| 1 | [SID24786359] | Active | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) [AID588852, Type: screening] | CHRM1 gene product [Homo sapiens] [gi:37622910] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | | AID | 588852 | | BioAssay type | screening | | Target | CHRM1 gene product [Homo sapiens] [gi:37622910] | | PubMed | | | Data Table |  |
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| 2 | [SID24786359] | Active | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) [AID588852, Type: screening] | CHRM1 gene product [Homo sapiens] [gi:37622910] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the human M1 muscarinic receptor (CHRM1) | | AID | 588852 | | BioAssay type | screening | | Target | CHRM1 gene product [Homo sapiens] [gi:37622910] | | PubMed | | | Data Table |  |
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| 3 | [SID24786359] | 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 | 24786359 | | CID | 5663297 | | 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 |  |
|
| 4 | [SID24786359] | 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 | 24786359 | | CID | 5663297 | | 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 | [SID24786359] | Inactive | Potency | 25.1189 | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction [AID624246, Type: confirmatory] | ERG gene product [Homo sapiens] [gi:343478176] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | 25.1189 [uM] | | BioAssay | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction | | AID | 624246 | | BioAssay type | confirmatory | | Target | ERG gene product [Homo sapiens] [gi:343478176] | | PubMed | | | Data Table |  |
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| 6 | [SID24786359] | Inactive | Potency | 25.1189 | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction [AID624246, Type: confirmatory] | ERG gene product [Homo sapiens] [gi:343478176] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | 25.1189 [uM] | | BioAssay | qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction | | AID | 624246 | | BioAssay type | confirmatory | | Target | ERG gene product [Homo sapiens] [gi:343478176] | | PubMed | | | Data Table |  |
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| 7 | [SID24786359] | Inactive | Potency | 79.4328 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | 79.4328 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 8 | [SID24786359] | Inactive | Potency | 79.4328 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | 79.4328 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 9 | [SID24786359] | Inactive | Potency | 79.4328 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | 79.4328 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 10 | [SID24786359] | Inactive | Potency | 79.4328 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | 79.4328 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 11 | [SID24786359] | Inactive | | | HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 [AID540275, Type: screening] | TRPV1 gene product [Homo sapiens] [gi:74315350] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | | AID | 540275 | | BioAssay type | screening | | Target | TRPV1 gene product [Homo sapiens] [gi:74315350] | | PubMed | | | Data Table |  |
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| 12 | [SID24786359] | Inactive | | | HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 [AID540275, Type: screening] | TRPV1 gene product [Homo sapiens] [gi:74315350] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | HTS Assay for Compounds that Act as Agonists of the Vanilloid Receptor 1 | | AID | 540275 | | BioAssay type | screening | | Target | TRPV1 gene product [Homo sapiens] [gi:74315350] | | PubMed | | | Data Table |  |
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| 13 | [SID24786359] | Inactive | | | HTS Assay for Compounds that Act as Potentiators of the Vanilloid Receptor 1 [AID540277, Type: screening] | TRPV1 gene product [Homo sapiens] [gi:74315350] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | HTS Assay for Compounds that Act as Potentiators of the Vanilloid Receptor 1 | | AID | 540277 | | BioAssay type | screening | | Target | TRPV1 gene product [Homo sapiens] [gi:74315350] | | PubMed | | | Data Table |  |
|
| 14 | [SID24786359] | Inactive | | | HTS Assay for Compounds that Act as Potentiators of the Vanilloid Receptor 1 [AID540277, Type: screening] | TRPV1 gene product [Homo sapiens] [gi:74315350] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | HTS Assay for Compounds that Act as Potentiators of the Vanilloid Receptor 1 | | AID | 540277 | | BioAssay type | screening | | Target | TRPV1 gene product [Homo sapiens] [gi:74315350] | | PubMed | | | Data Table |  |
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| 15 | [SID24786359] | Inactive | IC50 | | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) [AID2012, Type: confirmatory] | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) | | AID | 2012 | | BioAssay type | confirmatory | | Target | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] | | PubMed | | | Data Table |  |
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| 16 | [SID24786359] | Inactive | | | Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation [AID1321, Type: screening] | WEE1 homolog (S. pombe) [Homo sapiens] [gi:47123300] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation | | AID | 1321 | | BioAssay type | screening | | Target | WEE1 homolog (S. pombe) [Homo sapiens] [gi:47123300] | | PubMed | | | Data Table |  |
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| 17 | [SID24786359] | Inactive | | | Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation [AID1321, Type: screening] | WEE1 homolog (S. pombe) [Homo sapiens] [gi:47123300] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation | | AID | 1321 | | BioAssay type | screening | | Target | WEE1 homolog (S. pombe) [Homo sapiens] [gi:47123300] | | PubMed | | | Data Table |  |
