| 1 | [SID103566186] | Active | IC50 | 0.038 | Inhibition of luciferin binding site of Photuris pennsylvanica luciferase by noncompetitive inhibition assay [AID366888, Type: Literature] | Luciferin 4-monooxygenase [gi:41688574] |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 0.038 [uM] | | BioAssay | Inhibition of luciferin binding site of Photuris pennsylvanica luciferase by noncompetitive inhibition assay | | AID | 366888 | | BioAssay type | Literature | | Target | Luciferin 4-monooxygenase [gi:41688574] | | PubMed | 19215089 | | Data Table |  |
|
| 2 | [SID7975271] | Active | Potency | 0.0757 | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) [AID588342, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 0.0757 [uM] | | BioAssay | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) | | AID | 588342 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
|
| 3 | [SID103566186] | Active | IC50 | 0.08 | Inhibition of luciferin binding site of Photinus pyralis luciferase by noncompetitive inhibition assay [AID366887, Type: Literature] | Luciferin 4-monooxygenase [gi:126501] |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 0.08 [uM] | | BioAssay | Inhibition of luciferin binding site of Photinus pyralis luciferase by noncompetitive inhibition assay | | AID | 366887 | | BioAssay type | Literature | | Target | Luciferin 4-monooxygenase [gi:126501] | | PubMed | 19215089 | | Data Table |  |
|
| 4 | [SID103566186] | Active | IC50 | 0.1 | Inhibition of Photinus pyralis luciferase [AID328182, Type: Literature] | |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 0.1 [uM] | | BioAssay | Inhibition of Photinus pyralis luciferase | | AID | 328182 | | BioAssay type | Literature | | Target | | | PubMed | 18363348 | | Data Table |  |
|
| 5 | [SID7975271] | Active | EC50 | 0.122 | Luminescence Biochemical Dose Response HTS to Identify Inhibitors of Luciferase [AID1891, Type: confirmatory] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | EC50 | 0.122 [uM] | | BioAssay | Luminescence Biochemical Dose Response HTS to Identify Inhibitors of Luciferase | | AID | 1891 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 6 | [SID103566186] | Active | IC50 | 0.14 | Inhibition of Photinus pyralis luciferase by Steady-Glo reporter gene assay [AID328185, Type: Literature] | |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 0.14 [uM] | | BioAssay | Inhibition of Photinus pyralis luciferase by Steady-Glo reporter gene assay | | AID | 328185 | | BioAssay type | Literature | | Target | | | PubMed | 18363348 | | Data Table |  |
|
| 7 | [SID7975271] | Active | EC50 | 0.16 | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) [AID2382, Type: confirmatory] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | EC50 | 0.16 [uM] | | BioAssay | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) | | AID | 2382 | | BioAssay type | confirmatory | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
|
| 8 | [SID7975271] | Active | EC50 | 0.16 | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) [AID2382, Type: confirmatory] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | EC50 | 0.16 [uM] | | BioAssay | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) | | AID | 2382 | | BioAssay type | confirmatory | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
|
| 9 | [SID7975271] | Active | EC50 | 0.189 | Luminescence Cell-Based Dose Confirmation HTS to Identify Inhibitors of Platelet Dense Granule Release [AID1889, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | EC50 | 0.189 [uM] | | BioAssay | Luminescence Cell-Based Dose Confirmation HTS to Identify Inhibitors of Platelet Dense Granule Release | | AID | 1889 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 10 | [SID7975271] | Active | Potency | 0.2512 | qHTS Assay for Inhibitors of Firefly Luciferase [AID411, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 0.2512 [uM] | | BioAssay | qHTS Assay for Inhibitors of Firefly Luciferase | | AID | 411 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
|
| 11 | [SID88443004] | Active | IC50 | 0.28494 | Late stage results from the probe development effort to identify inhibitors of kruppel-like factor 5 (KLF5): luminescence-based cell-based dose response assay for inhibitors of KLF5 [AID2750, Type: confirmatory] | Kruppel-like factor 5 [Homo sapiens] [gi:124263658] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 88443004 | | CID | 838877 | | Outcome | Active | | IC50 | 0.28494 [uM] | | BioAssay | Late stage results from the probe development effort to identify inhibitors of kruppel-like factor 5 (KLF5): luminescence-based cell-based dose response assay for inhibitors of KLF5 | | AID | 2750 | | BioAssay type | confirmatory | | Target | Kruppel-like factor 5 [Homo sapiens] [gi:124263658] | | PubMed | | | Data Table |  |
