| 1 | [SID24823303] | Active | IC50 | 7.123 | Dose Response confirmation of uHTS hits for Scp-1 phosphatase using a colorimetric assay [AID540297, Type: confirmatory] | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | IC50 | 7.123 [uM] | | BioAssay | Dose Response confirmation of uHTS hits for Scp-1 phosphatase using a colorimetric assay | | AID | 540297 | | BioAssay type | confirmatory | | Target | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] | | PubMed | | | Data Table |  |
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| 2 | [SID24823303] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of Leishmania Mexicana Pyruvate Kinase (LmPK) [AID1721, Type: confirmatory] | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of Leishmania Mexicana Pyruvate Kinase (LmPK) | | AID | 1721 | | BioAssay type | confirmatory | | Target | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] | | PubMed | | | Data Table |  |
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| 3 | [SID24823303] | Active | IC50 | 24.6 | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. [AID1986, Type: confirmatory] | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | IC50 | 24.6 [uM] | | BioAssay | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. | | AID | 1986 | | BioAssay type | confirmatory | | Target | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | | PubMed | | | Data Table |  |
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| 4 | [SID24823303] | Active | IC50 | 47.94 | Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition [AID588689, Type: confirmatory] | Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocyste [gi:219689243] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | IC50 | 47.94 [uM] | | BioAssay | Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition | | AID | 588689 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocyste [gi:219689243] | | PubMed | | | Data Table |  |
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| 5 | [SID24823303] | Active | Potency | 50.1187 | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain [AID504339, Type: confirmatory] | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | Potency | 50.1187 [uM] | | BioAssay | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain | | AID | 504339 | | BioAssay type | confirmatory | | Target | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] | | PubMed | | | Data Table |  |
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| 6 | [SID24823303] | Active | Potency | 56.2341 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | Potency | 56.2341 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
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| 7 | [SID24823303] | Active | | | Single concentration confirmation of uHTS hits for Scp-1 phosphatase using a colorimetric assay [AID540281, Type: screening] | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS hits for Scp-1 phosphatase using a colorimetric assay | | AID | 540281 | | BioAssay type | screening | | Target | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] | | PubMed | | | Data Table |  |
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| 8 | [SID24823303] | Active | | | uHTS Colorimetric assay for identification of inhibitors of Scp-1 [AID493091, Type: screening] | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | uHTS Colorimetric assay for identification of inhibitors of Scp-1 | | AID | 493091 | | BioAssay type | screening | | Target | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] | | PubMed | | | Data Table |  |
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| 9 | [SID24823303] | Active | | | Fluorescence-based biochemical primary high throughput screening assay to identify molecules that bind r(CAG) RNA repeats [AID651821, Type: screening] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify molecules that bind r(CAG) RNA repeats | | AID | 651821 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 10 | [SID24823303] | Active | | | Fluorescence-based biochemical high throughput confirmation assay to identify molecules that bind r(CAG) RNA repeats [AID652065, Type: screening] | |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput confirmation assay to identify molecules that bind r(CAG) RNA repeats | | AID | 652065 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 11 | [SID24823303] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) [AID463082, Type: screening] | PLA2G7 gene product [Homo sapiens] [gi:270133071] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | | AID | 463082 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 12 | [SID24823303] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) [AID463082, Type: screening] | PLA2G7 gene product [Homo sapiens] [gi:270133071] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the plasma platelet activating factor acetylhydrolase (pPAFAH) | | AID | 463082 | | BioAssay type | screening | | Target | PLA2G7 gene product [Homo sapiens] [gi:270133071] | | PubMed | | | Data Table |  |
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| 13 | [SID24823303] | Active | | | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Absorbance-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) full deck assay to identify assay artifacts [AID588335, Type: screening] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Absorbance-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) full deck assay to identify assay artifacts | | AID | 588335 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 14 | [SID24823303] | Active | | | Counterscreen for molecules that bind rCAG RNA repeats: fluorescent based biochemical counterscreen assay for inhibitors of the DNA-based (5'CAG/3'GTC) TO-PRO-1 dye complex [AID652068, Type: screening] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Active | | BioAssay | Counterscreen for molecules that bind rCAG RNA repeats: fluorescent based biochemical counterscreen assay for inhibitors of the DNA-based (5'CAG/3'GTC) TO-PRO-1 dye complex | | AID | 652068 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 15 | [SID24823303] | 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. | 15 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | 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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| 16 | [SID24823303] | 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. | 16 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | 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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| 17 | [SID24823303] | Inactive | Potency | 12.5893 | qHTS Assay for Activators of Leishmania Mexicana Pyruvate Kinase (LmPK) [AID1722, Type: confirmatory] | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Activators of Leishmania Mexicana Pyruvate Kinase (LmPK) | | AID | 1722 | | BioAssay type | confirmatory | | Target | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] | | PubMed | | | Data Table |  |
