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TargetMonoglyceride lipase
LigandBDBM50393236
Substrate/Competitorn/a
Meas. Tech.ChEMBL_936102 (CHEMBL2319595)
Temperature298.15±n/a K
IC50 4060±n/a nM
Commentsextracted
Citation Feledziak, MMichaux, CLambert, DMMarchand-Brynaert, J An unprecedented reversible mode of action ofß-lactams for the inhibition of human fatty acid amide hydrolase (hFAAH). Eur J Med Chem60:101-11 (2013) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Monoglyceride lipase
Name:Monoglyceride lipase
Synonyms:HU-K5 | Lysophospholipase homolog | Lysophospholipase-like | MAGL | MGL | MGLL | MGLL_HUMAN
Type:Hydrolase
Mol. Mass.:33264.56
Organism:Homo sapiens (Human)
Description:Human recombinant MGL (Cayman Chemical, cat# 10008354).
Residue:303
Sequence:
MPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEE
LARMLMGLDLLVFAHDHVGHGQSEGERMVVSDFHVFVRDVLQHVDSMQKDYPGLPVFLLG
HSMGGAIAILTAAERPGHFAGMVLISPLVLANPESATTFKVLAAKVLNLVLPNLSLGPID
SSVLSRNKTEVDIYNSDPLICRAGLKVCFGIQLLNAVSRVERALPKLTVPFLLLQGSADR
LCDSKGAYLLMELAKSQDKTLKIYEGAYHVLHKELPEVTNSVFHEINMWVSQRTATAGTA
SPP
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  Blast E-value cutoff:
BDBM50393236
n/a
NameBDBM50393236
Synonyms:CHEMBL2151432
TypeSmall organic molecule
Emp. Form.C20H25NO4
Mol. Mass.343.4168
SMILESC[C@@H](OC(=O)CCCc1ccccc1)[C@@H]1CN(C(=O)CCC=C)C1=O |r|
Structure
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