| 1 | [SID99343744] | Chemical Probe | | | Probe Development Summary for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2407, Type: summary] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 99343744 | | CID | 3245059 | | Outcome | Chemical Probe | | BioAssay | Probe Development Summary for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2407 | | BioAssay type | summary | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 2 | [SID99343744] | Chemical Probe | | | Probe Development Summary for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2407, Type: summary] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 99343744 | | CID | 3245059 | | Outcome | Chemical Probe | | BioAssay | Probe Development Summary for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2407 | | BioAssay type | summary | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 3 | [SID99343744] | Chemical Probe | | | Probe Development Summary for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2407, Type: summary] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 99343744 | | CID | 3245059 | | Outcome | Chemical Probe | | BioAssay | Probe Development Summary for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2407 | | BioAssay type | summary | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 4 | [SID4251360] | Active | Potency | 0.1413 | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2429, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | Potency | 0.1413 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2429 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 5 | [SID4251360] | Active | Potency | 0.1413 | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2429, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | Potency | 0.1413 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2429 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 6 | [SID4251360] | Active | Potency | 0.1413 | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2429, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | Potency | 0.1413 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2429 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 7 | [SID87550717] | Active | Potency | 0.1413 | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2429, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Active | | Potency | 0.1413 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2429 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 8 | [SID87550717] | Active | Potency | 0.1413 | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2429, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Active | | Potency | 0.1413 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2429 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 9 | [SID87550717] | Active | Potency | 0.1413 | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2429, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Active | | Potency | 0.1413 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2429 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 10 | [SID4251360] | Active | Potency | 0.2239 | 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 | 4251360 | | CID | 3245059 | | Outcome | Active | | Potency | 0.2239 [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 | [SID4251360] | Active | Potency | 0.2239 | 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 | 4251360 | | CID | 3245059 | | Outcome | Active | | Potency | 0.2239 [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 | [SID4251360] | Active | Potency | 0.2239 | 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. | 12 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | Potency | 0.2239 [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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| 13 | [SID4251360] | Active | | | Parallel artificial membrane permeability assay at pH 7.4 [AID624339, Type: other] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | BioAssay | Parallel artificial membrane permeability assay at pH 7.4 | | AID | 624339 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 14 | [SID87550717] | Active | | | Thermal Shift Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2427, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Active | | BioAssay | Thermal Shift Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2427 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 15 | [SID87550717] | Active | | | Thermal Shift Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2427, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Active | | BioAssay | Thermal Shift Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2427 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 16 | [SID87550717] | Active | | | Thermal Shift Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID2427, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Active | | BioAssay | Thermal Shift Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 2427 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 17 | [SID4251360] | Active | | | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) [AID624268, Type: screening] | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | BioAssay | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | | AID | 624268 | | BioAssay type | screening | | Target | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] | | PubMed | | | Data Table |  |
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| 18 | [SID4251360] | Active | | | Luminescence-based biochemical high throughput confirmation assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) [AID624412, Type: screening] | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | BioAssay | Luminescence-based biochemical high throughput confirmation assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | | AID | 624412 | | BioAssay type | screening | | Target | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] | | PubMed | | | Data Table |  |
