| 1 | [SID7978064] | Unspecified | Potency | | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | 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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| 2 | [SID7978064] | Unspecified | Potency | | Activators of T cell receptors: qHTS campaign [AID504894, Type: confirmatory] | T cell receptor [Homo sapiens] [gi:553160] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | Activators of T cell receptors: qHTS campaign | | AID | 504894 | | BioAssay type | confirmatory | | Target | T cell receptor [Homo sapiens] [gi:553160] | | PubMed | | | Data Table |  |
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| 3 | [SID7978064] | 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. | 3 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | 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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| 4 | [SID7978064] | 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. | 4 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | 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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| 5 | [SID7978064] | Inactive | Potency | 19.9526 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 6 | [SID7978064] | Inactive | Potency | 19.9526 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 7 | [SID7978064] | Inactive | Potency | 28.1838 | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | | AID | 624417 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
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| 8 | [SID7978064] | Inactive | Potency | 28.1838 | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | | AID | 624417 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
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| 9 | [SID7978064] | Inactive | Potency | 89.1251 | qHTS for Inhibitors of WRN Helicase [AID651768, Type: confirmatory] | WRN [Homo sapiens] [gi:3719421] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | 89.1251 [uM] | | BioAssay | qHTS for Inhibitors of WRN Helicase | | AID | 651768 | | BioAssay type | confirmatory | | Target | WRN [Homo sapiens] [gi:3719421] | | PubMed | | | Data Table |  |
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| 10 | [SID7978064] | Inactive | | | HTS for 14-3-3 protein interaction modulators [AID422, Type: screening] | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide [Homo sapi [gi:21464101] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | HTS for 14-3-3 protein interaction modulators | | AID | 422 | | BioAssay type | screening | | Target | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide [Homo sapi [gi:21464101] | | PubMed | | | Data Table |  |
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| 11 | [SID7978064] | Inactive | | | 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. | 11 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | | AID | 463082 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 12 | [SID7978064] | Inactive | | | 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. | 12 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | | AID | 463082 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 13 | [SID7978064] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3) [AID588352, Type: screening] | nuclear receptor coactivator 3 isoform a [Homo sapiens] [gi:32307126] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3) | | AID | 588352 | | BioAssay type | screening | | Target | nuclear receptor coactivator 3 isoform a [Homo sapiens] [gi:32307126] | | PubMed | | | Data Table |  |
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| 14 | [SID7978064] | Inactive | | | HTS for BAP1 Enzyme inhibitors [AID436, Type: screening] | Ubiquitin carboxyl-terminal hydrolase BAP1 (BRCA1-associated protein 1) (Cerebral protein 6) [gi:68565074] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | HTS for BAP1 Enzyme inhibitors | | AID | 436 | | BioAssay type | screening | | Target | Ubiquitin carboxyl-terminal hydrolase BAP1 (BRCA1-associated protein 1) (Cerebral protein 6) [gi:68565074] | | PubMed | | | Data Table |  |
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| 15 | [SID7978064] | Inactive | | | Identification of inhibitors of RAD54 Measured in Biochemical System Using Plate Reader - 2159-01_Inhibitor_SinglePoint_HTS_Activity [AID602329, Type: screening] | RAD54L gene product [Homo sapiens] [gi:216548193] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Identification of inhibitors of RAD54 Measured in Biochemical System Using Plate Reader - 2159-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 602329 | | BioAssay type | screening | | Target | RAD54L gene product [Homo sapiens] [gi:216548193] | | PubMed | | | Data Table |  |
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| 16 | [SID7978064] | Inactive | | | 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. | 16 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | 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 |  |
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| 17 | [SID7978064] | Inactive | | | 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. | 17 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | 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 |  |
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| 18 | [SID7978064] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) [AID588354, Type: screening] | nuclear receptor coactivator 1 isoform 1 [Homo sapiens] [gi:22538455] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) | | AID | 588354 | | BioAssay type | screening | | Target | nuclear receptor coactivator 1 isoform 1 [Homo sapiens] [gi:22538455] | | PubMed | | | Data Table |  |
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| 19 | [SID7978064] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) [AID588354, Type: screening] | nuclear receptor coactivator 1 isoform 1 [Homo sapiens] [gi:22538455] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) | | AID | 588354 | | BioAssay type | screening | | Target | nuclear receptor coactivator 1 isoform 1 [Homo sapiens] [gi:22538455] | | PubMed | | | Data Table |  |
