| 1 | [SID7975695] | Active | | | Allosteric Modulators of D1 Receptors: Primary Screen [AID641, Type: screening] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Active | | BioAssay | Allosteric Modulators of D1 Receptors: Primary Screen | | AID | 641 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 2 | [SID7975695] | Active | | | Allosteric Modulators of D1 Receptors: Confirmation Screen [AID642, Type: other] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Active | | BioAssay | Allosteric Modulators of D1 Receptors: Confirmation Screen | | AID | 642 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 3 | [SID7975695] | Active | | | Primary cell-based high-throughput screening assay to measure PERK inhibition [AID1416, Type: screening] | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay to measure PERK inhibition | | AID | 1416 | | BioAssay type | screening | | Target | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] | | PubMed | | | Data Table |  |
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| 4 | [SID7975695] | Active | | | Primary cell-based high-throughput screening assay to measure PERK inhibition [AID1416, Type: screening] | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay to measure PERK inhibition | | AID | 1416 | | BioAssay type | screening | | Target | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] | | PubMed | | | Data Table |  |
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| 5 | [SID7975695] | Active | | | Allosteric Modulators of D1 Receptors: Secondary Assay 2 [AID647, Type: other] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Active | | BioAssay | Allosteric Modulators of D1 Receptors: Secondary Assay 2 | | AID | 647 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 6 | [SID7975695] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 7 | [SID7975695] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 8 | [SID7975695] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 9 | [SID7975695] | Unspecified | Potency | | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Unspecified | | Potency | [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 |  |
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| 10 | [SID7975695] | 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 | 7975695 | | CID | 686254 | | 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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| 11 | [SID7975695] | 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 | 7975695 | | CID | 686254 | | 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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| 12 | [SID7975695] | Inactive | EC50 | 55.7 | Dose response cell-based high-throughput screening assay to measure PERK inhibition [AID1522, Type: confirmatory] | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | EC50 | 55.7 [uM] | | BioAssay | Dose response cell-based high-throughput screening assay to measure PERK inhibition | | AID | 1522 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] | | PubMed | | | Data Table |  |
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| 13 | [SID7975695] | Inactive | EC50 | 55.7 | Dose response cell-based high-throughput screening assay to measure PERK inhibition [AID1522, Type: confirmatory] | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | EC50 | 55.7 [uM] | | BioAssay | Dose response cell-based high-throughput screening assay to measure PERK inhibition | | AID | 1522 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] | | PubMed | | | Data Table |  |
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| 14 | [SID7975695] | Inactive | EC50 | 55.7 | Counterscreen assay for PERK inhibitors: Dose response cell-based high throughput screening assay to measure inhibition of PERK at 6 hours [AID1528, Type: confirmatory] | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | EC50 | 55.7 [uM] | | BioAssay | Counterscreen assay for PERK inhibitors: Dose response cell-based high throughput screening assay to measure inhibition of PERK at 6 hours | | AID | 1528 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] | | PubMed | | | Data Table |  |
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| 15 | [SID7975695] | Inactive | EC50 | 55.7 | Counterscreen assay for PERK inhibitors: Dose response cell-based high throughput screening assay to measure inhibition of PERK at 6 hours [AID1528, Type: confirmatory] | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | EC50 | 55.7 [uM] | | BioAssay | Counterscreen assay for PERK inhibitors: Dose response cell-based high throughput screening assay to measure inhibition of PERK at 6 hours | | AID | 1528 | | BioAssay type | confirmatory | | Target | eukaryotic translation initiation factor 2-alpha kinase 3 [Homo sapiens] [gi:134304838] | | PubMed | | | Data Table |  |
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| 16 | [SID7975695] | Inactive | Potency | 89.1251 | 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. | 16 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | Potency | 89.1251 [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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| 17 | [SID7975695] | Inactive | Potency | | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
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| 18 | [SID7975695] | Inactive | Potency | | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
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| 19 | [SID7975695] | Inactive | IC50 | | HTS discovery of chemical inhibitors of anti-apoptotic protein Bfl-1 [AID432, Type: confirmatory] | Bcl2a1a gene product [Mus musculus] [gi:11024684] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | HTS discovery of chemical inhibitors of anti-apoptotic protein Bfl-1 | | AID | 432 | | BioAssay type | confirmatory | | Target | Bcl2a1a gene product [Mus musculus] [gi:11024684] | | PubMed | | | Data Table |  |