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| 19 | [SID4251360] | Active | | | Fluorescent Polarization-based biochemical high throughput orthogonal assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) [AID651607, Type: screening] | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Active | | BioAssay | Fluorescent Polarization-based biochemical high throughput orthogonal assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | | AID | 651607 | | BioAssay type | screening | | Target | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] | | PubMed | | | Data Table |  |
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| 20 | [SID4251360] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 21 | [SID4251360] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 22 | [SID4251360] | Unspecified | | | Plasma Stability Mouse - Set 2 [AID624419, Type: other] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Unspecified | | BioAssay | Plasma Stability Mouse - Set 2 | | AID | 624419 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 23 | [SID4251360] | Unspecified | | | Plasma Stability Human - 2 [AID624420, Type: other] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Unspecified | | BioAssay | Plasma Stability Human - 2 | | AID | 624420 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 24 | [SID4251360] | Unspecified | | | Early assessment of compound stability in 1x PBS - Set 2 [AID624456, Type: other] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Unspecified | | BioAssay | Early assessment of compound stability in 1x PBS - Set 2 | | AID | 624456 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 25 | [SID4251360] | Unspecified | | | Human hepatic microsome stability-Set 2 [AID624452, Type: screening] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Unspecified | | BioAssay | Human hepatic microsome stability-Set 2 | | AID | 624452 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 26 | [SID4251360] | Unspecified | | | Mouse hepatic microsome stability - Set 2 [AID624451, Type: screening] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Unspecified | | BioAssay | Mouse hepatic microsome stability - Set 2 | | AID | 624451 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 27 | [SID4251360] | Inactive | Potency | 22.3872 | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide [AID1768, Type: confirmatory] | MEN1 gene product [Homo sapiens] [gi:18860839] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | Potency | 22.3872 [uM] | | BioAssay | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide | | AID | 1768 | | BioAssay type | confirmatory | | Target | MEN1 gene product [Homo sapiens] [gi:18860839] | | PubMed | | | Data Table |  |
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| 28 | [SID87550717] | Inactive | Potency | 39.8107 | qHTS Assay to Find Inhibitors of Pin1 [AID504891, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Pin1 | | AID | 504891 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
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| 29 | [SID87550717] | Inactive | Potency | 39.8107 | qHTS Assay to Find Inhibitors of Pin1 [AID504891, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Pin1 | | AID | 504891 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
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| 30 | [SID4251360] | Inactive | Potency | 100 | 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. | 30 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | Potency | 100 [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 |  |
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| 31 | [SID4251360] | Inactive | IC50 | 100 | Chemical Antagonists IAP-family anti-apoptotic proteins [AID1018, Type: confirmatory] | X-linked inhibitor of apoptosis [Homo sapiens] [gi:8744934] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | IC50 | 100 [uM] | | BioAssay | Chemical Antagonists IAP-family anti-apoptotic proteins | | AID | 1018 | | BioAssay type | confirmatory | | Target | X-linked inhibitor of apoptosis [Homo sapiens] [gi:8744934] | | PubMed | | | Data Table |  |
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| 32 | [SID4251360] | Inactive | IC50 | 100 | Counter Screen using XIAP-Bir3 for Chemical Antagonists of Bir1/2 domains of IAP-family anti-apoptotic proteins [AID1513, Type: confirmatory] | X-linked inhibitor of apoptosis [Homo sapiens] [gi:8744934] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | IC50 | 100 [uM] | | BioAssay | Counter Screen using XIAP-Bir3 for Chemical Antagonists of Bir1/2 domains of IAP-family anti-apoptotic proteins | | AID | 1513 | | BioAssay type | confirmatory | | Target | X-linked inhibitor of apoptosis [Homo sapiens] [gi:8744934] | | PubMed | | | Data Table |  |
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| 33 | [SID4251360] | Inactive | | | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Primary Screen [AID1066, Type: screening] | acetyl-CoA acetyltransferase/HMG-CoA reductase [Enterococcus faecalis] [gi:9937384] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Primary Screen | | AID | 1066 | | BioAssay type | screening | | Target | acetyl-CoA acetyltransferase/HMG-CoA reductase [Enterococcus faecalis] [gi:9937384] | | PubMed | | | Data Table |  |
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| 34 | [SID4251360] | Inactive | Potency | | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
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| 35 | [SID4251360] | Inactive | | | uHTS identification of small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay [AID504690, Type: screening] | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay | | AID | 504690 | | BioAssay type | screening | | Target | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] | | PubMed | | | Data Table |  |
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| 36 | [SID4251360] | Inactive | Potency | | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | Potency | [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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| 37 | [SID87550717] | Inactive | Potency | | 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. | 37 | | Structure |
| | Substance | | | SID | 87550717 | | CID | 3245059 | | Outcome | Inactive | | Potency | [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 |  |
