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Target1-acyl-sn-glycerol-3-phosphate acyltransferase beta
LigandBDBM50141254
Substrate/Competitorn/a
Meas. Tech.ChEBML_100169
IC50 27±n/a nM
Citation Gong, BHong, FKohm, CBonham, LKlein, P Synthesis and SAR of 2-arylbenzoxazoles, benzothiazoles and benzimidazoles as inhibitors of lysophosphatidic acid acyltransferase-beta. Bioorg Med Chem Lett14:1455-9 (2004) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
1-acyl-sn-glycerol-3-phosphate acyltransferase beta
Name:1-acyl-sn-glycerol-3-phosphate acyltransferase beta
Synonyms:1-acylglycerol-3-phosphate O-acyltransferase beta | AGPAT2 | PLCB_HUMAN
Type:PROTEIN
Mol. Mass.:30924.09
Organism:Homo sapiens (Human)
Description:ChEMBL_321473
Residue:278
Sequence:
MELWPCLAAALLLLLLLVQLSRAAEFYAKVALYCALCFTVSAVASLVCLLRHGGRTVENM
SIIGWFVRSFKYFYGLRFEVRDPRRLQEARPCVIVSNHQSILDMMGLMEVLPERCVQIAK
RELLFLGPVGLIMYLGGVFFINRQRSSTAMTVMADLGERMVRENLKVWIYPEGTRNDNGD
LLPFKKGAFYLAVQAQVPIVPVVYSSFSSFYNTKKKFFTSGTVTVQVLEAIPTSGLTAAD
VPALVDTCHRAMRTTFLHISKTPQENGATAGSGVQPAQ
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  Blast E-value cutoff:
BDBM50141254
n/a
NameBDBM50141254
Synonyms:CHEMBL422579 | N-[4-Chloro-3-(5-chloro-benzooxazol-2-yl)-phenyl]-2-cyano-acetamide
TypeSmall organic molecule
Emp. Form.C16H9Cl2N3O2
Mol. Mass.346.168
SMILESClc1ccc2oc(nc2c1)-c1cc(NC(=O)CC#N)ccc1Cl
Structure
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