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| 20 | [SID7978064] | Inactive | | | Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1509, Type: screening] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1509 | | BioAssay type | screening | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
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| 21 | [SID7978064] | Inactive | | | Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1509, Type: screening] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary Cell-Based Assay to Identify Agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1509 | | BioAssay type | screening | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
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| 22 | [SID7978064] | Inactive | | | Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1510, Type: screening] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1510 | | BioAssay type | screening | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
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| 23 | [SID7978064] | Inactive | | | Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1510, Type: screening] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary Cell-Based Assay to Identify Antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1510 | | BioAssay type | screening | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
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| 24 | [SID7978064] | Inactive | | | uHTS for the identification of compounds that potentiate TRAIL-induced apoptosis of cancer cells [AID1443, Type: screening] | tumor necrosis factor ligand superfamily member 10 isoform 1 [Homo sapiens] [gi:4507593] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | uHTS for the identification of compounds that potentiate TRAIL-induced apoptosis of cancer cells | | AID | 1443 | | BioAssay type | screening | | Target | tumor necrosis factor ligand superfamily member 10 isoform 1 [Homo sapiens] [gi:4507593] | | PubMed | | | Data Table |  |
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| 25 | [SID7978064] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and the receptor-interacting serine-threonine kinase 2 (RIPK2) [AID624267, Type: screening] | RIPK2 gene product [Homo sapiens] [gi:4506537] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and the receptor-interacting serine-threonine kinase 2 (RIPK2) | | AID | 624267 | | BioAssay type | screening | | Target | RIPK2 gene product [Homo sapiens] [gi:4506537] | | PubMed | | | Data Table |  |
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| 26 | [SID7978064] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and the receptor-interacting serine-threonine kinase 2 (RIPK2) [AID624267, Type: screening] | RIPK2 gene product [Homo sapiens] [gi:4506537] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and the receptor-interacting serine-threonine kinase 2 (RIPK2) | | AID | 624267 | | BioAssay type | screening | | Target | RIPK2 gene product [Homo sapiens] [gi:4506537] | | PubMed | | | Data Table |  |
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| 27 | [SID7978064] | Inactive | | | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay [AID624354, Type: screening] | TNFRSF10B gene product [Homo sapiens] [gi:224494019] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay | | AID | 624354 | | BioAssay type | screening | | Target | TNFRSF10B gene product [Homo sapiens] [gi:224494019] | | PubMed | | | Data Table |  |
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| 28 | [SID7978064] | Inactive | | | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay [AID624354, Type: screening] | TNFRSF10B gene product [Homo sapiens] [gi:224494019] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay | | AID | 624354 | | BioAssay type | screening | | Target | TNFRSF10B gene product [Homo sapiens] [gi:224494019] | | PubMed | | | Data Table |  |
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| 29 | [SID7978064] | Inactive | | | Primary cell-based high-throughput screening assay to identify agonists of Galanin Receptor 2 (GALR2) [AID803, Type: screening] | Galanin receptor type 2 [gi:6016094] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay to identify agonists of Galanin Receptor 2 (GALR2) | | AID | 803 | | BioAssay type | screening | | Target | Galanin receptor type 2 [gi:6016094] | | PubMed | | | Data Table |  |
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| 30 | [SID7978064] | Inactive | | | Primary cell-based high-throughput screening assay to identify antagonists of Galanin Receptor 2 (GALR2) [AID828, Type: screening] | Galanin receptor type 2 [gi:6016094] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay to identify antagonists of Galanin Receptor 2 (GALR2) | | AID | 828 | | BioAssay type | screening | | Target | Galanin receptor type 2 [gi:6016094] | | PubMed | | | Data Table |  |
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| 31 | [SID7978064] | Inactive | | | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of Histone Deacetylase 3 [AID2718, Type: screening] | histone deacetylase 3 [Homo sapiens] [gi:13128862] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of Histone Deacetylase 3 | | AID | 2718 | | BioAssay type | screening | | Target | histone deacetylase 3 [Homo sapiens] [gi:13128862] | | PubMed | | | Data Table |  |
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| 32 | [SID7978064] | Inactive | | | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of Histone Deacetylase 3 [AID2718, Type: screening] | histone deacetylase 3 [Homo sapiens] [gi:13128862] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of Histone Deacetylase 3 | | AID | 2718 | | BioAssay type | screening | | Target | histone deacetylase 3 [Homo sapiens] [gi:13128862] | | PubMed | | | Data Table |  |
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| 33 | [SID7978064] | Inactive | | | Development of CDK5 inhibitors Measured in Biochemical System Using Plate Reader - 2083-01_Inhibitor_SinglePoint_HTS_Activity [AID488839, Type: screening] | Cyclin-dependent kinase 5, regulatory subunit 1 (p35) [Homo sapiens] [gi:20072248] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Development of CDK5 inhibitors Measured in Biochemical System Using Plate Reader - 2083-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 488839 | | BioAssay type | screening | | Target | Cyclin-dependent kinase 5, regulatory subunit 1 (p35) [Homo sapiens] [gi:20072248] | | PubMed | | | Data Table |  |