|
| 12 | [SID103566186] | Active | IC50 | 0.3 | Inhibition of Photinus pyralis luciferase by BrightGlo reporter gene assay [AID328186, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 0.3 [uM] | | BioAssay | Inhibition of Photinus pyralis luciferase by BrightGlo reporter gene assay | | AID | 328186 | | BioAssay type | Literature | | Target | | | PubMed | 18363348 | | Data Table |  |
|
| 13 | [SID7975271] | Active | IC50 | 0.3596 | Luminescence-based dose response cell-based high throughput screening assay for inhibitors of kruppel-like factor 5 (KLF5). [AID1973, Type: confirmatory] | Kruppel-like factor 5 [Homo sapiens] [gi:124263658] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | IC50 | 0.3596 [uM] | | BioAssay | Luminescence-based dose response cell-based high throughput screening assay for inhibitors of kruppel-like factor 5 (KLF5). | | AID | 1973 | | BioAssay type | confirmatory | | Target | Kruppel-like factor 5 [Homo sapiens] [gi:124263658] | | PubMed | | | Data Table |  |
|
| 14 | [SID103566186] | Active | IC50 | 0.5 | Inhibition of Photinus pyralis luciferase by Easy lite assay [AID328183, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 0.5 [uM] | | BioAssay | Inhibition of Photinus pyralis luciferase by Easy lite assay | | AID | 328183 | | BioAssay type | Literature | | Target | | | PubMed | 18363348 | | Data Table |  |
|
| 15 | [SID7975271] | Active | IC50 | 0.967 | Dose response confirmation of uHTS chemical inhibitors of both B-cell and T-cell specific antigen receptor-induced NF-kB activation in a 697B cell line using a luminescence assay [AID489034, Type: confirmatory] | |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | IC50 | 0.967 [uM] | | BioAssay | Dose response confirmation of uHTS chemical inhibitors of both B-cell and T-cell specific antigen receptor-induced NF-kB activation in a 697B cell line using a luminescence assay | | AID | 489034 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 16 | [SID7975271] | Active | Potency | 1 | qHTS Assay for Rab9 Promoter Activators [AID485297, Type: confirmatory] | RAB9A gene product [Homo sapiens] [gi:4759012] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 1 [uM] | | BioAssay | qHTS Assay for Rab9 Promoter Activators | | AID | 485297 | | BioAssay type | confirmatory | | Target | RAB9A gene product [Homo sapiens] [gi:4759012] | | PubMed | | | Data Table |  |
|
| 17 | [SID7975271] | Active | IC50 | 1.17 | Dose response confirmation of uHTS of chemical inhibitors of both B-cell and T-cell specific antigen receptor-induced NF-kB activation in a Jurkat cell line using a luminescence assay [AID489004, Type: confirmatory] | |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | IC50 | 1.17 [uM] | | BioAssay | Dose response confirmation of uHTS of chemical inhibitors of both B-cell and T-cell specific antigen receptor-induced NF-kB activation in a Jurkat cell line using a luminescence assay | | AID | 489004 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 18 | [SID7975271] | Active | Potency | 1.4125 | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity [AID2546, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 1.4125 [uM] | | BioAssay | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2546 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 19 | [SID7975271] | Active | Potency | 1.5849 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 20 | [SID7975271] | Active | Potency | 1.5849 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 21 | [SID7975271] | Active | Potency | 1.5849 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 22 | [SID7975271] | Active | Potency | 1.5849 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 23 | [SID7975271] | Active | IC50 | 1.69 | Dose response counterscreen of uHTS chemical inhibitors of both B-cell and T-cell specific antigen receptor-induced NF-kB activation in a HEK-293T cell line using a luminescence assay [AID489020, Type: confirmatory] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | IC50 | 1.69 [uM] | | BioAssay | Dose response counterscreen of uHTS chemical inhibitors of both B-cell and T-cell specific antigen receptor-induced NF-kB activation in a HEK-293T cell line using a luminescence assay | | AID | 489020 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 24 | [SID7975271] | Active | EC50 | 1.691 | Luminescence Cell-Based Dose