| 1 | [SID49648713] | Active | IC50 | 1.598 | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in screening - selectivity counter screen assays - Set 2 [AID651549_3, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | IC50 | 1.598 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in screening - selectivity counter screen assays - Set 2 | | AID | 651549 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
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| 2 | [SID49648713] | Active | AbsAC35_uM | 2.85 | Counterscreen for inhibitors of NLG for Luciferase Activators Measured in Cell-Based System Using Plate Reader - 2146-03_Inhibitor_Dose_CherryPick_Activity [AID624404, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | AbsAC35_uM | 2.85 [uM] | | BioAssay | Counterscreen for inhibitors of NLG for Luciferase Activators Measured in Cell-Based System Using Plate Reader - 2146-03_Inhibitor_Dose_CherryPick_Activity | | AID | 624404 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 3 | [SID49648713] | Active | Potency | 5.1735 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 5.1735 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
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| 4 | [SID49648713] | Active | Potency | 5.1735 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 5.1735 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
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| 5 | [SID49648713] | Active | Potency | 5.1735 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 5.1735 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
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| 6 | [SID49648713] | Active | Potency | 5.1735 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 5.1735 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
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| 7 | [SID49648713] | Active | IC50 | 6.509 | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in screening - selectivity counter screen assays - Set 2 [AID651549_1, Type: confirmatory] | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | IC50 | 6.509 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in screening - selectivity counter screen assays - Set 2 | | AID | 651549 | | BioAssay type | confirmatory | | Target | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] | | PubMed | | | Data Table |  |
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| 8 | [SID49648713] | Active | Potency | 10 | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen [AID588856, Type: confirmatory] | |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen | | AID | 588856 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 9 | [SID49648713] | Active | CC50 | 13.5 | A Cell Based Secondary Assay To Explore Cytotoxicity of West Nile Virus Anti-Viral Hit Compounds [AID1650, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | CC50 | 13.5 [uM] | | BioAssay | A Cell Based Secondary Assay To Explore Cytotoxicity of West Nile Virus Anti-Viral Hit Compounds | | AID | 1650 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 10 | [SID49648713] | Active | Potency | 14.575 | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 [AID504467, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 14.575 [uM] | | BioAssay | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 | | AID | 504467 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
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| 11 | [SID49648713] | Active | Potency | 14.581 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line [AID686971, Type: confirmatory] | |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 14.581 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line | | AID | 686971 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 12 | [SID49648713] | Active | CC50 | 18.54 | Vero 76 Cytoxicity Assay for VEEV Compounds [AID588719, Type: confirmatory] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | CC50 | 18.54 [uM] | | BioAssay | Vero 76 Cytoxicity Assay for VEEV Compounds | | AID | 588719 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 13 | [SID49648713] | Active | Potency | 25.929 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line [AID686970, Type: confirmatory] | IDH1 [Homo sapiens] [gi:49168486] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | Potency | 25.929 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line | | AID | 686970 | | BioAssay type | confirmatory | | Target | IDH1 [Homo sapiens] [gi:49168486] | | PubMed | | | Data Table |  |
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| 14 | [SID49648713] | Active | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors [AID1813, Type: screening] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors | | AID | 1813 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 15 | [SID49648713] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) [AID652017, Type: screening] | |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) | | AID | 652017 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 16 | [SID49648713] | Active | | | uHTS identification of modulators of interaction between CendR and NRP-1 using Fluorescence Polarization assay [AID602438, Type: screening] | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | uHTS identification of modulators of interaction between CendR and NRP-1 using Fluorescence Polarization assay | | AID | 602438 | | BioAssay type | screening | | Target | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] | | PubMed | | | Data Table |  |
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| 17 | [SID49648713] | Active | | | Fluorescence-based cell-based primary high throughput confirmation assay to identify antagonists of the Galanin Receptor 3 (GalR3) [AID652245, Type: screening] | |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput confirmation assay to identify antagonists of the Galanin Receptor 3 (GalR3) | | AID | 652245 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 18 | [SID49648713] | Active | | | Counterscreen for antagonists of the galanin Receptor 3 (GalR3): Fluorescence-based cell-based high throughput screening assay to identify non specific agonists of the parental HEK-CNG cells [AID652268, Type: screening] | |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Counterscreen for antagonists of the galanin Receptor 3 (GalR3): Fluorescence-based cell-based high throughput screening assay to identify non specific agonists of the parental HEK-CNG cells | | AID | 652268 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 19 | [SID49648713] | Active | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504905, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504905 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
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| 20 | [SID49648713] | Active | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504905, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504905 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
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| 21 | [SID49648713] | Active | | | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) [AID504905, Type: screening] | HTR5A gene product [Homo sapiens] [gi:13236497] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Counterscreen for agonists of OPRM1-OPRD1 heterodimerization: luminescence-based cell-based high throughput screening assay to identify agonists of 5-hydroxytryptamine (serotonin) 5A receptor (HTR5A) | | AID | 504905 | | BioAssay type | screening | | Target | HTR5A gene product [Homo sapiens] [gi:13236497] | | PubMed | | | Data Table |  |
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| 22 | [SID49648713] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R [AID540308, Type: screening] | melanocortin receptor 4 [Homo sapiens] [gi:119508433] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | | AID | 540308 | | BioAssay type | screening | | Target | melanocortin receptor 4 [Homo sapiens] [gi:119508433] | | PubMed | | | Data Table |  |