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| 34 | [SID7978064] | Inactive | | | Development of CDK5 inhibitors Measured in Biochemical System Using Plate Reader - 2083-01_Inhibitor_SinglePoint_HTS_Activity [AID488839, Type: screening] | Cyclin-dependent kinase 5, regulatory subunit 1 (p35) [Homo sapiens] [gi:20072248] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Development of CDK5 inhibitors Measured in Biochemical System Using Plate Reader - 2083-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 488839 | | BioAssay type | screening | | Target | Cyclin-dependent kinase 5, regulatory subunit 1 (p35) [Homo sapiens] [gi:20072248] | | PubMed | | | Data Table |  |
|
| 35 | [SID7978064] | Inactive | | | Development of CDK5 inhibitors Measured in Biochemical System Using Plate Reader - 2083-01_Inhibitor_SinglePoint_HTS_Activity [AID488839, Type: screening] | Cyclin-dependent kinase 5, regulatory subunit 1 (p35) [Homo sapiens] [gi:20072248] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Development of CDK5 inhibitors Measured in Biochemical System Using Plate Reader - 2083-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 488839 | | BioAssay type | screening | | Target | Cyclin-dependent kinase 5, regulatory subunit 1 (p35) [Homo sapiens] [gi:20072248] | | PubMed | | | Data Table |  |
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| 36 | [SID7978064] | Inactive | | | uHTS identification of inhibitors of cullin neddylation in a TR-FRET assay [AID651699, Type: screening] | NAE1 gene product [Homo sapiens] [gi:4502169] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | uHTS identification of inhibitors of cullin neddylation in a TR-FRET assay | | AID | 651699 | | BioAssay type | screening | | Target | NAE1 gene product [Homo sapiens] [gi:4502169] | | PubMed | | | Data Table |  |
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| 37 | [SID7978064] | Inactive | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
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| 38 | [SID7978064] | Inactive | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
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| 39 | [SID7978064] | Inactive | | | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen [AID449739, Type: screening] | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Inhibitors of Cav3 T-type Calcium Channels: Primary Screen | | AID | 449739 | | BioAssay type | screening | | Target | voltage-dependent T-type calcium channel subunit alpha-1H isoform a [Homo sapiens] [gi:53832009] | | PubMed | | | Data Table |  |
|
| 40 | [SID7978064] | Inactive | | | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide [AID686964, Type: screening] | Methyl-CpG binding domain protein 2 [Homo sapiens] [gi:21595776] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide | | AID | 686964 | | BioAssay type | screening | | Target | Methyl-CpG binding domain protein 2 [Homo sapiens] [gi:21595776] | | PubMed | | | Data Table |  |
|
| 41 | [SID7978064] | Inactive | Potency | | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter [AID463254, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter | | AID | 463254 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 42 | [SID7978064] | Inactive | Potency | | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter [AID463254, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter | | AID | 463254 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 43 | [SID7978064] | Inactive | Potency | | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a [AID927, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a | | AID | 927 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 44 | [SID7978064] | Inactive | Potency | | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a [AID927, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Ubiquitin-specific Protease USP2a | | AID | 927 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 45 | [SID7978064] | Inactive | | | uHTS identification of small molecule activators of alpha dystroglycan glycosylation [AID624168, Type: screening] | LARGE [Homo sapiens] [gi:47678551] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule activators of alpha dystroglycan glycosylation | | AID | 624168 | | BioAssay type | screening | | Target | LARGE [Homo sapiens] [gi:47678551] | | PubMed | | | Data Table |  |
|
| 46 | [SID7978064] | Inactive | IC50 | | Image-Based HTS for Selective Antagonists for GPR55 [AID2013, Type: confirmatory] | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Image-Based HTS for Selective Antagonists for GPR55 | | AID | 2013 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] | | PubMed | | | Data Table |  |
|
| 47 | [SID7978064] | Inactive | EC50 | | Image-based HTS for Selective Agonists of GPR55 [AID1961, Type: confirmatory] | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | EC50 | [uM] | | BioAssay | Image-based HTS for Selective Agonists of GPR55 | | AID | 1961 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] | | PubMed | | | Data Table |  |
|
| 48 | [SID7978064] | Inactive | | | Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) [AID736, Type: screening] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | | AID | 736 | | BioAssay type | screening | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 49 | [SID7978064] | Inactive | | | Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) [AID736, Type: screening] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | | AID | 736 | | BioAssay type | screening | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 50 | [SID7978064] | Inactive | | | Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) [AID736, Type: screening] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 7978064 | | CID | 9587136 | | Outcome | Inactive | | BioAssay | Primary Cell-Based High-Throughput Screening to Identify Antagonists of the Sphingosine 1-phosphate receptor 2 (S1P2) | | AID | 736 | | BioAssay type | screening | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|