| 1 | [SID24814942] | Active | Potency | 9.5283 | 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. | 1 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | Potency | 9.5283 [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 |  |
|
| 2 | [SID24814942] | Active | | | Counter screen for compounds that protect hERG from block by proarrhythmic agents [AID1839, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Counter screen for compounds that protect hERG from block by proarrhythmic agents | | AID | 1839 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 3 | [SID24814942] | Active | | | Counter screen for compounds that protect hERG from block by proarrhythmic agents [AID1839, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Counter screen for compounds that protect hERG from block by proarrhythmic agents | | AID | 1839 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 4 | [SID24814942] | Active | | | Counter screen for compounds that protect hERG from block by proarrhythmic agents [AID1839, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Counter screen for compounds that protect hERG from block by proarrhythmic agents | | AID | 1839 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 5 | [SID24814942] | Active | | | Counter screen for compounds that protect hERG from block by proarrhythmic agents [AID1839, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Counter screen for compounds that protect hERG from block by proarrhythmic agents | | AID | 1839 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 6 | [SID24814942] | Active | | | Counter screen for compounds that protect hERG from block by proarrhythmic agents [AID1839, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Counter screen for compounds that protect hERG from block by proarrhythmic agents | | AID | 1839 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 7 | [SID24814942] | Active | | | Specificity screen against KCNQ1 for compounds that potentiate KCNQ2 potassium channels [AID2283, Type: screening] | KCNQ1 gene product [Homo sapiens] [gi:32479527] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Specificity screen against KCNQ1 for compounds that potentiate KCNQ2 potassium channels | | AID | 2283 | | BioAssay type | screening | | Target | KCNQ1 gene product [Homo sapiens] [gi:32479527] | | PubMed | | | Data Table |  |
|
| 8 | [SID24814942] | Active | | | Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels [AID2239, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels | | AID | 2239 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 9 | [SID24814942] | Active | | | Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels [AID2239, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that potentiate KCNQ2 potassium channels | | AID | 2239 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 10 | [SID24814942] | Active | | | Confirmatory screen for compounds that potentiate KCNQ2 potassium channels [AID2287, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Confirmatory screen for compounds that potentiate KCNQ2 potassium channels | | AID | 2287 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 11 | [SID24814942] | Active | | | Confirmatory screen for compounds that potentiate KCNQ2 potassium channels [AID2287, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Confirmatory screen for compounds that potentiate KCNQ2 potassium channels | | AID | 2287 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 12 | [SID24814942] | Active | | | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) [AID488975, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) | | AID | 488975 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 13 | [SID24814942] | Active | | | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) [AID488975, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) | | AID | 488975 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 14 | [SID24814942] | Active | | | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay [AID463195, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay | | AID | 463195 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
|
| 15 | [SID24814942] | Active | | | Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels [AID2648, Type: screening] | KCNQ1 gene product [Homo sapiens] [gi:32479527] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that potentiate/activate KCNQ1 potassium channels | | AID | 2648 | | BioAssay type | screening | | Target | KCNQ1 gene product [Homo sapiens] [gi:32479527] | | PubMed | | | Data Table |  |
|
| 16 | [SID24814942] | Active | | | KCNQ2 Counter screen for compounds that protect hERG from block by proarrhythmic agents [AID1942, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | KCNQ2 Counter screen for compounds that protect hERG from block by proarrhythmic agents | | AID | 1942 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 17 | [SID24814942] | Active | | | KCNQ2 Counter screen for compounds that protect hERG from block by proarrhythmic agents [AID1942, Type: screening] | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | KCNQ2 Counter screen for compounds that protect hERG from block by proarrhythmic agents | | AID | 1942 | | BioAssay type | screening | | Target | Kcnq2 gene product [Rattus norvegicus] [gi:18959272] | | PubMed | | | Data Table |  |
|
| 18 | [SID24814942] | Active | | | uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent assay [AID463212, Type: screening] | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent assay | | AID | 463212 | | BioAssay type | screening | | Target | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] | | PubMed | | | Data Table |  |
|
| 19 | [SID24814942] | Active | | | Single concentration confirmation of small molecule inhibitors of tim23-1 yeast via a luminescent assay [AID463218, Type: screening] | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Active | | BioAssay | Single concentration confirmation of small molecule inhibitors of tim23-1 yeast via a luminescent assay | | AID | 463218 | | BioAssay type | screening | | Target | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] | | PubMed | | | Data Table |  |
|
| 20 | [SID24814942] | Inactive | Potency | 2.0787 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | Potency | 2.0787 [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 |  |
|
| 21 | [SID24814942] | Inactive | Potency | 7.0795 | qHTS Assay for Identification of Novel General Anesthetics [AID485281, Type: confirmatory] | Chain A, Horse Spleen Apoferritin [gi:254220970] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for Identification of Novel General Anesthetics | | AID | 485281 | | BioAssay type | confirmatory | | Target | Chain A, Horse Spleen Apoferritin [gi:254220970] | | PubMed | | | Data Table |  |
|