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| 23 | [SID49648713] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R [AID540308, Type: screening] | melanocortin receptor 4 [Homo sapiens] [gi:119508433] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify biased ligands of the melanocortin 4 receptor (MC4R): agonists of MC4R | | AID | 540308 | | BioAssay type | screening | | Target | melanocortin receptor 4 [Homo sapiens] [gi:119508433] | | PubMed | | | Data Table |  |
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| 24 | [SID49648713] | Active | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_1, Type: confirmatory] | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] | | PubMed | | | Data Table |  |
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| 25 | [SID49648713] | Active | EC50 | | uHTS luminescence assay for the identification of compounds that inhibit NOD2 [AID1566, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | EC50 | [uM] | | BioAssay | uHTS luminescence assay for the identification of compounds that inhibit NOD2 | | AID | 1566 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] | | PubMed | | | Data Table |  |
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| 26 | [SID49648713] | Active | EC50 | | uHTS luminescence assay for the identification of compounds that inhibit NOD2 [AID1566, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | EC50 | [uM] | | BioAssay | uHTS luminescence assay for the identification of compounds that inhibit NOD2 | | AID | 1566 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] | | PubMed | | | Data Table |  |
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| 27 | [SID49648713] | Active | EC50 | | uHTS luminescence assay for the identification of compounds that inhibit NOD2 [AID1566, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | EC50 | [uM] | | BioAssay | uHTS luminescence assay for the identification of compounds that inhibit NOD2 | | AID | 1566 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] | | PubMed | | | Data Table |  |
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| 28 | [SID49648713] | Active | | | 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. | 28 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | 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 |  |
|
| 29 | [SID49648713] | Active | | | 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. | 29 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | 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 |  |
|
| 30 | [SID49648713] | Active | | | 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. | 30 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | 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 |  |
|
| 31 | [SID49648713] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID504326, Type: screening] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 504326 | | BioAssay type | screening | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
|
| 32 | [SID49648713] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID504326, Type: screening] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 504326 | | BioAssay type | screening | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
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| 33 | [SID49648713] | Active | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) [AID651719, Type: screening] | GALR3 gene product [Homo sapiens] [gi:4503907] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) | | AID | 651719 | | BioAssay type | screening | | Target | GALR3 gene product [Homo sapiens] [gi:4503907] | | PubMed | | | Data Table |  |
|
| 34 | [SID49648713] | Active | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) [AID651719, Type: screening] | GALR3 gene product [Homo sapiens] [gi:4503907] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) | | AID | 651719 | | BioAssay type | screening | | Target | GALR3 gene product [Homo sapiens] [gi:4503907] | | PubMed | | | Data Table |  |
|
| 35 | [SID49648713] | Active | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_4, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 36 | [SID49648713] | Active | | | HTS Assay for Peg3 Promoter Inhibitors [AID588405, Type: screening] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | HTS Assay for Peg3 Promoter Inhibitors | | AID | 588405 | | BioAssay type | screening | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 37 | [SID49648713] | Active | | | Single concentration confirmation of uHTS hits for Peg3 Promoter Inhibitors via a luciferase reporter assay [AID602417, Type: screening] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS hits for Peg3 Promoter Inhibitors via a luciferase reporter assay | | AID | 602417 | | BioAssay type | screening | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 38 | [SID49648713] | Unspecified | IC50 | 95 | Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay [AID651650_2, Type: confirmatory] | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | 95 [uM] | | BioAssay | Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay | | AID | 651650 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] | | PubMed | | | Data Table |  |
|
| 39 | [SID49648713] | Unspecified | IC50 | 95 | Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay [AID651650_3, Type: confirmatory] | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | 95 [uM] | | BioAssay | Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay | | AID | 651650 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] | | PubMed | | | Data Table |  |
|
| 40 | [SID49648713] | Unspecified | IC50 | 100 | Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay [AID651650_5, Type: confirmatory] | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | 100 [uM] | | BioAssay | Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay | | AID | 651650 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] | | PubMed | | | Data Table |  |
|
| 41 | [SID49648713] | Unspecified | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_2, Type: confirmatory] | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] | | PubMed | | | Data Table |  |
|
| 42 | [SID49648713] | Unspecified | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_3, Type: confirmatory] | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Glyceraldehyde-3-phosphate dehydrogenase [gi:120649] | | PubMed | | | Data Table |  |
|
| 43 | [SID49648713] | 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. | 43 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | 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 |  |
|
| 44 | [SID49648713] | 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. | 44 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | 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 |  |
|
| 45 | [SID49648713] | Unspecified | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_8, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 46 | [SID49648713] | Unspecified | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_9, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 47 | [SID49648713] | Unspecified | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_5, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 48 | [SID49648713] | Unspecified | IC50 | | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167_6, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Unspecified | | IC50 | [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 49 | [SID49648713] | Inactive | IC50 | 10.4 | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay [AID624167, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Inactive | | IC50 | 10.4 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in a screening assay | | AID | 624167 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|
| 50 | [SID49648713] | Inactive | IC50 | 11.062 | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in screening - selectivity counter screen assays - Set 2 [AID651549_4, Type: confirmatory] | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 49648713 | | CID | 16396239 | | Outcome | Inactive | | IC50 | 11.062 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule Peg3 Promoter Inhibitor hits in screening - selectivity counter screen assays - Set 2 | | AID | 651549 | | BioAssay type | confirmatory | | Target | Ppp1r15a gene product [Rattus norvegicus] [gi:78486550] | | PubMed | | | Data Table |  |
|