| 1 | [SID50106719] | Active | Potency | 0.1995 | Confirmation Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID489007, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.1995 [uM] | | BioAssay | Confirmation Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 489007 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|
| 2 | [SID50106719] | Active | Potency | 0.3981 | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.3981 [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|
| 3 | [SID50106719] | Active | Potency | 0.4467 | 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. | 3 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.4467 [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 |  |
|
| 4 | [SID50106719] | Active | Potency | 0.5012 | qHTS Validation Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID1705, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.5012 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 1705 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
|
| 5 | [SID90341525] | Active | Potency | 0.5012 | 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. | 5 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 0.5012 [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 |  |
|
| 6 | [SID50106719] | Active | Potency | 0.631 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.631 [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 |  |
|
| 7 | [SID50106719] | Active | Potency | 0.631 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.631 [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 |  |
|
| 8 | [SID50106719] | Active | Potency | 0.7079 | Confirmation qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2572, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.7079 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2572 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
|
| 9 | [SID50106719] | Active | Potency | 0.7943 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.7943 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
|
| 10 | [SID50106719] | Active | Potency | 0.7943 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.7943 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
|
| 11 | [SID50106719] | Active | Potency | 0.8913 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.8913 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 12 | [SID50106719] | Active | Potency | 0.8913 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 0.8913 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 13 | [SID90341525] | Active | Potency | 0.9466 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 0.9466 [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 |  |
|
| 14 | [SID90341525] | Active | Potency | 0.9466 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 0.9466 [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 |  |
|
| 15 | [SID90341525] | Active | Potency | 0.9466 | 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. | 15 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 0.9466 [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 |  |
|
| 16 | [SID90341525] | Active | Potency | 0.9466 | 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. | 16 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 0.9466 [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 |  |
|
| 17 | [SID50106719] | Active | Potency | 1.122 | 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. | 17 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 1.122 [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 |  |
|
| 18 | [SID50106719] | Active | Potency | 1.2589 | 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. | 18 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 1.2589 [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 |  |
|
| 19 | [SID50106719] | Active | Potency | 1.2589 | 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. | 19 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 1.2589 [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 |  |
|
| 20 | [SID11111500] | Active | Potency | 1.5849 | 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. | 20 | | Structure |
| | Substance | | | SID | 11111500 | | CID | 5353329 | | Outcome | Active | | Potency | 1.5849 [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 |  |
|
| 21 | [SID90341525] | Active | Potency | 1.5849 | qHTS Validation Assay for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails [AID488953, Type: confirmatory] | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails | | AID | 488953 | | BioAssay type | confirmatory | | Target | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] | | PubMed | | | Data Table |  |
|
| 22 | [SID90341525] | Active | Potency | 2.3778 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 2.3778 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 23 | [SID90341525] | Active | Potency | 2.3778 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 2.3778 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 24 | [SID90341525] | Active | Potency | 2.3778 | qHTS Validation Assay for Inhibitors for MPP8 Chromodomain Interactions with Methylated Histone Tails [AID488949, Type: confirmatory] | MPHOSPH8 gene product [Homo sapiens] [gi:41055989] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 2.3778 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors for MPP8 Chromodomain Interactions with Methylated Histone Tails | | AID | 488949 | | BioAssay type | confirmatory | | Target | MPHOSPH8 gene product [Homo sapiens] [gi:41055989] | | PubMed | | | Data Table |  |
|
| 25 | [SID85231143] | Active | Potency | 2.5119 | qHTS Validation Assay for Inhibitors for MPP8 Chromodomain Interactions with Methylated Histone Tails [AID488949, Type: confirmatory] | MPHOSPH8 gene product [Homo sapiens] [gi:41055989] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 85231143 | | CID | 5353329 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors for MPP8 Chromodomain Interactions with Methylated Histone Tails | | AID | 488949 | | BioAssay type | confirmatory | | Target | MPHOSPH8 gene product [Homo sapiens] [gi:41055989] | | PubMed | | | Data Table |  |
|
| 26 | [SID50106719] | Active | Potency | 2.5119 | 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. | 26 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 27 | [SID50106719] | Active | Potency | 2.5119 | 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. | 27 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 28 | [SID90341525] | Active | Potency | 2.6679 | 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. | 28 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 2.6679 [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 |  |
|
| 29 | [SID90341525] | Active | Potency | 2.6679 | 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. | 29 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 2.6679 [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 |  |
