| Reaction Details |
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 | Report a problem with these data |
| Target | Monoglyceride lipase |
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| Ligand | BDBM50255806 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEBML_1687487 |
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| IC50 | 6.0±n/a nM |
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| Citation |  McAllister, LA; Butler, CR; Mente, S; O'Neil, SV; Fonseca, KR; Piro, JR; Cianfrogna, JA; Foley, TL; Gilbert, AM; Harris, AR; Helal, CJ; Johnson, DS; Montgomery, JI; Nason, DM; Noell, S; Pandit, J; Rogers, BN; Samad, TA; Shaffer, CL; da Silva, RG; Uccello, DP; Webb, D; Brodney, MA Discovery of Trifluoromethyl Glycol Carbamates as Potent and Selective Covalent Monoacylglycerol Lipase (MAGL) Inhibitors for Treatment of Neuroinflammation. J Med Chem61:3008-3026 (2018) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Monoglyceride lipase |
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| Name: | Monoglyceride lipase |
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| Synonyms: | HU-K5 | Lysophospholipase homolog | Lysophospholipase-like | MAGL | MGL | MGLL | MGLL_HUMAN |
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| Type: | Hydrolase |
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| Mol. Mass.: | 33264.56 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Human recombinant MGL (Cayman Chemical, cat# 10008354). |
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| Residue: | 303 |
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| Sequence: | MPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEE
LARMLMGLDLLVFAHDHVGHGQSEGERMVVSDFHVFVRDVLQHVDSMQKDYPGLPVFLLG
HSMGGAIAILTAAERPGHFAGMVLISPLVLANPESATTFKVLAAKVLNLVLPNLSLGPID
SSVLSRNKTEVDIYNSDPLICRAGLKVCFGIQLLNAVSRVERALPKLTVPFLLLQGSADR
LCDSKGAYLLMELAKSQDKTLKIYEGAYHVLHKELPEVTNSVFHEINMWVSQRTATAGTA
SPP
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| BDBM50255806 |
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| n/a |
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| Name | BDBM50255806 |
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| Synonyms: | CHEMBL4097100 |
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| Type | Small organic molecule |
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| Emp. Form. | C18H17F4N3O3 |
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| Mol. Mass. | 399.3395 |
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| SMILES | [H][C@@]12CN(C[C@]1([H])[C@H]2c1ccn(n1)-c1ccc(F)cc1)C(=O)OC(CO)C(F)(F)F |r| |
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| Structure | 
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