Reaction Details |
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Target | 1-acyl-sn-glycerol-3-phosphate acyltransferase beta |
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Ligand | BDBM50141255 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_100169 |
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IC50 | 15±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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BDBM50141255 |
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n/a |
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Name | BDBM50141255 |
Synonyms: | CHEMBL35508 | [3-(5-Chloro-benzothiazol-2-yl)-4-methyl-phenyl]-carbamic acid prop-2-ynyl ester |
Type | Small organic molecule |
Emp. Form. | C18H13ClN2O2S |
Mol. Mass. | 356.826 |
SMILES | Cc1ccc(NC(=O)OCC#C)cc1-c1nc2cc(Cl)ccc2s1 |
Structure |
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