| 1 | [SID17409262] | Active | Potency | 0.2668 | qHTS for Inhibitors of WRN Helicase [AID651768, Type: confirmatory] | WRN [Homo sapiens] [gi:3719421] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 0.2668 [uM] | | BioAssay | qHTS for Inhibitors of WRN Helicase | | AID | 651768 | | BioAssay type | confirmatory | | Target | WRN [Homo sapiens] [gi:3719421] | | PubMed | | | Data Table |  |
|
| 2 | [SID17409262] | Active | Potency | 0.2818 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 0.2818 [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 |  |
|
| 3 | [SID17409262] | Active | Potency | 0.2818 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 0.2818 [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 |  |
|
| 4 | [SID17409262] | Active | Potency | 0.2906 | qHTS for inhibitors of Phosphogylcerate Kinase: Hit Validation Screen [AID686980, Type: confirmatory] | |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 0.2906 [uM] | | BioAssay | qHTS for inhibitors of Phosphogylcerate Kinase: Hit Validation Screen | | AID | 686980 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 5 | [SID17409262] | Active | Potency | 0.7079 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 0.7079 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 6 | [SID17409262] | Active | Potency | 0.7079 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 0.7079 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 7 | [SID17409262] | Active | Potency | 1 | 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. | 7 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 1 [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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| 8 | [SID17409262] | Active | IC50 | 1.0702 | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters [AID748, Type: confirmatory] | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 1.0702 [uM] | | BioAssay | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters | | AID | 748 | | BioAssay type | confirmatory | | Target | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] | | PubMed | | | Data Table |  |
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| 9 | [SID17409262] | Active | IC50 | 1.0702 | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters [AID748, Type: confirmatory] | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 1.0702 [uM] | | BioAssay | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters | | AID | 748 | | BioAssay type | confirmatory | | Target | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] | | PubMed | | | Data Table |  |
|
| 10 | [SID17409262] | Active | IC50 | 1.0702 | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters [AID748, Type: confirmatory] | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 1.0702 [uM] | | BioAssay | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters | | AID | 748 | | BioAssay type | confirmatory | | Target | nuclear receptor subfamily 4 group A member 1 [Homo sapiens] [gi:27894344] | | PubMed | | | Data Table |  |
|
| 11 | [SID17409262] | Active | IC50 | 1.501 | QFRET-based biochemical high throughput dose response assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID2195, Type: confirmatory] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 1.501 [uM] | | BioAssay | QFRET-based biochemical high throughput dose response assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 2195 | | BioAssay type | confirmatory | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
|
| 12 | [SID17409262] | Active | IC50 | 1.501 | QFRET-based biochemical high throughput dose response assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID2195, Type: confirmatory] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 1.501 [uM] | | BioAssay | QFRET-based biochemical high throughput dose response assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 2195 | | BioAssay type | confirmatory | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
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| 13 | [SID17409262] | Active | Potency | 1.5849 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 14 | [SID17409262] | Active | Potency | 1.5849 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 15 | [SID17409262] | Active | Potency | 1.5849 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
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| 16 | [SID17409262] | Active | Potency | 1.5849 | 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. | 16 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 1.5849 [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 |  |
|
| 17 | [SID17409262] | Active | Potency | 1.9953 | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 1.9953 [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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| 18 | [SID17409262] | Active | Potency | 1.9953 | 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. | 18 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 1.9953 [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 |  |
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| 19 | [SID17409262] | Active | Potency | 2.2387 | 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. | 19 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 2.2387 [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 |  |
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| 20 | [SID17409262] | Active | Potency | 2.2387 | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain [AID504339, Type: confirmatory] | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain | | AID | 504339 | | BioAssay type | confirmatory | | Target | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] | | PubMed | | | Data Table |  |
