Reaction Details |
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Target | Cyclin-dependent kinase 7 |
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Ligand | BDBM32348 |
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Substrate/Competitor | n/a |
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Meas. Tech. | CDK7 counterscreen of confirmed PKD inhibitors-57K library addition |
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IC50 | 8222.176091±n/a nM |
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Citation | PubChem, PC CDK7 counterscreen of confirmed PKD inhibitors-57K library addition PubChem Bioassay(2008)[AID] |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Cyclin-dependent kinase 7 |
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Name: | Cyclin-dependent kinase 7 |
Synonyms: | 39 kDa protein kinase | CAK | CAK1 | CDK-activating kinase | CDK-activating kinase 1 (CAK) | CDK7 | CDK7_HUMAN | CDKN7 | Cell division protein kinase 7 | Cyclin-Dependent Kinase 7 (CDK7) | Cyclin-dependent kinase 7 (CDK7/cyclin H) | MO15 | P39 Mo15 | STK1 | TFIIH basal transcription factor complex kinase subunit |
Type: | Enzyme Subunit |
Mol. Mass.: | 39047.01 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 346 |
Sequence: | MALDVKSRAKRYEKLDFLGEGQFATVYKARDKNTNQIVAIKKIKLGHRSEAKDGINRTAL
REIKLLQELSHPNIIGLLDAFGHKSNISLVFDFMETDLEVIIKDNSLVLTPSHIKAYMLM
TLQGLEYLHQHWILHRDLKPNNLLLDENGVLKLADFGLAKSFGSPNRAYTHQVVTRWYRA
PELLFGARMYGVGVDMWAVGCILAELLLRVPFLPGDSDLDQLTRIFETLGTPTEEQWPDM
CSLPDYVTFKSFPGIPLHHIFSAAGDDLLDLIQGLFLFNPCARITATQALKMKYFSNRPG
PTPGCQLPRPNCPVETLKEQSNPALAIKRKRTEALEQGGLPKKLIF
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BDBM32348 |
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n/a |
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Name | BDBM32348 |
Synonyms: | 6-(2-methyl-2,3-dihydro-1H-indol-1-yl)-5-nitro-4-pyrimidinamine | 6-(2-methyl-2,3-dihydroindol-1-yl)-5-nitro-4-pyrimidinamine | 6-(2-methyl-2,3-dihydroindol-1-yl)-5-nitro-pyrimidin-4-amine | 6-(2-methyl-2,3-dihydroindol-1-yl)-5-nitropyrimidin-4-amine | MLS000665974 | SMR000294670 | [6-(2-methylindolin-1-yl)-5-nitro-pyrimidin-4-yl]amine | cid_2958734 |
Type | Small organic molecule |
Emp. Form. | C13H13N5O2 |
Mol. Mass. | 271.2746 |
SMILES | CC1Cc2ccccc2N1c1ncnc(N)c1[N+]([O-])=O |
Structure |
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