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| 18 | [SID24786359] | Inactive | | | Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation [AID1321, Type: screening] | WEE1 homolog (S. pombe) [Homo sapiens] [gi:47123300] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Primary Cell-based High Throughput Screening Assay for Inhibitors of Wee1 Degradation | | AID | 1321 | | BioAssay type | screening | | Target | WEE1 homolog (S. pombe) [Homo sapiens] [gi:47123300] | | PubMed | | | Data Table |  |
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| 19 | [SID24786359] | Inactive | Potency | | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase [AID1631, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1631 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 20 | [SID24786359] | Inactive | Potency | | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase [AID1631, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1631 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 21 | [SID24786359] | Inactive | Potency | | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase [AID1631, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1631 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
|
| 22 | [SID24786359] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 23 | [SID24786359] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
|
| 24 | [SID24786359] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 25 | [SID24786359] | Inactive | IC50 | | uHTS identification of small molecule antagonists of the binding of Siah-1 and a peptide ligand via a fluorescence polarization assay. [AID1817, Type: confirmatory] | plectin 1 [Homo sapiens] [gi:40849930] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | uHTS identification of small molecule antagonists of the binding of Siah-1 and a peptide ligand via a fluorescence polarization assay. | | AID | 1817 | | BioAssay type | confirmatory | | Target | plectin 1 [Homo sapiens] [gi:40849930] | | PubMed | | | Data Table |  |
|
| 26 | [SID24786359] | Inactive | Potency | | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 27 | [SID24786359] | Inactive | Potency | | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 28 | [SID24786359] | Inactive | Potency | | qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2 [AID488837, Type: confirmatory] | eyes absent homolog 2 isoform a [Homo sapiens] [gi:26667227] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2 | | AID | 488837 | | BioAssay type | confirmatory | | Target | eyes absent homolog 2 isoform a [Homo sapiens] [gi:26667227] | | PubMed | | | Data Table |  |
|
| 29 | [SID24786359] | Inactive | | | Factor XIa 1536 HTS [AID798, Type: screening] | coagulation factor XI [gi:180352] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Factor XIa 1536 HTS | | AID | 798 | | BioAssay type | screening | | Target | coagulation factor XI [gi:180352] | | PubMed | | | Data Table |  |
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| 30 | [SID24786359] | Inactive | | | Factor XIa 1536 HTS [AID798, Type: screening] | coagulation factor XI [gi:180352] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Factor XIa 1536 HTS | | AID | 798 | | BioAssay type | screening | | Target | coagulation factor XI [gi:180352] | | PubMed | | | Data Table |  |
|
| 31 | [SID24786359] | Inactive | | | Factor XIIa 1536 HTS [AID800, Type: screening] | Coagulation factor XII [gi:317373446] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Factor XIIa 1536 HTS | | AID | 800 | | BioAssay type | screening | | Target | Coagulation factor XII [gi:317373446] | | PubMed | | | Data Table |  |
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| 32 | [SID24786359] | Inactive | | | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay [AID602261, Type: screening] | FASN gene product [Homo sapiens] [gi:41872631] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay | | AID | 602261 | | BioAssay type | screening | | Target | FASN gene product [Homo sapiens] [gi:41872631] | | PubMed | | | Data Table |  |
|
| 33 | [SID24786359] | Inactive | | | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay [AID602261, Type: screening] | FASN gene product [Homo sapiens] [gi:41872631] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay | | AID | 602261 | | BioAssay type | screening | | Target | FASN gene product [Homo sapiens] [gi:41872631] | | PubMed | | | Data Table |  |
|
| 34 | [SID24786359] | Inactive | | | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay [AID602261, Type: screening] | FASN gene product [Homo sapiens] [gi:41872631] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of the thioesterase domain of fatty acid synthase via a fluorescence intensity assay | | AID | 602261 | | BioAssay type | screening | | Target | FASN gene product [Homo sapiens] [gi:41872631] | | PubMed | | | Data Table |  |
|