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| 20 | [SID7975695] | Inactive | | | HTS for small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress [AID2732, Type: screening] | Ddit3 gene product [Mus musculus] [gi:160707929] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | HTS for small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress | | AID | 2732 | | BioAssay type | screening | | Target | Ddit3 gene product [Mus musculus] [gi:160707929] | | PubMed | | | Data Table |  |
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| 21 | [SID7975695] | Inactive | | | uHTS for Small Molecule Inhibitors of Eukaryotic Translation Initiation [AID782, Type: screening] | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | uHTS for Small Molecule Inhibitors of Eukaryotic Translation Initiation | | AID | 782 | | BioAssay type | screening | | Target | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] | | PubMed | | | Data Table |  |
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| 22 | [SID7975695] | Inactive | | | uHTS for Small Molecule Inhibitors of Eukaryotic Translation Initiation [AID782, Type: screening] | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | uHTS for Small Molecule Inhibitors of Eukaryotic Translation Initiation | | AID | 782 | | BioAssay type | screening | | Target | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] | | PubMed | | | Data Table |  |
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| 23 | [SID7975695] | Inactive | | | Activator for delta FosB/delta FosB homodimer Measured in Biochemical System Using Plate Reader - 2072-01_Activator_SinglePoint_HTS_Activity [AID493131, Type: screening] | protein fosB [Mus musculus] [gi:6679827] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Activator for delta FosB/delta FosB homodimer Measured in Biochemical System Using Plate Reader - 2072-01_Activator_SinglePoint_HTS_Activity | | AID | 493131 | | BioAssay type | screening | | Target | protein fosB [Mus musculus] [gi:6679827] | | PubMed | | | Data Table |  |
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| 24 | [SID7975695] | Inactive | | | uHTS identification of Gli-Sufu Antagonists in a luminescence reporter assay [AID588413, Type: screening] | Gli1 [Mus musculus] [gi:6009644] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | uHTS identification of Gli-Sufu Antagonists in a luminescence reporter assay | | AID | 588413 | | BioAssay type | screening | | Target | Gli1 [Mus musculus] [gi:6009644] | | PubMed | | | Data Table |  |
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| 25 | [SID7975695] | Inactive | | | uHTS identification of Gli-Sufu Antagonists in a luminescence reporter assay [AID588413, Type: screening] | Gli1 [Mus musculus] [gi:6009644] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | uHTS identification of Gli-Sufu Antagonists in a luminescence reporter assay | | AID | 588413 | | BioAssay type | screening | | Target | Gli1 [Mus musculus] [gi:6009644] | | PubMed | | | Data Table |  |
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| 26 | [SID7975695] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1). [AID2098, Type: screening] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1). | | AID | 2098 | | BioAssay type | screening | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
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| 27 | [SID7975695] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1). [AID2098, Type: screening] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1). | | AID | 2098 | | BioAssay type | screening | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
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| 28 | [SID7975695] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) [AID624169, Type: screening] | Htr2a gene product [Mus musculus] [gi:27753985] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | | AID | 624169 | | BioAssay type | screening | | Target | Htr2a gene product [Mus musculus] [gi:27753985] | | PubMed | | | Data Table |  |
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| 29 | [SID7975695] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) [AID624169, Type: screening] | Htr2a gene product [Mus musculus] [gi:27753985] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | | AID | 624169 | | BioAssay type | screening | | Target | Htr2a gene product [Mus musculus] [gi:27753985] | | PubMed | | | Data Table |  |
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| 30 | [SID7975695] | Inactive | | | HTS for developing T Cell Immune Modulators [AID2052, Type: screening] | integrin alpha-L [Mus musculus] [gi:124486680] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | HTS for developing T Cell Immune Modulators | | AID | 2052 | | BioAssay type | screening | | Target | integrin alpha-L [Mus musculus] [gi:124486680] | | PubMed | | | Data Table |  |
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| 31 | [SID7975695] | Inactive | | | HTS for developing T Cell Immune Modulators [AID2052, Type: screening] | integrin alpha-L [Mus musculus] [gi:124486680] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | HTS for developing T Cell Immune Modulators | | AID | 2052 | | BioAssay type | screening | | Target | integrin alpha-L [Mus musculus] [gi:124486680] | | PubMed | | | Data Table |  |
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| 32 | [SID7975695] | Inactive | | | HTS for developing T Cell Immune Modulators [AID2052, Type: screening] | integrin alpha-L [Mus musculus] [gi:124486680] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | HTS for developing T Cell Immune Modulators | | AID | 2052 | | BioAssay type | screening | | Target | integrin alpha-L [Mus musculus] [gi:124486680] | | PubMed | | | Data Table |  |
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| 33 | [SID7975695] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 [AID1672, Type: screening] | inward rectifier potassium channel 2 [Mus musculus] [gi:6680530] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | | AID | 1672 | | BioAssay type | screening | | Target | inward rectifier potassium channel 2 [Mus musculus] [gi:6680530] | | PubMed | | | Data Table |  |