Confirmation HTS to Identify Compounds Cytotoxic to BJeLR RAS-Dependent Fibroblast [AID1936, Type: confirmatory] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | EC50 | 1.691 [uM] | | BioAssay | Luminescence Cell-Based Dose Confirmation HTS to Identify Compounds Cytotoxic to BJeLR RAS-Dependent Fibroblast | | AID | 1936 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 25 | [SID7975271] | Active | Potency | 2.2387 | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition [AID1379, Type: confirmatory] | luciferase [Photuris pennsylvanica] [gi:1669525] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition | | AID | 1379 | | BioAssay type | confirmatory | | Target | luciferase [Photuris pennsylvanica] [gi:1669525] | | PubMed | | | Data Table |  |
|
| 26 | [SID7975271] | Active | Potency | 2.5119 | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2551 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 27 | [SID103566186] | Active | IC50 | 2.6 | Inhibition of Photinus pyralis luciferase by PK-Light assay [AID328181, Type: Literature] | |   View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 2.6 [uM] | | BioAssay | Inhibition of Photinus pyralis luciferase by PK-Light assay | | AID | 328181 | | BioAssay type | Literature | | Target | | | PubMed | 18363348 | | Data Table |  |
|
| 28 | [SID7975271] | Active | Potency | 3.1623 | qHTS Assay for Anthrax Lethal Toxin Internalization [AID912, Type: confirmatory] | lethal factor [Bacillus anthracis str. A2012] [gi:21392848] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Assay for Anthrax Lethal Toxin Internalization | | AID | 912 | | BioAssay type | confirmatory | | Target | lethal factor [Bacillus anthracis str. A2012] [gi:21392848] | | PubMed | | | Data Table |  |
|
| 29 | [SID7975271] | Active | Potency | 3.1623 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 30 | [SID7975271] | Active | Potency | 3.1623 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 31 | [SID7975271] | Active | Potency | 3.1623 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 32 | [SID7975271] | Active | Potency | 3.1623 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 33 | [SID7975271] | Active | EC50 | 3.272 | Luminescence Cell-Based Dose Response HTS to Identify Compounds Cytotoxic to DRD Non-Viral Oncogenic Fibroblast [AID1934, Type: confirmatory] | |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | EC50 | 3.272 [uM] | | BioAssay | Luminescence Cell-Based Dose Response HTS to Identify Compounds Cytotoxic to DRD Non-Viral Oncogenic Fibroblast | | AID | 1934 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 34 | [SID7975271] | Active | EC50 | 3.638 | Luminescence Cell-Based Dose Response HTS to Identify Compounds Cytotoxic to BJ-TERT RAS-Independent Fibroblast [AID1933, Type: confirmatory] | |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | EC50 | 3.638 [uM] | | BioAssay | Luminescence Cell-Based Dose Response HTS to Identify Compounds Cytotoxic to BJ-TERT RAS-Independent Fibroblast | | AID | 1933 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 35 | [SID7975271] | Active | AC50 | 3.75 | Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Based System Using Plate Reader - 2134-01_Inhibitor_Dose_CherryPick_Activity [AID624132, Type: confirmatory] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | AC50 | 3.75 [uM] | | BioAssay | Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Based System Using Plate Reader - 2134-01_Inhibitor_Dose_CherryPick_Activity | | AID | 624132 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 36 | [SID7975271] | Active | AC50 | 5.26 | Shn3: Cytotox assay Measured in Cell-Based System Using Plate Reader - 2134-03_Inhibitor_Dose_CherryPick_Activity [AID624134, Type: confirmatory] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | AC50 | 5.26 [uM] | | BioAssay | Shn3: Cytotox assay Measured in Cell-Based System Using Plate Reader - 2134-03_Inhibitor_Dose_CherryPick_Activity | | AID | 624134 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 37 | [SID7975271] | Active | Potency | 7.0795 | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen [AID588856, Type: confirmatory] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 7.0795 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen | | AID | 588856 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 38 | [SID7975271] | Active | IC50 | 9.085 | Luminescence-based counterscreen assay for KLF5 inhibitors: dose response cell-based high throughput screening assay to identify cytotoxic compounds using the IEC-6 intestinal epithelial cell