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TargetMonoglyceride lipase
LigandBDBM50562160
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2077554 (CHEMBL4733345)
IC50 18±n/a nM
Citation Granchi, CBononi, GFerrisi, RGori, EMantini, GGlasmacher, SPoli, GPalazzolo, SCaligiuri, IRizzolio, FCanzonieri, VPerin, TGertsch, JSodi, AGiovannetti, EMacchia, MMinutolo, FTuccinardi, TChicca, A Design, synthesis and biological evaluation of second-generation benzoylpiperidine derivatives as reversible monoacylglycerol lipase (MAGL) inhibitors. Eur J Med Chem209:0 (2021) [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:
BDBM50562160
n/a
NameBDBM50562160
Synonyms:CHEMBL4757403
TypeSmall organic molecule
Emp. Form.C25H21F2NO3S
Mol. Mass.453.501
SMILESOc1cc(C(=O)N2CCC(CC2)C(=O)c2ccc(Sc3ccccc3)cc2)c(F)cc1F
Structure
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