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TargetLysosomal acid lipase/cholesteryl ester hydrolase
LigandBDBM50318692
Substrate/Competitorn/a
Meas. Tech.ChEMBL_633497 (CHEMBL1119694)
IC50 473±n/a nM
Citation Rosenbaum, AICosner, CCMariani, CJMaxfield, FRWiest, OHelquist, P Thiadiazole carbamates: potent inhibitors of lysosomal acid lipase and potential Niemann-Pick type C disease therapeutics. J Med Chem53:5281-9 (2010) [PubMed]  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
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  Blast E-value cutoff:
BDBM50318692
n/a
NameBDBM50318692
Synonyms:4-(Pyrrolidin-1-yl)-1,2,5-thiadiazol-3-yl morpholine-4-carboxylate | CHEMBL1085856
TypeSmall organic molecule
Emp. Form.C11H16N4O3S
Mol. Mass.284.335
SMILESO=C(Oc1nsnc1N1CCCC1)N1CCOCC1
Structure
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