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TargetCyclin-dependent kinase 7
LigandBDBM32348
Substrate/Competitorn/a
Meas. Tech.CDK7 counterscreen of confirmed PKD inhibitors-57K library addition
IC50 8222.176091±n/a nM
Citation PubChem, PC CDK7 counterscreen of confirmed PKD inhibitors-57K library addition PubChem Bioassay(2008)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Cyclin-dependent kinase 7
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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  Blast E-value cutoff:
BDBM32348
n/a
NameBDBM32348
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
TypeSmall organic molecule
Emp. Form.C13H13N5O2
Mol. Mass.271.2746
SMILESCC1Cc2ccccc2N1c1ncnc(N)c1[N+]([O-])=O
Structure
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