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| 21 | [SID17409262] | Active | Potency | 2.2387 | qHTS Assay to Find Inhibitors of Phosphoglycerate Kinase [AID602233, Type: confirmatory] | phosphoglycerate kinase [Trypanosoma brucei] [gi:115503961] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Phosphoglycerate Kinase | | AID | 602233 | | BioAssay type | confirmatory | | Target | phosphoglycerate kinase [Trypanosoma brucei] [gi:115503961] | | PubMed | | | Data Table |  |
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| 22 | [SID17409262] | Active | EC50 | 2.28 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. [AID1871, Type: confirmatory] | RGS7 [Homo sapiens] [gi:1166512] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | EC50 | 2.28 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. | | AID | 1871 | | BioAssay type | confirmatory | | Target | RGS7 [Homo sapiens] [gi:1166512] | | PubMed | | | Data Table |  |
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| 23 | [SID17409262] | Active | Potency | 2.8184 | 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. | 23 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 2.8184 [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 |  |
|
| 24 | [SID17409262] | Active | Potency | 3.1381 | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen [AID2100, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 3.1381 [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | | AID | 2100 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
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| 25 | [SID17409262] | Active | Potency | 3.1381 | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen [AID2100, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 3.1381 [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | | AID | 2100 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
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| 26 | [SID17409262] | Active | Potency | 3.1381 | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen [AID2100, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 3.1381 [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase Cleavage of Glycogen | | AID | 2100 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 27 | [SID17409262] | Active | EC50 | 3.8 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1872, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | EC50 | 3.8 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1872 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] | | PubMed | | | Data Table |  |
|
| 28 | [SID17409262] | Active | EC50 | 3.8 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1872, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | EC50 | 3.8 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1872 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] | | PubMed | | | Data Table |  |
|
| 29 | [SID17409262] | Active | EC50 | 3.8 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. [AID1872, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | EC50 | 3.8 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | | AID | 1872 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301151] | | PubMed | | | Data Table |  |
|
| 30 | [SID17409262] | Active | EC50 | 3.99 | Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1888, Type: confirmatory] | regulator of G-protein signaling 16 [Homo sapiens] [gi:156416009] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | EC50 | 3.99 [uM] | | BioAssay | Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1888 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 16 [Homo sapiens] [gi:156416009] | | PubMed | | | Data Table |  |
|
| 31 | [SID17409262] | Active | EC50 | 4.25 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. [AID1884, Type: confirmatory] | regulator of G-protein signaling 19 [Homo sapiens] [gi:86990435] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | EC50 | 4.25 [uM] | | BioAssay | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. | | AID | 1884 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 19 [Homo sapiens] [gi:86990435] | | PubMed | | | Data Table |  |
|
| 32 | [SID92117384] | Active | IC50 | 6 | Late stage assay provider results from the probe development effort to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (M18AAP): radiolabel-based cell-based dose response assay to identify compounds that inhibit P. falciparum growth in RBCs [AID489011, Type: confirmatory] | |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 92117384 | | CID | 11958779 | | Outcome | Active | | IC50 | 6 [uM] | | BioAssay | Late stage assay provider results from the probe development effort to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (M18AAP): radiolabel-based cell-based dose response assay to identify compounds that inhibit P. falciparum growth in RBCs | | AID | 489011 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 33 | [SID17409262] | Active | Potency | 6.3096 | Counterscreen for APE1 Inhibitors: Fluorescent Dye Displacement Assay [AID2564, Type: confirmatory] | |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | Counterscreen for APE1 Inhibitors: Fluorescent Dye Displacement Assay | | AID | 2564 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 34 | [SID17409262] | Active | Potency | 6.3096 | Counterscreen for APE1 Inhibitors: Confirmatory Fluorescent Dye Displacement Assay [AID2741, Type: confirmatory] | |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | Counterscreen for APE1 Inhibitors: Confirmatory Fluorescent Dye Displacement Assay | | AID | 2741 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 35 | [SID17409262] | Active | Potency | 6.7456 | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) [AID588342, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 6.7456 [uM] | | BioAssay | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) | | AID | 588342 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
|
| 36 | [SID17409262] | Active | Potency | 7.9433 | HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails [AID540317, Type: confirmatory] | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails | | AID | 540317 | | BioAssay type | confirmatory | | Target | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] | | PubMed | | | Data Table |  |
