| 1 | [SID8150002] | Active | | | Suppression of Polyglutamine Toxicity in Whole Organism Drosophila Model of SCA1 (SCA1FLYe) [AID1595, Type: other] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Active | | BioAssay | Suppression of Polyglutamine Toxicity in Whole Organism Drosophila Model of SCA1 (SCA1FLYe) | | AID | 1595 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID8150002] | Active | | | Suppression of Polyglutamine Toxicity in Whole Organism Drosophila Model of SCA1 (SCA1FLYp) [AID1597, Type: other] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Active | | BioAssay | Suppression of Polyglutamine Toxicity in Whole Organism Drosophila Model of SCA1 (SCA1FLYp) | | AID | 1597 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 3 | [SID57260141] | 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. | 3 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | 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 |  |
|
| 4 | [SID57260141] | 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. | 4 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | 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 |  |
|
| 5 | [SID57260141] | Active | | | Phenotypic HTS multiplex for antifungal efflux pump inhibitors [AID485275, Type: screening] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Active | | BioAssay | Phenotypic HTS multiplex for antifungal efflux pump inhibitors | | AID | 485275 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 6 | [SID57260141] | Active | | | uHTS Fluorescent Assay Using Nedd8 Protein Substrate for Identification of Inhibitors of Sentrin-Specific Protease 8 (SENP8) [AID602440, Type: screening] | SENP8 gene product [Homo sapiens] [gi:262118306] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Active | | BioAssay | uHTS Fluorescent Assay Using Nedd8 Protein Substrate for Identification of Inhibitors of Sentrin-Specific Protease 8 (SENP8) | | AID | 602440 | | BioAssay type | screening | | Target | SENP8 gene product [Homo sapiens] [gi:262118306] | | PubMed | | | Data Table |  |
|
| 7 | [SID57260141] | Active | | | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID463190, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 463190 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
|
| 8 | [SID103641027] | Unspecified | | | Literature-mined public compounds from Greene et al multi-species hepatotoxicity modelling dataset [AID588209, Type: Literature] | |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103641027 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Literature-mined public compounds from Greene et al multi-species hepatotoxicity modelling dataset | | AID | 588209 | | BioAssay type | Literature | | Target | | | PubMed | 20553011 | | Data Table |  |
|
| 9 | [SID103641027] | Unspecified | | | Human drug-induced liver injury (DILI) modelling dataset from Ekins et al [AID588210, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103641027 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Human drug-induced liver injury (DILI) modelling dataset from Ekins et al | | AID | 588210 | | BioAssay type | Literature | | Target | | | PubMed | 20843939 | | Data Table |  |
|
| 10 | [SID57260141] | 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. | 10 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | 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 |  |
|
| 11 | [SID57260141] | 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. | 11 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | 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 |  |
|
| 12 | [SID103641027] | Unspecified | | | Induction of CRABP 2 mRNA expression in human normal fibroblast at 1 uM by western blot relative to control [AID404775, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103641027 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Induction of CRABP 2 mRNA expression in human normal fibroblast at 1 uM by western blot relative to control | | AID | 404775 | | BioAssay type | Literature | | Target | | | PubMed | 18511283 | | Data Table |  |
|
| 13 | [SID103641027] | Unspecified | | | Induction of CRABP 2 mRNA expression in human normal fibroblast at 10 uM by western blot relative to control [AID404776, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103641027 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Induction of CRABP 2 mRNA expression in human normal fibroblast at 10 uM by western blot relative to control | | AID | 404776 | | BioAssay type | Literature | | Target | | | PubMed | 18511283 | | Data Table |  |
|
| 14 | [SID8150002] | Unspecified | | | Screen for compounds that induce the human heat shock transcriptional response (HSEluc) [AID1611, Type: other] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screen for compounds that induce the human heat shock transcriptional response (HSEluc) | | AID | 1611 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 15 | [SID8150002] | Unspecified | | | Screen for compounds that increase glutamate transport activity in MN-1 cell line (GluUPTAKE) [AID1612, Type: other] | |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screen for compounds that increase glutamate transport activity in MN-1 cell line (GluUPTAKE) | | AID | 1612 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 16 | [SID8150002] | Unspecified | | | Screen for compounds that inhibit protein aggregation formed by mutant SOD1 (GFPSOD1) [AID1613, Type: other] | |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screen for compounds that inhibit protein aggregation formed by mutant SOD1 (GFPSOD1) | | AID | 1613 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 17 | [SID8150002] | Unspecified | | | Screen for compounds that reduce polyglutamine (polyQ) inclusions in nerve growth factor (NGF)-treated PC12 cells (GFPQ80) [AID1614, Type: other] | |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screen for compounds that reduce polyglutamine (polyQ) inclusions