|
| 30 | [SID50106719] | Active | Potency | 3.5481 | 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. | 30 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 3.5481 [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 |  |
|
| 31 | [SID17405840] | Active | IC50 | 3.92172 | Dose Response Confirmation for DnaK Inhibitors [AID1462, Type: confirmatory] | heat shock protein [Escherichia coli str. K-12 substr. MG1655] [gi:16130533] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 17405840 | | CID | 5353329 | | Outcome | Active | | IC50 | 3.92172 [uM] | | BioAssay | Dose Response Confirmation for DnaK Inhibitors | | AID | 1462 | | BioAssay type | confirmatory | | Target | heat shock protein [Escherichia coli str. K-12 substr. MG1655] [gi:16130533] | | PubMed | | | Data Table |  |
|
| 32 | [SID11111500] | 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. | 32 | | Structure |
| | Substance | | | SID | 11111500 | | CID | 5353329 | | 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 |  |
|
| 33 | [SID90341525] | Active | Potency | 4.14 | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter [AID463106, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 4.14 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter | | AID | 463106 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 34 | [SID90341525] | Active | Potency | 4.14 | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter [AID463106, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 4.14 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter | | AID | 463106 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 35 | [SID90341525] | Active | Potency | 4.4668 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 4.4668 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 36 | [SID90341525] | Active | Potency | 4.4668 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 4.4668 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 37 | [SID90341525] | Active | Potency | 4.7755 | qHTS Validation Assay to Find Inhibitors of Pin1 [AID504536, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 4.7755 [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of Pin1 | | AID | 504536 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
|
| 38 | [SID90341525] | Active | Potency | 4.7755 | qHTS Validation Assay to Find Inhibitors of Pin1 [AID504536, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 4.7755 [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of Pin1 | | AID | 504536 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
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| 39 | [SID50106719] | Active | Potency | 5.0119 | qHTS Assay for Inhibitors of Influenza NS1 Protein Function [AID2326, Type: confirmatory] | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Inhibitors of Influenza NS1 Protein Function | | AID | 2326 | | BioAssay type | confirmatory | | Target | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] | | PubMed | | | Data Table |  |
|
| 40 | [SID50106719] | 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. | 40 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | 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 |  |
|
| 41 | [SID90341525] | Active | Potency | 5.9728 | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS [AID504845, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 5.9728 [uM] | | BioAssay | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS | | AID | 504845 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] | | PubMed | | | Data Table |  |
|
| 42 | [SID90341525] | Active | Potency | 5.9728 | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS [AID504845, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 5.9728 [uM] | | BioAssay | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS | | AID | 504845 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] | | PubMed | | | Data Table |  |
|
| 43 | [SID90341525] | Active | Potency | 5.9728 | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS [AID504845, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 5.9728 [uM] | | BioAssay | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS | | AID | 504845 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] | | PubMed | | | Data Table |  |
|
| 44 | [SID90341525] | Active | Potency | 6.012 | qHTS Validation Assay to Find Inhibitors of Phosphoglycerate Kinase [AID504547, Type: confirmatory] | phosphoglycerate kinase [Trypanosoma brucei] [gi:115503961] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 90341525 | | CID | 5353329 | | Outcome | Active | | Potency | 6.012 [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of Phosphoglycerate Kinase | | AID | 504547 | | BioAssay type | confirmatory | | Target | phosphoglycerate kinase [Trypanosoma brucei] [gi:115503961] | | PubMed | | | Data Table |  |
|
| 45 | [SID50106719] | Active | Potency | 6.3096 | qHTS Validation Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2364, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Bloom's syndrome helicase (BLM) | | AID | 2364 | | BioAssay type | confirmatory | | Target | Bloom syndrome protein [Homo sapiens] [gi:4557365] | | PubMed | | | Data Table |  |
|
| 46 | [SID50106719] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 6.3096 [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 |  |
|
| 47 | [SID11111500] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) [AID892, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 11111500 | | CID | 5353329 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) | | AID | 892 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 48 | [SID50106719] | Active | Potency | 7.9433 | qHTS for inhibitors of binding or entry into cells for Marburg Virus [AID540276, Type: confirmatory] | gene 4 small orf - Marburg virus [gi:420597] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS for inhibitors of binding or entry into cells for Marburg Virus | | AID | 540276 | | BioAssay type | confirmatory | | Target | gene 4 small orf - Marburg virus [gi:420597] | | PubMed | | | Data Table |  |
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| 49 | [SID50106719] | Active | Potency | 8.9125 | Counterscreen for APE1 Inhibitors: qHTS Validation Assay for Inhibitors of Endonuclease IV [AID1708, Type: confirmatory] | endonuclease IV [Escherichia coli] [gi:405898] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | Counterscreen for APE1 Inhibitors: qHTS Validation Assay for Inhibitors of Endonuclease IV | | AID | 1708 | | BioAssay type | confirmatory | | Target | endonuclease IV [Escherichia coli] [gi:405898] | | PubMed | | | Data Table |  |
|
| 50 | [SID50106719] | Active | Potency | 8.9125 | 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 | 50106719 | | CID | 5353329 | | Outcome | Active | | Potency | 8.9125 [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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