line. [AID1975, Type: confirmatory] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | IC50 | 9.085 [uM] | | BioAssay | Luminescence-based counterscreen assay for KLF5 inhibitors: dose response cell-based high throughput screening assay to identify cytotoxic compounds using the IEC-6 intestinal epithelial cell line. | | AID | 1975 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 39 | [SID7975271] | Active | Potency | 10 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line [AID686970, Type: confirmatory] | IDH1 [Homo sapiens] [gi:49168486] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line | | AID | 686970 | | BioAssay type | confirmatory | | Target | IDH1 [Homo sapiens] [gi:49168486] | | PubMed | | | Data Table |  |
|
| 40 | [SID7975271] | Active | Potency | 10.3225 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 10.3225 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 41 | [SID103566186] | Active | IC50 | 11.3 | Inhibition of luciferin binding site of Photuris pennsylvanica luciferase by noncompetitive KinaseGlo luminescent assay [AID366886, Type: Literature] | Luciferin 4-monooxygenase [gi:41688574] |   View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 103566186 | | CID | 838877 | | Outcome | Active | | IC50 | 11.3 [uM] | | BioAssay | Inhibition of luciferin binding site of Photuris pennsylvanica luciferase by noncompetitive KinaseGlo luminescent assay | | AID | 366886 | | BioAssay type | Literature | | Target | Luciferin 4-monooxygenase [gi:41688574] | | PubMed | 19215089 | | Data Table |  |
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| 42 | [SID7975271] | Active | Potency | 11.5821 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 11.5821 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 43 | [SID7975271] | Active | Potency | 12.5893 | 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. | 43 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 12.5893 [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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| 44 | [SID7975271] | Active | Potency | 14.1254 | qHTS Assay for Inhibitors of Leishmania Mexicana Pyruvate Kinase (LmPK) [AID1721, Type: confirmatory] | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 14.1254 [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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| 45 | [SID7975271] | Active | Potency | 25.1189 | qHTS Assay for Activators of ClpP [AID651965, Type: confirmatory] | ClpP [Bacillus subtilis] [gi:2668494] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for Activators of ClpP | | AID | 651965 | | BioAssay type | confirmatory | | Target | ClpP [Bacillus subtilis] [gi:2668494] | | PubMed | | | Data Table |  |
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| 46 | [SID7975271] | Active | AC50 | 32.66 | Shn3: Dual-Go Shn3RL cells Measured in Cell-Based System Using Plate Reader - 2134-02_Inhibitor_Dose_CherryPick_Activity [AID624133, Type: confirmatory] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | AC50 | 32.66 [uM] | | BioAssay | Shn3: Dual-Go Shn3RL cells Measured in Cell-Based System Using Plate Reader - 2134-02_Inhibitor_Dose_CherryPick_Activity | | AID | 624133 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID7975271] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
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| 48 | [SID7975271] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of the HIV-1 protein Vpr [AID651644, Type: confirmatory] | Vpr [Human immunodeficiency virus 1] [gi:28872817] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of the HIV-1 protein Vpr | | AID | 651644 | | BioAssay type | confirmatory | | Target | Vpr [Human immunodeficiency virus 1] [gi:28872817] | | PubMed | | | Data Table |  |
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| 49 | [SID7975271] | Active | Potency | 52.6732 | Confirmation qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID2701, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | Potency | 52.6732 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 2701 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
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| 50 | [SID7975271] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of COUP-TFII (NR2F2) [AID686940, Type: screening] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 7975271 | | CID | 838877 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of COUP-TFII (NR2F2) | | AID | 686940 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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