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| 38 | [SID4251360] | Inactive | Potency | | 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. | 38 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | Potency | [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 |  |
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| 39 | [SID4251360] | Inactive | | | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase [AID1556, Type: screening] | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase | | AID | 1556 | | BioAssay type | screening | | Target | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] | | PubMed | | | Data Table |  |
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| 40 | [SID4251360] | Inactive | | | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin [AID2314, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin | | AID | 2314 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
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| 41 | [SID4251360] | Inactive | | | A qHTS for Small Molecule Inhibitors of Shiga Toxin [AID2315, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | A qHTS for Small Molecule Inhibitors of Shiga Toxin | | AID | 2315 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
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| 42 | [SID4251360] | Inactive | IC50 | | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. [AID1986, Type: confirmatory] | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. | | AID | 1986 | | BioAssay type | confirmatory | | Target | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | | PubMed | | | Data Table |  |
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| 43 | [SID4251360] | Inactive | | | Primary cell-based high-throughput screening assay for inhibitors of TLR4-MyD88 binding [AID861, Type: screening] | toll-like receptor 4 [Homo sapiens] [gi:55662034] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for inhibitors of TLR4-MyD88 binding | | AID | 861 | | BioAssay type | screening | | Target | toll-like receptor 4 [Homo sapiens] [gi:55662034] | | PubMed | | | Data Table |  |
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| 44 | [SID4251360] | Inactive | | | QFRET-based counterscreen for PFM18AAP inhibitors: biochemical high throughput screening assay to identify inhibitors of the Cathepsin L proteinase (CTSL1). [AID1906, Type: screening] | cathepsin L1 [Homo sapiens] [gi:55958172] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | QFRET-based counterscreen for PFM18AAP inhibitors: biochemical high throughput screening assay to identify inhibitors of the Cathepsin L proteinase (CTSL1). | | AID | 1906 | | BioAssay type | screening | | Target | cathepsin L1 [Homo sapiens] [gi:55958172] | | PubMed | | | Data Table |  |
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| 45 | [SID4251360] | Inactive | | | Counterscreen for procaspase-3 activators: absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-7 [AID463210, Type: screening] | caspase 7, apoptosis-related cysteine peptidase [Homo sapiens] [gi:55960760] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | Counterscreen for procaspase-3 activators: absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-7 | | AID | 463210 | | BioAssay type | screening | | Target | caspase 7, apoptosis-related cysteine peptidase [Homo sapiens] [gi:55960760] | | PubMed | | | Data Table |  |
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| 46 | [SID4251360] | Inactive | | | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype [AID761, Type: screening] | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype | | AID | 761 | | BioAssay type | screening | | Target | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] | | PubMed | | | Data Table |  |
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| 47 | [SID4251360] | Inactive | | | Primary HTS assay for chemical inhibitors of TNF alpha stimulated E-Selectin expression [AID1246, Type: screening] | selectin E (endothelial adhesion molecule 1) [Homo sapiens] [gi:56417702] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | Primary HTS assay for chemical inhibitors of TNF alpha stimulated E-Selectin expression | | AID | 1246 | | BioAssay type | screening | | Target | selectin E (endothelial adhesion molecule 1) [Homo sapiens] [gi:56417702] | | PubMed | | | Data Table |  |
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| 48 | [SID4251360] | Inactive | Potency | | qHTS of Trypanosoma Brucei Inhibitors [AID624173, Type: confirmatory] | hypothetical protein, conserved [Trypanosoma brucei] [gi:62359610] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of Trypanosoma Brucei Inhibitors | | AID | 624173 | | BioAssay type | confirmatory | | Target | hypothetical protein, conserved [Trypanosoma brucei] [gi:62359610] | | PubMed | | | Data Table |  |
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| 49 | [SID4251360] | Inactive | | | Plate Read Microorganism-Based Primary HTS to Identify Modulators of the AI-2 Quorum Sensing System [AID2094, Type: screening] | Chain A, Crystal Structure Of The Apo Form Of Vibrio Harveyi Luxp Complexed With The Periplasmic Dom [gi:67463988] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | Plate Read Microorganism-Based Primary HTS to Identify Modulators of the AI-2 Quorum Sensing System | | AID | 2094 | | BioAssay type | screening | | Target | Chain A, Crystal Structure Of The Apo Form Of Vibrio Harveyi Luxp Complexed With The Periplasmic Dom [gi:67463988] | | PubMed | | | Data Table |  |
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| 50 | [SID4251360] | Inactive | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) [AID1706, Type: screening] | 3C-like protease [Infectious bronchitis virus] [gi:73745819] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 4251360 | | CID | 3245059 | | Outcome | Inactive | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) | | AID | 1706 | | BioAssay type | screening | | Target | 3C-like protease [Infectious bronchitis virus] [gi:73745819] | | PubMed | | | Data Table |  |
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