Type: Literature] | |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | Km | 1 [uM] | | BioAssay | Activity of COX2 | | AID | 336480 | | BioAssay type | Literature | | Target | | | PubMed | 12444669 | | Data Table |  |
|
| 11 | [SID26753719] | Active | Potency | 1.9953 | 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. | 11 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 1.9953 [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 |  |
|
| 12 | [SID26747902] | Active | Potency | 2.2387 | 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. | 12 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 2.2387 [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 |  |
|
| 13 | [SID26747902] | Active | Potency | 2.8184 | 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. | 13 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 2.8184 [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 |  |
|
| 14 | [SID26747902] | Active | Potency | 2.8184 | 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. | 14 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 2.8184 [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 |  |
|
| 15 | [SID26747902] | Active | Potency | 3.9811 | 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 | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 3.9811 [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 |  |
|
| 16 | [SID26747902] | Active | Potency | 5.6234 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 5.6234 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 17 | [SID26747902] | Active | Potency | 5.6234 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 5.6234 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 18 | [SID26747902] | Active | Potency | 5.6234 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 5.6234 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 19 | [SID26747902] | Active | Potency | 5.6234 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 5.6234 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 20 | [SID26753719] | Active | Potency | 7.9433 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 21 | [SID26753719] | Active | Potency | 7.9433 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 22 | [SID26753719] | Active | Potency | 7.9433 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 23 | [SID26753719] | Active | Potency | 7.9433 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 24 | [SID26753719] | Active | Potency | 7.9433 | 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. | 24 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 7.9433 [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 |  |
|
| 25 | [SID26753719] | Active | Potency | 7.9433 | 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. | 25 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 7.9433 [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 |  |
|
| 26 | [SID103178961] | Active | Km | 8.8 | Activity of bovine seminal microsomal COX1 [AID399408, Type: Literature] | Prostaglandin G/H synthase 1 [gi:166897622] |   View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | Km | 8.8 [uM] | | BioAssay | Activity of bovine seminal microsomal COX1 | | AID | 399408 | | BioAssay type | Literature | | Target | Prostaglandin G/H synthase 1 [gi:166897622] | | PubMed | 9461646 | | Data Table |  |
|
| 27 | [SID103178961] | Active | Km | 9.7 | Activity of sheep placental cotyledons COX2 [AID399409, Type: Literature] | Prostaglandin G/H synthase 2 [gi:3914304] |   View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | Km | 9.7 [uM] | | BioAssay | Activity of sheep placental cotyledons COX2 | | AID | 399409 | | BioAssay type | Literature | | Target | Prostaglandin G/H synthase 2 [gi:3914304] | | PubMed | 9461646 | | Data Table |  |
|
| 28 | [SID103178961] | Active | IC50 | 10 | Inhibition of hepatitis C virus replication in Huh7-K2040 cells in presence of delipidated fetal calf serum medium by RT-PCR [AID330323, Type: Literature] | |   View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | IC50 | 10 [uM] | | BioAssay | Inhibition of hepatitis C virus replication in Huh7-K2040 cells in presence of delipidated fetal calf serum medium by RT-PCR | | AID | 330323 | | BioAssay type | Literature | | Target | | | PubMed | 18003907 | | Data Table |  |
|
| 29 | [SID26747902] | Active | Potency | 11.5821 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 11.5821 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 30 | [SID26747902] | Active | Potency | 11.5821 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 11.5821 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 31 | [SID26747902] | Active | Potency | 11.5821 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 11.5821 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 32 | [SID26753719] | Active | Potency | 12.5893 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 33 | [SID26753719] | Active | Potency | 12.5893 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 34 | [SID26747902] | Active | Potency | 12.5893 | 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. | 34 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 35 | [SID26747902] | Active | Potency | 12.5893 | 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. | 35 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 36 | [SID103178961] | Active | Km | 15 | Activity of soybean lipooxygenase 1 [AID409935, Type: Literature] | |   View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | Km | 15 [uM] | | BioAssay | Activity of soybean lipooxygenase 1 | | AID | 409935 | | BioAssay type | Literature | | Target | | | PubMed | 18793849 | | Data Table |  |
|
| 37 | [SID57261284] | Active | Potency | 15.8489 | 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. | 37 | | Structure |
| | Substance | | | SID | 57261284 | | CID | 444899 | | Outcome | Active | | Potency | 15.8489 [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 |  |
|
| 38 | [SID26747902] | 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 | 26747902 | | CID | 444899 | | 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 | [SID26747902] | 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 | 26747902 | | CID | 444899 | | 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 |  |
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| 40 | [SID26747902] | 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. | 40 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | 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 |  |
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| 41 | [SID26747902] | Active | Potency | 15.8489 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 15.8489 [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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| 42 | [SID26747902] | Active | Potency | 15.8489 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 15.8489 [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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| 43 | [SID57261284] | Active | Potency | 17.7828 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 57261284 | | CID | 444899 | | Outcome | Active | | Potency | 17.7828 [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 |  |
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| 44 | [SID103178961] | Active | EC50 | 22.1 | Antiviral activity against HCV assessed as inhibition of HCV RNA replication in OR6 cells after 72 hrs by luciferase reporter assay [AID323922, Type: Literature] | |   View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103178961 | | CID | 444899 | | Outcome | Active | | EC50 | 22.1 [uM] | | BioAssay | Antiviral activity against HCV assessed as inhibition of HCV RNA replication in OR6 cells after 72 hrs by luciferase reporter assay | | AID | 323922 | | BioAssay type | Literature | | Target | | | PubMed | 17420205 | | Data Table |  |
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| 45 | [SID26747902] | Active | Potency | 22.3872 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 22.3872 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
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| 46 | [SID26747902] | Active | Potency | 22.3872 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 22.3872 [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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| 47 | [SID26747902] | Active | Potency | 22.3872 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 26747902 | | CID | 444899 | | Outcome | Active | | Potency | 22.3872 [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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| 48 | [SID26753719] | Active | Potency | 23.715 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 23.715 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 49 | [SID26753719] | Active | Potency | 23.715 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 23.715 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 50 | [SID26753719] | Active | Potency | 23.715 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 26753719 | | CID | 444899 | | Outcome | Active | | Potency | 23.715 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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