| 35 | [SID24786359] | Inactive | | | A yeast HTS for caloric restriction mimetics that inhibit age-related superoxide [AID2690, Type: screening] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | A yeast HTS for caloric restriction mimetics that inhibit age-related superoxide | | AID | 2690 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 36 | [SID24786359] | Inactive | | | Luminescence Microorganism Primary HTS to Identify Inhibitors of the SUMOylation Pathway Using a Temperature Sensitive Growth Reversal Mutant Mot1-301 [AID2716, Type: screening] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Luminescence Microorganism Primary HTS to Identify Inhibitors of the SUMOylation Pathway Using a Temperature Sensitive Growth Reversal Mutant Mot1-301 | | AID | 2716 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 37 | [SID24786359] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Cancer Stem Cells [AID2717, Type: screening] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Cancer Stem Cells | | AID | 2717 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 38 | [SID24786359] | Inactive | IC90 | | Screen to Identify Novel Compounds That Sensitize Mycobacterium Tuberculosis to Beta-lactam Antibiotics [AID434955, Type: confirmatory] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | IC90 | [uM] | | BioAssay | Screen to Identify Novel Compounds That Sensitize Mycobacterium Tuberculosis to Beta-lactam Antibiotics | | AID | 434955 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 39 | [SID24786359] | Inactive | | | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation [AID435003, Type: screening] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation | | AID | 435003 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 40 | [SID24786359] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Beta Cell Apoptosis. [AID435005, Type: screening] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Beta Cell Apoptosis. | | AID | 435005 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 41 | [SID24786359] | Inactive | | | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation [AID435022, Type: screening] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation | | AID | 435022 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 42 | [SID24786359] | Inactive | | | Counterscreen for inhibitors of AddAB: absorbance-based bacterial cell-based high throughput screening assay to identify inhibitors of bacterial viability [AID449728, Type: screening] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Counterscreen for inhibitors of AddAB: absorbance-based bacterial cell-based high throughput screening assay to identify inhibitors of bacterial viability | | AID | 449728 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 43 | [SID24786359] | Inactive | | | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Inhibitor_SinglePoint_HTS_Activity [AID488896, Type: screening] | Scarb1 gene product [Mus musculus] [gi:14389423] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 488896 | | BioAssay type | screening | | Target | Scarb1 gene product [Mus musculus] [gi:14389423] | | PubMed | | | Data Table |  |
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| 44 | [SID24786359] | Inactive | | | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity [AID504775, Type: screening] | Scarb1 gene product [Mus musculus] [gi:14389423] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity | | AID | 504775 | | BioAssay type | screening | | Target | Scarb1 gene product [Mus musculus] [gi:14389423] | | PubMed | | | Data Table |  |
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| 45 | [SID24786359] | Inactive | | | Primary cell-based screen for identification of compounds that inhibit transient receptor potential cation channel C4 (TRPC4). [AID2247, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that inhibit transient receptor potential cation channel C4 (TRPC4). | | AID | 2247 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
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| 46 | [SID24786359] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that allosterically potentiate transient receptor potential cation channel C4 (TRPC4) [AID2227, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that allosterically potentiate transient receptor potential cation channel C4 (TRPC4) | | AID | 2227 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
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| 47 | [SID24786359] | Inactive | | | Primary cell-based screen for identification of compounds that activate transient receptor potential cation channel C4 (TRPC4). [AID2237, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that activate transient receptor potential cation channel C4 (TRPC4). | | AID | 2237 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
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| 48 | [SID24786359] | Inactive | | | High throughput screening of inhibitors of transient receptor potential cation channel C6 (TRPC6) [AID2553, Type: screening] | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | High throughput screening of inhibitors of transient receptor potential cation channel C6 (TRPC6) | | AID | 2553 | | BioAssay type | screening | | Target | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] | | PubMed | | | Data Table |  |
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| 49 | [SID24786359] | Inactive | | | High throughput screening of activators of transient receptor potential cation channel C6 (TRPC6) [AID2550, Type: screening] | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | High throughput screening of activators of transient receptor potential cation channel C6 (TRPC6) | | AID | 2550 | | BioAssay type | screening | | Target | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] | | PubMed | | | Data Table |  |
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| 50 | [SID24786359] | Inactive | | | Colorimetric Assay for Inhibitors for NALP1 [AID2071, Type: screening] | NACHT, LRR and PYD domains-containing protein 1 isoform 1 [Homo sapiens] [gi:14719829] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24786359 | | CID | 5663297 | | Outcome | Inactive | | BioAssay | Colorimetric Assay for Inhibitors for NALP1 | | AID | 2071 | | BioAssay type | screening | | Target | NACHT, LRR and PYD domains-containing protein 1 isoform 1 [Homo sapiens] [gi:14719829] | | PubMed | | | Data Table |  |
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