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| 18 | [SID24823303] | Inactive | Potency | 13.1154 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | Potency | 13.1154 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | | AID | 504832 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 19 | [SID24823303] | Inactive | Potency | | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | 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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| 20 | [SID24823303] | Inactive | Potency | | qHTS for Inhibitors of binding or entry into cells for Lassa Virus [AID540256, Type: confirmatory] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of binding or entry into cells for Lassa Virus | | AID | 540256 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 21 | [SID24823303] | Inactive | | | Small Molecules that selectively kill Giardia lamblia: qHTS [AID540267, Type: screening] | |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Small Molecules that selectively kill Giardia lamblia: qHTS | | AID | 540267 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 22 | [SID24823303] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify activators of the GAA850 frataxin (FXN) promoter [AID540364, Type: screening] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify activators of the GAA850 frataxin (FXN) promoter | | AID | 540364 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 23 | [SID24823303] | Inactive | | | MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint_HTS_Activity [AID588334, Type: screening] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint_HTS_Activity | | AID | 588334 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 24 | [SID24823303] | Inactive | Potency | | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line [AID686971, Type: confirmatory] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line | | AID | 686971 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 25 | [SID24823303] | Inactive | | | VEID(2) R110 Enzymatic Primary HTS to identify Inhibitors of Caspase 6 Measured in Biochemical System Using Plate Reader - 7052-01_Inhibitor_SinglePoint_HTS_Activity_Set2 [AID686996, Type: screening] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | VEID(2) R110 Enzymatic Primary HTS to identify Inhibitors of Caspase 6 Measured in Biochemical System Using Plate Reader - 7052-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | | AID | 686996 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 26 | [SID24823303] | Inactive | | | Counter Screen for Glucose-6-Phosphate Dehydrogenase-based Primary Assay [AID1020, Type: screening] | glucose-6-phosphate dehydrogenase [Leuconostoc mesenteroides] [gi:149631] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Counter Screen for Glucose-6-Phosphate Dehydrogenase-based Primary Assay | | AID | 1020 | | BioAssay type | screening | | Target | glucose-6-phosphate dehydrogenase [Leuconostoc mesenteroides] [gi:149631] | | PubMed | | | Data Table |  |
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| 27 | [SID24823303] | Inactive | | | Screen for Chemicals that Inhibit the RAM Network [AID868, Type: screening] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Screen for Chemicals that Inhibit the RAM Network | | AID | 868 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 28 | [SID24823303] | Inactive | | | NIH Compound Library Profiling: Compound and DTT Dependent Redox Cycling H2O2 Generation. [AID878, Type: screening] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | NIH Compound Library Profiling: Compound and DTT Dependent Redox Cycling H2O2 Generation. | | AID | 878 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 29 | [SID24823303] | Inactive | | | Counter Screen for Luciferase-based Primary Inhibition Assays [AID1006, Type: screening] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Counter Screen for Luciferase-based Primary Inhibition Assays | | AID | 1006 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 30 | [SID24823303] | Inactive | | | Counter Screen for Luciferase-based Primary Stimulation Assays [AID1027, Type: screening] | |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Counter Screen for Luciferase-based Primary Stimulation Assays | | AID | 1027 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 31 | [SID24823303] | Inactive | | | Leishmania major promastigote HTS [AID1063, Type: screening] | |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Leishmania major promastigote HTS | | AID | 1063 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 32 | [SID24823303] | Inactive | | | Anti-Viral Drugs Against Arbovirus Infections, a Primary Screen [AID1251, Type: screening] | |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Anti-Viral Drugs Against Arbovirus Infections, a Primary Screen | | AID | 1251 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 33 | [SID24823303] | Inactive | | | Chemical Genetic Screen to Identify Inhibitors of Mitochondrial Fusion - Primary Screen [AID1362, Type: screening] | |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Chemical Genetic Screen to Identify Inhibitors of Mitochondrial Fusion - Primary Screen | | AID | 1362 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 34 | [SID24823303] | Inactive | | | HTS to identify inhibitors of zVAD Induced Cell Death in L929 Cells. [AID1377, Type: screening] | |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | HTS to identify inhibitors of zVAD Induced Cell Death in L929 Cells. | | AID | 1377 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 35 | [SID24823303] | Inactive | | | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. [AID1381, Type: screening] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. | | AID | 1381 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 36 | [SID24823303] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 37 | [SID24823303] | Inactive | EC50 | | Screen for small molecule probes relevant to Friedreich's ataxia, Single Dose and Dose Response [AID1465, Type: confirmatory] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | EC50 | [uM] | | BioAssay | Screen for small molecule probes relevant to Friedreich's ataxia, Single Dose and Dose Response | | AID | 1465 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 38 | [SID24823303] | Inactive | | | HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies [AID588358, Type: screening] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies | | AID | 588358 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 39 | [SID24823303] | Inactive | | | Cholera Quorum: HTS for inducers of light production in the absence ofautoinducers using BH1578 (luxS deficient, cqsA deficient) Measured in Microorganism System Using Plate Reader - 2132-01_Agonist_SinglePoint_HTS_Activity [AID588436, Type: screening] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Cholera Quorum: HTS for inducers of light production in the absence ofautoinducers using BH1578 (luxS deficient, cqsA deficient) Measured in Microorganism System Using Plate Reader - 2132-01_Agonist_SinglePoint_HTS_Activity | | AID | 588436 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 40 | [SID24823303] | Inactive | | | uHTS identification of small molecule modulators of myocardial damage [AID588492, Type: screening] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule modulators of myocardial damage | | AID | 588492 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 41 | [SID24823303] | Inactive | | | Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Based System Using Plate Reader - 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2 [AID588674, Type: screening] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Based System Using Plate Reader - 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | | AID | 588674 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 42 | [SID24823303] | Inactive | | | Luciferase Reporter Cell Based HTS to identify inhibitors of N-linked Glycosylation Measured in Cell-Based System Using Plate Reader - 2146-01_Inhibitor_SinglePoint_HTS_Activity_Set2 [AID588692, Type: screening] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Luciferase Reporter Cell Based HTS to identify inhibitors of N-linked Glycosylation Measured in Cell-Based System Using Plate Reader - 2146-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | | AID | 588692 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 43 | [SID24823303] | Inactive | IC50 | | A Cell-Based Confirmatory Screen for Compounds that Inhibit VEEV, TC-83 [AID588727, Type: confirmatory] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A Cell-Based Confirmatory Screen for Compounds that Inhibit VEEV, TC-83 | | AID | 588727 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 44 | [SID24823303] | Inactive | CC50 | | Vero Cytoxicity Assay: A Cell Based Secondary Assay to Explore Cytotoxicity of Compounds that Inhibit Flavivirus Genomic Capping Enzyme [AID588742, Type: confirmatory] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | CC50 | [uM] | | BioAssay | Vero Cytoxicity Assay: A Cell Based Secondary Assay to Explore Cytotoxicity of Compounds that Inhibit Flavivirus Genomic Capping Enzyme | | AID | 588742 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 45 | [SID24823303] | Inactive | Potency | | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen [AID588856, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen | | AID | 588856 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 46 | [SID24823303] | Inactive | | | uHTS determination of small molecule cytotoxicity in a fluorescence assay to identify cystic fibrosis induced NFkb Inhibitors [AID602141, Type: screening] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | uHTS determination of small molecule cytotoxicity in a fluorescence assay to identify cystic fibrosis induced NFkb Inhibitors | | AID | 602141 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID24823303] | Inactive | | | Full deck counterscreen for positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective activators and assay artifacts using the parental CHOK1 cell line [AID602247, Type: screening] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Full deck counterscreen for positive allosteric modulators (PAMs) of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective activators and assay artifacts using the parental CHOK1 cell line | | AID | 602247 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 48 | [SID24823303] | Inactive | | | Full deck counterscreen for agonists of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective activators and assay artifacts using the parental CHOK1 cell line [AID602248, Type: screening] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Full deck counterscreen for agonists of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective activators and assay artifacts using the parental CHOK1 cell line | | AID | 602248 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID24823303] | Inactive | | | Full deck counterscreen for antagonists of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective inhibitors and assay artifacts using the parental CHOK1 cell line [AID602250, Type: screening] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | Full deck counterscreen for antagonists of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective inhibitors and assay artifacts using the parental CHOK1 cell line | | AID | 602250 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID24823303] | Inactive | | | uHTS luminescent assay for identification of compounds that enhance the survival of human induced pluripotent stem cells when cultured as single cells [AID602274, Type: screening] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24823303 | | CID | 46499303 | | Outcome | Inactive | | BioAssay | uHTS luminescent assay for identification of compounds that enhance the survival of human induced pluripotent stem cells when cultured as single cells | | AID | 602274 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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