in nerve growth factor (NGF)-treated PC12 cells (GFPQ80) | | AID | 1614 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 18 | [SID8150002] | Unspecified | | | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubH) [AID1616, Type: other] | |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubH) | | AID | 1616 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 19 | [SID8150002] | Unspecified | | | Screen for compounds that selectively inhibit cytochrome c release from purified mitochondria (CytoCRel) [AID1603, Type: other] | |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screen for compounds that selectively inhibit cytochrome c release from purified mitochondria (CytoCRel) | | AID | 1603 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 20 | [SID8150002] | Unspecified | | | Screen for compounds that inhibit polyglutamine induced protein aggregation (AGREG) [AID1604, Type: other] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screen for compounds that inhibit polyglutamine induced protein aggregation (AGREG) | | AID | 1604 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 21 | [SID8150002] | Unspecified | | | Screening of compounds showing protective effect against cell death induced by familial amyotrophic lateral sclerosis (FALS)-linked mutantsuperoxide dismutase 1 (SOD1) (ALSOD1) [AID1605, Type: other] | |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screening of compounds showing protective effect against cell death induced by familial amyotrophic lateral sclerosis (FALS)-linked mutantsuperoxide dismutase 1 (SOD1) (ALSOD1) | | AID | 1605 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 22 | [SID8150002] | Unspecified | | | Screen for compounds that correct neuronal dysfunction without cell death as induced by the expression of polyglutamine-expanded, N-terminal huntingtin in C. elegans mechanosensory neurons (HDELENEU) [AID1599, Type: other] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Screen for compounds that correct neuronal dysfunction without cell death as induced by the expression of polyglutamine-expanded, N-terminal huntingtin in C. elegans mechanosensory neurons (HDELENEU) | | AID | 1599 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 23 | [SID8150002] | Unspecified | | | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubU) [AID1593, Type: other] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubU) | | AID | 1593 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 24 | [SID8150002] | Unspecified | | | Assay to identify inhibitors of polyglutamine-induced caspase-3 activation (CASP3) [AID1583, Type: other] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 8150002 | | CID | 5280531 | | Outcome | Unspecified | | BioAssay | Assay to identify inhibitors of polyglutamine-induced caspase-3 activation (CASP3) | | AID | 1583 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 25 | [SID57260141] | Inactive | Potency | 18.526 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | Potency | 18.526 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | | AID | 504834 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 26 | [SID57260141] | Inactive | Potency | 50.1187 | qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS [AID624287, Type: confirmatory] | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | Potency | 50.1187 [uM] | | BioAssay | qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS | | AID | 624287 | | BioAssay type | confirmatory | | Target | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] | | PubMed | | | Data Table |  |
|
| 27 | [SID57260141] | Inactive | Potency | | qHTS for Antagonists of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS [AID624288, Type: confirmatory] | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Antagonists of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS | | AID | 624288 | | BioAssay type | confirmatory | | Target | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] | | PubMed | | | Data Table |  |
|
| 28 | [SID57260141] | Inactive | | | Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha [AID2650, Type: screening] | GSK3A gene product [Homo sapiens] [gi:49574532] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | | AID | 2650 | | BioAssay type | screening | | Target | GSK3A gene product [Homo sapiens] [gi:49574532] | | PubMed | | | Data Table |  |
|
| 29 | [SID57260141] | Inactive | | | Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha [AID2650, Type: screening] | GSK3A gene product [Homo sapiens] [gi:49574532] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of GSK-3 alpha | | AID | 2650 | | BioAssay type | screening | | Target | GSK3A gene product [Homo sapiens] [gi:49574532] | | PubMed | | | Data Table |  |
|
| 30 | [SID26748810] | Inactive | Potency | | Confirmation and Secondary Assay for Modulators of Hemoglobin Beta Chain Splicing at IVS2 705 locus [AID930, Type: confirmatory] | hemoglobin subunit beta [Homo sapiens] [gi:4504349] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 26748810 | | CID | 5280531 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Confirmation and Secondary Assay for Modulators of Hemoglobin Beta Chain Splicing at IVS2 705 locus | | AID | 930 | | BioAssay type | confirmatory | | Target | hemoglobin subunit beta [Homo sapiens] [gi:4504349] | | PubMed | | | Data Table |  |
|
| 31 | [SID26748810] | Inactive | Potency | | Confirmation and Secondary Assay for Modulators of Hemoglobin Beta Chain Splicing at IVS2 654 locus [AID910, Type: confirmatory] | hemoglobin subunit beta [Homo sapiens] [gi:4504349] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 26748810 | | CID | 5280531 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Confirmation and Secondary Assay for Modulators of Hemoglobin Beta Chain Splicing at IVS2 654 locus | | AID | 910 | | BioAssay type | confirmatory | | Target | hemoglobin subunit beta [Homo sapiens] [gi:4504349] | | PubMed | | | Data Table |  |
