| 1 | [SID11111541] | Active | Potency | 0.1259 | 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. | 1 | | Structure |
| | Substance | | | SID | 11111541 | | CID | 71398 | | Outcome | Active | | Potency | 0.1259 [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 |  |
|
| 2 | [SID50106727] | Active | Potency | 0.1585 | 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. | 2 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 0.1585 [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 |  |
|
| 3 | [SID50106727] | Active | Potency | 0.1585 | 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. | 3 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 0.1585 [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 |  |
|
| 4 | [SID11111540] | Active | Potency | 0.631 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 0.631 [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 |  |
|
| 5 | [SID11111540] | Active | Potency | 0.631 | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 0.631 [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 |  |
|
| 6 | [SID90341429] | Active | Potency | 0.631 | qHTS for Inhibitors of Glutaminase (GLS): LOPAC Validation [AID624146, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 0.631 [uM] | | BioAssay | qHTS for Inhibitors of Glutaminase (GLS): LOPAC Validation | | AID | 624146 | | BioAssay type | confirmatory | | Target | GLS protein [Homo sapiens] [gi:71051501] | | PubMed | | | Data Table |  |
|
| 7 | [SID90341429] | Active | Potency | 0.7519 | qHTS Validation Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1) [AID488816, Type: confirmatory] | flap endonuclease 1 [Homo sapiens] [gi:4758356] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 0.7519 [uM] | | BioAssay | qHTS Validation Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1) | | AID | 488816 | | BioAssay type | confirmatory | | Target | flap endonuclease 1 [Homo sapiens] [gi:4758356] | | PubMed | | | Data Table |  |
|
| 8 | [SID90341429] | Active | Potency | 0.7519 | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). [AID588795, Type: confirmatory] | flap endonuclease 1 [Homo sapiens] [gi:4758356] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 0.7519 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). | | AID | 588795 | | BioAssay type | confirmatory | | Target | flap endonuclease 1 [Homo sapiens] [gi:4758356] | | PubMed | | | Data Table |  |
|
| 9 | [SID90341429] | Active | Potency | 0.7943 | 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. | 9 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 0.7943 [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 |  |
|
| 10 | [SID50106727] | Active | Potency | 0.7943 | 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 | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 0.7943 [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 | [SID50106727] | Active | Potency | 0.7943 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 0.7943 [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 |  |
|
| 12 | [SID11111540] | Active | Potency | 1 | 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. | 12 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 1 [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 |  |
|
| 13 | [SID50106727] | Active | Potency | 1.2589 | Confirmation qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID2157, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 1.2589 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | | AID | 2157 | | BioAssay type | confirmatory | | Target | 15-lipoxygenase [Homo sapiens] [gi:1832253] | | PubMed | | | Data Table |  |
|
| 14 | [SID50106727] | Active | Potency | 1.2589 | Confirmation qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID2157, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 1.2589 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | | AID | 2157 | | BioAssay type | confirmatory | | Target | 15-lipoxygenase [Homo sapiens] [gi:1832253] | | PubMed | | | Data Table |  |
|
| 15 | [SID50106727] | Active | Potency | 1.2589 | Confirmation qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) [AID2537, Type: confirmatory] | Arachidonate 15-lipoxygenase B [gi:317373425] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 1.2589 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) | | AID | 2537 | | BioAssay type | confirmatory | | Target | Arachidonate 15-lipoxygenase B [gi:317373425] | | PubMed | | | Data Table |  |
|
| 16 | [SID11111541] | Active | Potency | 1.5849 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 [AID883, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 11111541 | | CID | 71398 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 | | AID | 883 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 17 | [SID11111541] | Active | Potency | 1.5849 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 [AID883, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 11111541 | | CID | 71398 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 | | AID | 883 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 18 | [SID11111541] | Active | Potency | 1.5849 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 [AID883, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 11111541 | | CID | 71398 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 | | AID | 883 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 19 | [SID90341429] | Active | Potency | 1.6834 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 1.6834 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 20 | [SID90341429] | Active | Potency | 1.6834 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 1.6834 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 21 | [SID50106727] | Active | Potency | 1.7783 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 1.7783 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
|
| 22 | [SID50106727] | Active | Potency | 1.7783 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 1.7783 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
|
| 23 | [SID50106727] | Active | Potency | 2.2387 | Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1): Followup Confirmation and Counterscreen [AID493210, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1): Followup Confirmation and Counterscreen | | AID | 493210 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 24 | [SID50106727] | Active | Potency | 2.2387 | Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1): Followup Confirmation and Counterscreen [AID493210, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1): Followup Confirmation and Counterscreen | | AID | 493210 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 25 | [SID50106727] | Active | Potency | 2.5119 | 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 | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 2.5119 [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 | [SID11111540] | Active | Potency | 2.5119 | 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. | 26 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 27 | [SID11111540] | 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. | 27 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | 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 |  |
