| 1 | [SID17414670] | Active | Potency | 2.8184 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 2.8184 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
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| 2 | [SID17414670] | Active | Potency | 2.8184 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 2.8184 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
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| 3 | [SID17414670] | Active | Potency | 3.5481 | 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 | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 3.5481 [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 |  |
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| 4 | [SID17414670] | Active | Potency | 3.5481 | 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. | 4 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 3.5481 [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 |  |
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| 5 | [SID17414670] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 6.3096 [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 |  |
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| 6 | [SID17414670] | Active | Potency | 6.3096 | 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 | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 6.3096 [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 |  |
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| 7 | [SID17414670] | Active | Potency | 10 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | | AID | 485364 | | BioAssay type | confirmatory | | Target | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | | PubMed | | | Data Table |  |
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| 8 | [SID17414670] | Active | Potency | 15.8489 | 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. | 8 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) | | AID | 881 | | BioAssay type | confirmatory | | Target | Arachidonate 15-lipoxygenase B [gi:317373425] | | PubMed | | | Data Table |  |
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| 9 | [SID17414670] | Active | Potency | 19.9526 | 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. | 9 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 19.9526 [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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| 10 | [SID17414670] | Active | Potency | 19.9526 | 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. | 10 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 19.9526 [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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| 11 | [SID17414670] | Active | Potency | 19.9526 | 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. | 11 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 19.9526 [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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| 12 | [SID17414670] | Active | Potency | 22.3872 | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2549, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 22.3872 [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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| 13 | [SID17414670] | Active | Potency | 22.3872 | 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. | 13 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 22.3872 [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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| 14 | [SID17414670] | Active | Potency | 22.3872 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 22.3872 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
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| 15 | [SID17414670] | Active | Potency | 22.3872 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 22.3872 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
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| 16 | [SID17414670] | Active | Potency | 25.1189 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
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| 17 | [SID17414670] | Active | Potency | 25.1189 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
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| 18 | [SID17414670] | Active | Potency | 28.1838 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 28.1838 [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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| 19 | [SID17414670] | Active | Potency | 28.1838 | 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. | 19 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 28.1838 [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 |  |
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| 20 | [SID17414670] | Active | Potency | 31.6228 | 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. | 20 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 31.6228 [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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| 21 | [SID17414670] | Active | Potency | 31.6228 | 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. | 21 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 31.6228 [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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| 22 | [SID17414670] | Active | Potency | 39.8107 | qHTS for Inhibitors of WRN Helicase [AID651768, Type: confirmatory] | WRN [Homo sapiens] [gi:3719421] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS for Inhibitors of WRN Helicase | | AID | 651768 | | BioAssay type | confirmatory | | Target | WRN [Homo sapiens] [gi:3719421] | | PubMed | | | Data Table |  |
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| 23 | [SID17414670] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) [AID463082, Type: screening] | PLA2G7 gene product [Homo sapiens] [gi:270133071] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | | AID | 463082 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 24 | [SID17414670] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) [AID463082, Type: screening] | PLA2G7 gene product [Homo sapiens] [gi:270133071] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | | AID | 463082 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 25 | [SID17414670] | Active | | | Fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH; PLA2G7) [AID463230, Type: screening] | PLA2G7 gene product [Homo sapiens] [gi:270133071] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH; PLA2G7) | | AID | 463230 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 26 | [SID17414670] | Active | | | Fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH; PLA2G7) [AID463230, Type: screening] | PLA2G7 gene product [Homo sapiens] [gi:270133071] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH; PLA2G7) | | AID | 463230 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 27 | [SID17414670] | Active | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
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| 28 | [SID17414670] | Active | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
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| 29 | [SID17414670] | Active | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
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| 30 | [SID17414670] | Active | | | Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 [AID1672, Type: screening] | inward rectifier potassium channel 2 [Mus musculus] [gi:6680530] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | | AID | 1672 | | BioAssay type | screening | | Target | inward rectifier potassium channel 2 [Mus musculus] [gi:6680530] | | PubMed | | | Data Table |  |
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| 31 | [SID17414670] | Active | | | Luminescence-based biochemical high throughput validation assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-1 (PLIN1) [AID493027, Type: screening] | ABHD5 gene product [Homo sapiens] [gi:31542303] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Luminescence-based biochemical high throughput validation assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-1 (PLIN1) | | AID | 493027 | | BioAssay type | screening | | Target | ABHD5 gene product [Homo sapiens] [gi:31542303] | | PubMed | | | Data Table |  |