|
| 37 | [SID17409262] | Active | Potency | 12.5893 | 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. | 37 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 12.5893 [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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| 38 | [SID17409262] | 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. | 38 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | 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 |  |
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| 39 | [SID17409262] | 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. | 39 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | 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 |  |
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| 40 | [SID17409262] | Active | IC50 | 12.8 | Dose Response confirmation of uHTS hits from a small molecule inhibitors of mouse intestinal alkaline phosphatase via a luminescent assay [AID488785, Type: confirmatory] | intestinal alkaline phosphatase precursor [Mus musculus] [gi:124487323] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 12.8 [uM] | | BioAssay | Dose Response confirmation of uHTS hits from a small molecule inhibitors of mouse intestinal alkaline phosphatase via a luminescent assay | | AID | 488785 | | BioAssay type | confirmatory | | Target | intestinal alkaline phosphatase precursor [Mus musculus] [gi:124487323] | | PubMed | | | Data Table |  |
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| 41 | [SID17409262] | Active | Potency | 16.3601 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 16.3601 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 42 | [SID17409262] | Active | IC50 | 21.11 | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Primary and Confirmatory Screens [AID624330, Type: confirmatory] | RACGAP1 gene product [Homo sapiens] [gi:21361397] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 21.11 [uM] | | BioAssay | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Primary and Confirmatory Screens | | AID | 624330 | | BioAssay type | confirmatory | | Target | RACGAP1 gene product [Homo sapiens] [gi:21361397] | | PubMed | | | Data Table |  |
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| 43 | [SID17409262] | Active | IC50 | 28.77 | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Counter Screen Coupled Enzyme [AID624351, Type: confirmatory] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | IC50 | 28.77 [uM] | | BioAssay | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Counter Screen Coupled Enzyme | | AID | 624351 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 44 | [SID17409262] | Active | Potency | 39.8107 | qHTS Inhibitors of AmpC Beta-Lactamase (assay without detergent) [AID485341, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Inhibitors of AmpC Beta-Lactamase (assay without detergent) | | AID | 485341 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
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| 45 | [SID17409262] | Active | CC50 | 100 | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - HeLa Cytotoxicity [AID624300, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | CC50 | 100 [uM] | | BioAssay | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - HeLa Cytotoxicity | | AID | 624300 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 46 | [SID17409262] | Active | | | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Absorbance-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) full deck assay to identify assay artifacts [AID588335, Type: screening] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Absorbance-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) full deck assay to identify assay artifacts | | AID | 588335 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID92117384] | Active | | | Late stage assay provider results from the probe development effort to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (M18AAP): radiolabel-based cell-based assay to identify compounds that inhibit P. falciparum growth in RBCs [AID489015, Type: other] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 92117384 | | CID | 11958779 | | Outcome | Active | | BioAssay | Late stage assay provider results from the probe development effort to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (M18AAP): radiolabel-based cell-based assay to identify compounds that inhibit P. falciparum growth in RBCs | | AID | 489015 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 48 | [SID17409262] | Active | Potency | | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) [AID652105, Type: confirmatory] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) | | AID | 652105 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID17409262] | Active | | | uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay [AID686954, Type: screening] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of Artemis endonuclease activity via a fluorescence intensity assay | | AID | 686954 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID17409262] | Active | | | Counterscreen for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl): Fluorescence-based biochemical high throughput assay to identify GFP inhibitors and fluorescence quenchers [AID602125, Type: screening] | green fluorescent protein [Aequorea victoria] [gi:634009] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 17409262 | | CID | 11958779 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl): Fluorescence-based biochemical high throughput assay to identify GFP inhibitors and fluorescence quenchers | | AID | 602125 | | BioAssay type | screening | | Target | green fluorescent protein [Aequorea victoria] [gi:634009] | | PubMed | | | Data Table |  |
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