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Reaction Details
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TargetLysosomal acid lipase/cholesteryl ester hydrolase
LigandBDBM50287472
Substrate/Competitorn/a
Meas. Tech.ChEBML_154781
IC50 10000±n/a nM
Citation David, BSchuber, F Synthesis of α-difluoro and α-difluoro-β-trifluoroketo-derivatives as potential inhibitors for Cholesterol Ester Hydrolase Bioorg Med Chem Lett6:1673-1676 (1996)    Article
More Info.:Get all data from this article,  Assay Method
 
Lysosomal acid lipase/cholesteryl ester hydrolase
Name:Lysosomal acid lipase/cholesteryl ester hydrolase
Synonyms:LICH_HUMAN | LIPA
Type:PROTEIN
Mol. Mass.:45422.01
Organism:Homo sapiens (Human)
Description:ChEMBL_633497
Residue:399
Sequence:
MKMRFLGLVVCLVLWTLHSEGSGGKLTAVDPETNMNVSEIISYWGFPSEEYLVETEDGYI
LCLNRIPHGRKNHSDKGPKPVVFLQHGLLADSSNWVTNLANSSLGFILADAGFDVWMGNS
RGNTWSRKHKTLSVSQDEFWAFSYDEMAKYDLPASINFILNKTGQEQVYYVGHSQGTTIG
FIAFSQIPELAKRIKMFFALGPVASVAFCTSPMAKLGRLPDHLIKDLFGDKEFLPQSAFL
KWLGTHVCTHVILKELCGNLCFLLCGFNERNLNMSRVDVYTTHSPAGTSVQNMLHWSQAV
KFQKFQAFDWGSSAKNYFHYNQSYPPTYNVKDMLVPTAVWSGGHDWLADVYDVNILLTQI
TNLVFHESIPEWEHLDFIWGLDAPWRLYNKIINLMRKYQ
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50287472
n/a
NameBDBM50287472
Synonyms:1-((S)-10,13-Dimethyl-17-octyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl)-3,3,4,4,4-pentafluoro-butan-2-one | CHEMBL3137812
TypeSmall organic molecule
Emp. Form.C31H49F5O
Mol. Mass.532.7122
SMILES[H][C@@]12CCC(CCCCCCCC)C1(C)CC[C@@]1([H])[C@@]2([H])CCC2C[C@@H](CC(=O)C(F)(F)C(F)(F)F)CCC12C
Structure
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