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| 32 | [SID17414670] | Active | | | Luminescence-based biochemical high throughput validation assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) [AID493035, Type: screening] | ABHD5 gene product [Homo sapiens] [gi:31542303] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Luminescence-based biochemical high throughput validation assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) | | AID | 493035 | | BioAssay type | screening | | Target | ABHD5 gene product [Homo sapiens] [gi:31542303] | | PubMed | | | Data Table |  |
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| 33 | [SID17414670] | Active | | | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) [AID602281, Type: screening] | ABHD5 gene product [Homo sapiens] [gi:31542303] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) | | AID | 602281 | | BioAssay type | screening | | Target | ABHD5 gene product [Homo sapiens] [gi:31542303] | | PubMed | | | Data Table |  |
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| 34 | [SID17414670] | Active | | | KCNK9 specificity screen for compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 [AID2329, Type: screening] | KCNK9 gene product [Homo sapiens] [gi:7706135] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | KCNK9 specificity screen for compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | | AID | 2329 | | BioAssay type | screening | | Target | KCNK9 gene product [Homo sapiens] [gi:7706135] | | PubMed | | | Data Table |  |
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| 35 | [SID17414670] | Active | | | Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 [AID488922, Type: screening] | KCNK9 gene product [Homo sapiens] [gi:7706135] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the two-pore domain potassium channel KCNK9 | | AID | 488922 | | BioAssay type | screening | | Target | KCNK9 gene product [Homo sapiens] [gi:7706135] | | PubMed | | | Data Table |  |
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| 36 | [SID17414670] | Active | | | Second counter screen for compounds that modulate the two-pore domain potassium channel (KCNK9) [AID492997, Type: screening] | KCNK9 gene product [Homo sapiens] [gi:7706135] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Second counter screen for compounds that modulate the two-pore domain potassium channel (KCNK9) | | AID | 492997 | | BioAssay type | screening | | Target | KCNK9 gene product [Homo sapiens] [gi:7706135] | | PubMed | | | Data Table |  |
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| 37 | [SID17414670] | Active | | | Confirmatory screen for identification of compounds that inhibit the two-pore domain potassium channel (KCNK9) [AID492992, Type: screening] | KCNK9 gene product [Homo sapiens] [gi:7706135] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Confirmatory screen for identification of compounds that inhibit the two-pore domain potassium channel (KCNK9) | | AID | 492992 | | BioAssay type | screening | | Target | KCNK9 gene product [Homo sapiens] [gi:7706135] | | PubMed | | | Data Table |  |
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| 38 | [SID17414670] | Active | | | uHTS Colorimetric assay for identification of inhibitors of Scp-1 [AID493091, Type: screening] | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | uHTS Colorimetric assay for identification of inhibitors of Scp-1 | | AID | 493091 | | BioAssay type | screening | | Target | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] | | PubMed | | | Data Table |  |
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| 39 | [SID17414670] | Active | | | Confirmatory screen for compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 [AID2032, Type: screening] | inward rectifier potassium channel 2 [Mus musculus] [gi:6680530] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Confirmatory screen for compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | | AID | 2032 | | BioAssay type | screening | | Target | inward rectifier potassium channel 2 [Mus musculus] [gi:6680530] | | PubMed | | | Data Table |  |
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| 40 | [SID17414670] | Active | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. [AID1439, Type: screening] | RGS7 [Homo sapiens] [gi:1166512] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. | | AID | 1439 | | BioAssay type | screening | | Target | RGS7 [Homo sapiens] [gi:1166512] | | PubMed | | | Data Table |  |
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| 41 | [SID17414670] | Active | IC50 | | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) [AID2012, Type: confirmatory] | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | IC50 | [uM] | | BioAssay | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) | | AID | 2012 | | BioAssay type | confirmatory | | Target | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] | | PubMed | | | Data Table |  |
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| 42 | [SID17414670] | Active | | | Counterscreen for inhibitors of PP5: fluorescence-based biochemical high throughput primary assay to identify inhibitors of Protein Phosphatase 1 (PP1). [AID2235, Type: screening] | PPP1CA gene product [Homo sapiens] [gi:56790945] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of PP5: fluorescence-based biochemical high throughput primary assay to identify inhibitors of Protein Phosphatase 1 (PP1). | | AID | 2235 | | BioAssay type | screening | | Target | PPP1CA gene product [Homo sapiens] [gi:56790945] | | PubMed | | | Data Table |  |
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| 43 | [SID17414670] | Active | | | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) [AID727, Type: screening] | Focal adhesion kinase 1 [gi:3183518] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) | | AID | 727 | | BioAssay type | screening | | Target | Focal adhesion kinase 1 [gi:3183518] | | PubMed | | | Data Table |  |
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| 44 | [SID17414670] | Active | | | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) [AID727, Type: screening] | Focal adhesion kinase 1 [gi:3183518] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary biochemical high-throughput screening assay for inhibitors of Focal Adhesion Kinase (FAK) | | AID | 727 | | BioAssay type | screening | | Target | Focal adhesion kinase 1 [gi:3183518] | | PubMed | | | Data Table |  |
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| 45 | [SID17414670] | Active | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 46 | [SID17414670] | Active | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 47 | [SID17414670] | Active | | | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels [AID2156, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels | | AID | 2156 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
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| 48 | [SID17414670] | Active | | | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels [AID2156, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ2 potassium channels | | AID | 2156 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
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| 49 | [SID17414670] | Active | | | uHTS identification of inhibitors of NadD in a Colorimetric assay [AID602399, Type: screening] | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | uHTS identification of inhibitors of NadD in a Colorimetric assay | | AID | 602399 | | BioAssay type | screening | | Target | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] | | PubMed | | | Data Table |  |
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| 50 | [SID17414670] | Active | | | Screen for Chemicals that Inhibit the RAM Network [AID868, Type: screening] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 17414670 | | CID | 2928562 | | Outcome | Active | | BioAssay | Screen for Chemicals that Inhibit the RAM Network | | AID | 868 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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