|
| 28 | [SID50106727] | Active | Potency | 3.1623 | 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. | 28 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 29 | [SID50106727] | Active | Potency | 3.1623 | 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. | 29 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 30 | [SID50106727] | Active | Potency | 3.1623 | 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. | 30 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 31 | [SID50106727] | Active | Potency | 3.1623 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 32 | [SID50106727] | Active | Potency | 3.1623 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 33 | [SID50106727] | Active | Potency | 3.9811 | 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. | 33 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 3.9811 [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 |  |
|
| 34 | [SID50106727] | Active | Potency | 3.9811 | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line 7G8 [AID1815, Type: confirmatory] | |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 3.9811 [uM] | | BioAssay | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line 7G8 | | AID | 1815 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 35 | [SID50106727] | Active | Potency | 5.0119 | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line GB4 [AID1816, Type: confirmatory] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line GB4 | | AID | 1816 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 36 | [SID124891671] | Active | Potency | 5.0119 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 124891671 | | CID | 71398 | | Outcome | Active | | Potency | 5.0119 [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 | | | PubMed | | | Data Table |  |
|
| 37 | [SID11111540] | Active | Potency | 5.0119 | qHTS Assay for Identification of Small Molecule Antagonists for Thrombopoietin (TPO) Signaling Pathway [AID918, Type: confirmatory] | Thrombopoietin [Homo sapiens] [gi:120660324] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Identification of Small Molecule Antagonists for Thrombopoietin (TPO) Signaling Pathway | | AID | 918 | | BioAssay type | confirmatory | | Target | Thrombopoietin [Homo sapiens] [gi:120660324] | | PubMed | | | Data Table |  |
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| 38 | [SID11111541] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 [AID899, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 11111541 | | CID | 71398 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 | | AID | 899 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 39 | [SID11111541] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 [AID899, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 11111541 | | CID | 71398 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 | | AID | 899 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 40 | [SID11111540] | Active | Potency | 7.9433 | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway [AID895, Type: confirmatory] | NFKB1 protein [Homo sapiens] [gi:21620132] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway | | AID | 895 | | BioAssay type | confirmatory | | Target | NFKB1 protein [Homo sapiens] [gi:21620132] | | PubMed | | | Data Table |  |
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| 41 | [SID11111540] | Active | Potency | 7.9433 | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway [AID895, Type: confirmatory] | NFKB1 protein [Homo sapiens] [gi:21620132] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway | | AID | 895 | | BioAssay type | confirmatory | | Target | NFKB1 protein [Homo sapiens] [gi:21620132] | | PubMed | | | Data Table |  |
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| 42 | [SID11111540] | Active | Potency | 7.9433 | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway [AID895, Type: confirmatory] | NFKB1 protein [Homo sapiens] [gi:21620132] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway | | AID | 895 | | BioAssay type | confirmatory | | Target | NFKB1 protein [Homo sapiens] [gi:21620132] | | PubMed | | | Data Table |  |
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| 43 | [SID11111540] | Active | Potency | 7.9433 | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway [AID895, Type: confirmatory] | NFKB1 protein [Homo sapiens] [gi:21620132] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Identification of Small Molecule Antagonists for NFkB Signaling Pathway | | AID | 895 | | BioAssay type | confirmatory | | Target | NFKB1 protein [Homo sapiens] [gi:21620132] | | PubMed | | | Data Table |  |
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| 44 | [SID90341429] | Active | Potency | 9.4662 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 9.4662 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488773 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 45 | [SID90341429] | Active | Potency | 9.4662 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 90341429 | | CID | 71398 | | Outcome | Active | | Potency | 9.4662 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488773 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 46 | [SID50106727] | Active | Potency | 10 | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line W2 [AID1883, Type: confirmatory] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line W2 | | AID | 1883 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID50106727] | Active | Potency | 11.2202 | qHTS Validation Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2353, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2353 | | 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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| 48 | [SID50106727] | Active | Potency | 11.2202 | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
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| 49 | [SID50106727] | Active | Potency | 11.2202 | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 50106727 | | CID | 71398 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
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| 50 | [SID11111540] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 [AID883, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 11111540 | | CID | 71398 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 | | AID | 883 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
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