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Target[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
LigandBDBM50378657
Substrate/Competitorn/a
Meas. Tech.ChEMBL_608417 (CHEMBL1064446)
IC50>10000±n/a nM
Citation Brasca, MGAlbanese, CAlzani, RAmici, RAvanzi, NBallinari, DBischoff, JBorghi, DCasale, ECroci, VFiorentini, FIsacchi, AMercurio, CNesi, MOrsini, PPastori, WPesenti, EPevarello, PRoussel, PVarasi, MVolpi, DVulpetti, ACiomei, M Optimization of 6,6-dimethyl pyrrolo[3,4-c]pyrazoles: Identification of PHA-793887, a potent CDK inhibitor suitable for intravenous dosing. Bioorg Med Chem18:1844-53 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
Name:[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
Synonyms:PDHK1 | PDK1 | PDK1_HUMAN | Pyruvate dehydrogenase kinase | Pyruvate dehydrogenase kinase 1 (PDK1) | Pyruvate dehydrogenase kinase isoform 1
Type:Protein
Mol. Mass.:49255.23
Organism:Homo sapiens (Human)
Description:Q15118
Residue:436
Sequence:
MRLARLLRGAALAGPGPGLRAAGFSRSFSSDSGSSPASERGVPGQVDFYARFSPSPLSMK
QFLDFGSVNACEKTSFMFLRQELPVRLANIMKEISLLPDNLLRTPSVQLVQSWYIQSLQE
LLDFKDKSAEDAKAIYDFTDTVIRIRNRHNDVIPTMAQGVIEYKESFGVDPVTSQNVQYF
LDRFYMSRISIRMLLNQHSLLFGGKGKGSPSHRKHIGSINPNCNVLEVIKDGYENARRLC
DLYYINSPELELEELNAKSPGQPIQVVYVPSHLYHMVFELFKNAMRATMEHHANRGVYPP
IQVHVTLGNEDLTVKMSDRGGGVPLRKIDRLFNYMYSTAPRPRVETSRAVPLAGFGYGLP
ISRLYAQYFQGDLKLYSLEGYGTDAVIYIKALSTDSIERLPVYNKAAWKHYNTNHEADDW
CVPSREPKDMTTFRSA
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  Blast E-value cutoff:
BDBM50378657
n/a
NameBDBM50378657
Synonyms:CHEMBL1230607
TypeSmall organic molecule
Emp. Form.C19H31N5O2
Mol. Mass.361.4817
SMILESCC(C)CC(=O)Nc1[nH]nc2c1CN(C(=O)C1CCN(C)CC1)C2(C)C
Structure
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