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| 34 | [SID7975695] | Inactive | IC50 | | Fluorescence for the identification of compounds that decrease p/CIP protein stability [AID1984, Type: confirmatory] | nuclear receptor coactivator 3 [Mus musculus] [gi:118026946] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Fluorescence for the identification of compounds that decrease p/CIP protein stability | | AID | 1984 | | BioAssay type | confirmatory | | Target | nuclear receptor coactivator 3 [Mus musculus] [gi:118026946] | | PubMed | | | Data Table |  |
|
| 35 | [SID7975695] | Inactive | | | Fluorescence polarization-based biochemical primary high throughput screening assay to identify activators of the Protein Kinase A-R1A (PKA-R1A) complex [AID504707, Type: screening] | cAMP-dependent protein kinase catalytic subunit beta isoform 1 [Mus musculus] [gi:6755076] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based biochemical primary high throughput screening assay to identify activators of the Protein Kinase A-R1A (PKA-R1A) complex | | AID | 504707 | | BioAssay type | screening | | Target | cAMP-dependent protein kinase catalytic subunit beta isoform 1 [Mus musculus] [gi:6755076] | | PubMed | | | Data Table |  |
|
| 36 | [SID7975695] | Inactive | Potency | | qHTS for Inhibitors of Cell Surface uPA Generation [AID540303, Type: confirmatory] | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Cell Surface uPA Generation | | AID | 540303 | | BioAssay type | confirmatory | | Target | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] | | PubMed | | | Data Table |  |
|
| 37 | [SID7975695] | Inactive | Potency | | qHTS for Inhibitors of Cell Surface uPA Generation [AID540303, Type: confirmatory] | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Cell Surface uPA Generation | | AID | 540303 | | BioAssay type | confirmatory | | Target | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] | | PubMed | | | Data Table |  |
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| 38 | [SID7975695] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) [AID2751, Type: screening] | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) | | AID | 2751 | | BioAssay type | screening | | Target | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] | | PubMed | | | Data Table |  |
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| 39 | [SID7975695] | Inactive | | | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity [AID504523, Type: screening] | KEAP1 gene product [Homo sapiens] [gi:45269145] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 504523 | | BioAssay type | screening | | Target | KEAP1 gene product [Homo sapiens] [gi:45269145] | | PubMed | | | Data Table |  |
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| 40 | [SID7975695] | Inactive | | | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity [AID504523, Type: screening] | KEAP1 gene product [Homo sapiens] [gi:45269145] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 504523 | | BioAssay type | screening | | Target | KEAP1 gene product [Homo sapiens] [gi:45269145] | | PubMed | | | Data Table |  |
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| 41 | [SID7975695] | Inactive | | | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). [AID2300, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). | | AID | 2300 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
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| 42 | [SID7975695] | Inactive | | | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). [AID2300, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). | | AID | 2300 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
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| 43 | [SID7975695] | Inactive | | | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). [AID2300, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). | | AID | 2300 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
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| 44 | [SID7975695] | Inactive | | | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) [AID602229, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | | AID | 602229 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
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| 45 | [SID7975695] | Inactive | | | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) [AID602229, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | | AID | 602229 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
|
| 46 | [SID7975695] | Inactive | | | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) [AID602229, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | | AID | 602229 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
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| 47 | [SID7975695] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B. [AID951, Type: screening] | Bcl-2-like protein 10 [gi:23396469] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B. | | AID | 951 | | BioAssay type | screening | | Target | Bcl-2-like protein 10 [gi:23396469] | | PubMed | | | Data Table |  |
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| 48 | [SID7975695] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B. [AID951, Type: screening] | Bcl-2-like protein 10 [gi:23396469] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B. | | AID | 951 | | BioAssay type | screening | | Target | Bcl-2-like protein 10 [gi:23396469] | | PubMed | | | Data Table |  |
|
| 49 | [SID7975695] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B. [AID951, Type: screening] | Bcl-2-like protein 10 [gi:23396469] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B. | | AID | 951 | | BioAssay type | screening | | Target | Bcl-2-like protein 10 [gi:23396469] | | PubMed | | | Data Table |  |
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| 50 | [SID7975695] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 7975695 | | CID | 686254 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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