| 22 | [SID24814942] | Inactive | Potency | 13.1154 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | Potency | 13.1154 [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 |  |
|
| 23 | [SID24814942] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels [AID2642, Type: screening] | KCNQ1 gene product [Homo sapiens] [gi:32479527] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that inhibit KCNQ1 potassium channels | | AID | 2642 | | BioAssay type | screening | | Target | KCNQ1 gene product [Homo sapiens] [gi:32479527] | | PubMed | | | Data Table |  |
|
| 24 | [SID24814942] | Inactive | | | HTS to identify inhibitors of zVAD Induced Cell Death in L929 Cells. [AID1377, Type: screening] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | HTS to identify inhibitors of zVAD Induced Cell Death in L929 Cells. | | AID | 1377 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 25 | [SID24814942] | Inactive | | | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. [AID1381, Type: screening] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. | | AID | 1381 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 26 | [SID24814942] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 27 | [SID24814942] | Inactive | EC50 | | Screen for small molecule probes relevant to Friedreich's ataxia, Single Dose and Dose Response [AID1465, Type: confirmatory] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | 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 |  |
|
| 28 | [SID24814942] | Inactive | | | Counterscreen for inhibitors of Janus kinase 2 mutant JAK2V617F: Cell-based high throughput assay to identify inhibitors of parental Ba/F3 cell viability. [AID1486, Type: screening] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Counterscreen for inhibitors of Janus kinase 2 mutant JAK2V617F: Cell-based high throughput assay to identify inhibitors of parental Ba/F3 cell viability. | | AID | 1486 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 29 | [SID24814942] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents [AID1511, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | | AID | 1511 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 30 | [SID24814942] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents [AID1511, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | | AID | 1511 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 31 | [SID24814942] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents [AID1511, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | | AID | 1511 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 32 | [SID24814942] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents [AID1511, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | | AID | 1511 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 33 | [SID24814942] | Inactive | | | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents [AID1511, Type: screening] | putative potassium channel subunit [Homo sapiens] [gi:487738] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay for identification of compounds that protect hERG from block by proarrhythmic agents | | AID | 1511 | | BioAssay type | screening | | Target | putative potassium channel subunit [Homo sapiens] [gi:487738] | | PubMed | | | Data Table |  |
|
| 34 | [SID24814942] | Inactive | Potency | | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding [AID2675, Type: confirmatory] | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding | | AID | 2675 | | BioAssay type | confirmatory | | Target | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] | | PubMed | | | Data Table |  |
|
| 35 | [SID24814942] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. [AID2057, Type: screening] | Myeloid cell leukemia sequence 1 (BCL2-related) [Homo sapiens] [gi:78070770] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. | | AID | 2057 | | BioAssay type | screening | | Target | Myeloid cell leukemia sequence 1 (BCL2-related) [Homo sapiens] [gi:78070770] | | PubMed | | | Data Table |  |
|
| 36 | [SID24814942] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. [AID2057, Type: screening] | Myeloid cell leukemia sequence 1 (BCL2-related) [Homo sapiens] [gi:78070770] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. | | AID | 2057 | | BioAssay type | screening | | Target | Myeloid cell leukemia sequence 1 (BCL2-related) [Homo sapiens] [gi:78070770] | | PubMed | | | Data Table |  |
|
| 37 | [SID24814942] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. [AID2057, Type: screening] | Myeloid cell leukemia sequence 1 (BCL2-related) [Homo sapiens] [gi:78070770] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. | | AID | 2057 | | BioAssay type | screening | | Target | Myeloid cell leukemia sequence 1 (BCL2-related) [Homo sapiens] [gi:78070770] | | PubMed | | | Data Table |  |
|
| 38 | [SID24814942] | Inactive | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 39 | [SID24814942] | Inactive | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 40 | [SID24814942] | Inactive | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 41 | [SID24814942] | Inactive | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 42 | [SID24814942] | Inactive | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 43 | [SID24814942] | Inactive | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 44 | [SID24814942] | Inactive | | | uHTS for identification of Inhibitors of Mdm2/MdmX interaction in luminescent format. [AID485346, Type: screening] | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS for identification of Inhibitors of Mdm2/MdmX interaction in luminescent format. | | AID | 485346 | | BioAssay type | screening | | Target | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] | | PubMed | | | Data Table |  |
|
| 45 | [SID24814942] | Inactive | | | uHTS for identification of Inhibitors of Mdm2/MdmX interaction in luminescent format. [AID485346, Type: screening] | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | uHTS for identification of Inhibitors of Mdm2/MdmX interaction in luminescent format. | | AID | 485346 | | BioAssay type | screening | | Target | protein Mdm4 isoform 1 [Homo sapiens] [gi:88702791] | | PubMed | | | Data Table |  |
|
| 46 | [SID24814942] | Inactive | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
|
| 47 | [SID24814942] | Inactive | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
|
| 48 | [SID24814942] | Inactive | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
|
| 49 | [SID24814942] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1441, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1441 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 50 | [SID24814942] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. [AID1441, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24814942 | | CID | 16194533 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | | AID | 1441 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|