Reaction Details |
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Target | 1-acyl-sn-glycerol-3-phosphate acyltransferase beta |
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Ligand | BDBM50141254 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_100169 |
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IC50 | 27±n/a nM |
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Citation | Gong, B; Hong, F; Kohm, C; Bonham, L; Klein, 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 |
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More Info.: | Get all data from this article, Assay Method |
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1-acyl-sn-glycerol-3-phosphate acyltransferase beta |
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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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BDBM50141254 |
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n/a |
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Name | BDBM50141254 |
Synonyms: | CHEMBL422579 | N-[4-Chloro-3-(5-chloro-benzooxazol-2-yl)-phenyl]-2-cyano-acetamide |
Type | Small organic molecule |
Emp. Form. | C16H9Cl2N3O2 |
Mol. Mass. | 346.168 |
SMILES | Clc1ccc2oc(nc2c1)-c1cc(NC(=O)CC#N)ccc1Cl |
Structure |
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