Reaction Details |
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Target | Liver carboxylesterase 1 |
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Ligand | BDBM50073987 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_305902 (CHEMBL832566) |
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IC50 | 5±n/a nM |
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Citation | Leung, D; Du, W; Hardouin, C; Cheng, H; Hwang, I; Cravatt, BF; Boger, DL Discovery of an exceptionally potent and selective class of fatty acid amide hydrolase inhibitors enlisting proteome-wide selectivity screening: concurrent optimization of enzyme inhibitor potency and selectivity. Bioorg Med Chem Lett15:1423-8 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Liver carboxylesterase 1 |
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Name: | Liver carboxylesterase 1 |
Synonyms: | Acyl coenzyme A:cholesterol acyltransferase | Acyl-CoA: cholesterol acyltransferase (ACAT) | CES1 | CES2 | EST1_HUMAN | SES1 | Serine hydrolase (CES1) |
Type: | Protein |
Mol. Mass.: | 62520.83 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 567 |
Sequence: | MWLRAFILATLSASAAWGHPSSPPVVDTVHGKVLGKFVSLEGFAQPVAIFLGIPFAKPPL
GPLRFTPPQPAEPWSFVKNATSYPPMCTQDPKAGQLLSELFTNRKENIPLKLSEDCLYLN
IYTPADLTKKNRLPVMVWIHGGGLMVGAASTYDGLALAAHENVVVVTIQYRLGIWGFFST
GDEHSRGNWGHLDQVAALRWVQDNIASFGGNPGSVTIFGESAGGESVSVLVLSPLAKNLF
HRAISESGVALTSVLVKKGDVKPLAEQIAITAGCKTTTSAVMVHCLRQKTEEELLETTLK
MKFLSLDLQGDPRESQPLLGTVIDGMLLLKTPEELQAERNFHTVPYMVGINKQEFGWLIP
MQLMSYPLSEGQLDQKTAMSLLWKSYPLVCIAKELIPEATEKYLGGTDDTVKKKDLFLDL
IADVMFGVPSVIVARNHRDAGAPTYMYEFQYRPSFSSDMKPKTVIGDHGDELFSVFGAPF
LKEGASEEEIRLSKMVMKFWANFARNGNPNGEGLPHWPEYNQKEGYLQIGANTQAAQKLK
DKEVAFWTNLFAKKAVEKPPQTEHIEL
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BDBM50073987 |
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n/a |
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Name | BDBM50073987 |
Synonyms: | 1,1,1-Trifluoro-9-phenyl-nonan-2-one | 1,1,1-trifluoro-9-phenylnonan-2-one | CHEMBL91417 |
Type | Small organic molecule |
Emp. Form. | C15H19F3O |
Mol. Mass. | 272.306 |
SMILES | FC(F)(F)C(=O)CCCCCCCc1ccccc1 |
Structure |
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