|
| 32 | [SID57260141] | Inactive | | | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID485270, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 485270 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 33 | [SID57260141] | Inactive | | | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID485270, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 485270 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 34 | [SID57260141] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID434989, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 434989 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 35 | [SID57260141] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID434989, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 434989 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
|
| 36 | [SID26748810] | Inactive | | | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Cytoprotection (ATP) [AID1471, Type: confirmatory] | huntingtin [Homo sapiens] [gi:90903231] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 26748810 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Cytoprotection (ATP) | | AID | 1471 | | BioAssay type | confirmatory | | Target | huntingtin [Homo sapiens] [gi:90903231] | | PubMed | | | Data Table |  |
|
| 37 | [SID26748810] | Inactive | | | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Cytoprotection (ATP) [AID1471, Type: confirmatory] | huntingtin [Homo sapiens] [gi:90903231] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 26748810 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Cytoprotection (ATP) | | AID | 1471 | | BioAssay type | confirmatory | | Target | huntingtin [Homo sapiens] [gi:90903231] | | PubMed | | | Data Table |  |
|
| 38 | [SID26748810] | Inactive | Potency | | 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. | 38 | | Structure |
| | Substance | | | SID | 26748810 | | CID | 5280531 | | Outcome | Inactive | | Potency | [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 |  |
|
| 39 | [SID26748810] | Inactive | Potency | | 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. | 39 | | Structure |
| | Substance | | | SID | 26748810 | | CID | 5280531 | | Outcome | Inactive | | Potency | [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 |  |
|
| 40 | [SID26748810] | Inactive | Potency | | 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. | 40 | | Structure |
| | Substance | | | SID | 26748810 | | CID | 5280531 | | Outcome | Inactive | | Potency | [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 |  |
|
| 41 | [SID57260141] | Inactive | | | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) [AID652257, Type: screening] | PRMT1 protein [Homo sapiens] [gi:32425330] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) | | AID | 652257 | | BioAssay type | screening | | Target | PRMT1 protein [Homo sapiens] [gi:32425330] | | PubMed | | | Data Table |  |
|
| 42 | [SID57260141] | Inactive | | | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) [AID652257, Type: screening] | PRMT1 protein [Homo sapiens] [gi:32425330] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) | | AID | 652257 | | BioAssay type | screening | | Target | PRMT1 protein [Homo sapiens] [gi:32425330] | | PubMed | | | Data Table |  |
|
| 43 | [SID57260141] | Inactive | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504692, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504692 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
|
| 44 | [SID57260141] | Inactive | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504692, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504692 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
|
| 45 | [SID57260141] | Inactive | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504692, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504692 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
|
| 46 | [SID57260141] | Inactive | | | Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504634, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504634 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
|
| 47 | [SID57260141] | Inactive | | | Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504634, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504634 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
|
| 48 | [SID57260141] | Inactive | | | Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504634, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Counterscreen for inverse agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based full-deck high throughput screening assay to identify inverse agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504634 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
|
| 49 | [SID57260141] | Inactive | | | Fluorescence polarization-based cell-based primary high throughput screening assay to identify activators of insulin-degrading enzyme (IDE) [AID493087, Type: screening] | IDE gene product [Homo sapiens] [gi:155969707] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based cell-based primary high throughput screening assay to identify activators of insulin-degrading enzyme (IDE) | | AID | 493087 | | BioAssay type | screening | | Target | IDE gene product [Homo sapiens] [gi:155969707] | | PubMed | | | Data Table |  |
|
| 50 | [SID57260141] | Inactive | | | Fluorescence polarization-based cell-based primary high throughput screening assay to identify inhibitors of insulin-degrading enzyme (IDE) [AID434962, Type: screening] | IDE gene product [Homo sapiens] [gi:155969707] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 57260141 | | CID | 5280531 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based cell-based primary high throughput screening assay to identify inhibitors of insulin-degrading enzyme (IDE) | | AID | 434962 | | BioAssay type | screening | | Target | IDE gene product [Homo sapiens] [gi:155969707] | | PubMed | | | Data Table |  |
|