Reaction Details |
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Target | N-acylethanolamine-hydrolyzing acid amidase |
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Ligand | BDBM50439653 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_978419 (CHEMBL2421061) |
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IC50 | 5.0±n/a nM |
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Citation | Ponzano, S; Bertozzi, F; Mengatto, L; Dionisi, M; Armirotti, A; Romeo, E; Berteotti, A; Fiorelli, C; Tarozzo, G; Reggiani, A; Duranti, A; Tarzia, G; Mor, M; Cavalli, A; Piomelli, D; Bandiera, T Synthesis and structure-activity relationship (SAR) of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters, a class of potent N-acylethanolamine acid amidase (NAAA) inhibitors. J Med Chem56:6917-34 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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N-acylethanolamine-hydrolyzing acid amidase |
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Name: | N-acylethanolamine-hydrolyzing acid amidase |
Synonyms: | ASAH-like protein | ASAHL | Acid ceramidase-like protein | N-acylethanolamine-hydrolyzing acid amidase | N-acylsphingosine amidohydrolase-like | N-acylsphingosine-amidohydrolase | NAAA | NAAA_HUMAN | PLT |
Type: | Enzyme |
Mol. Mass.: | 40073.12 |
Organism: | Homo sapiens (Human) |
Description: | Q02083 |
Residue: | 359 |
Sequence: | MRTADREARPGLPSLLLLLLAGAGLSAASPPAAPRFNVSLDSVPELRWLPVLRHYDLDLV
RAAMAQVIGDRVPKWVHVLIGKVVLELERFLPQPFTGEIRGMCDFMNLSLADCLLVNLAY
ESSVFCTSIVAQDSRGHIYHGRNLDYPFGNVLRKLTVDVQFLKNGQIAFTGTTFIGYVGL
WTGQSPHKFTVSGDERDKGWWWENAIAALFRRHIPVSWLIRATLSESENFEAAVGKLAKT
PLIADVYYIVGGTSPREGVVITRNRDGPADIWPLDPLNGAWFRVETNYDHWKPAPKEDDR
RTSAIKALNATGQANLSLEALFQILSVVPVYNNFTIYTTVMSAGSPDKYMTRIRNPSRK
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BDBM50439653 |
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n/a |
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Name | BDBM50439653 |
Synonyms: | CHEMBL2419830 | US9353075, 35 |
Type | Small organic molecule |
Emp. Form. | C16H27NO4 |
Mol. Mass. | 297.3899 |
SMILES | C[C@@H]1OC(=O)[C@@H]1NC(=O)OCCCCCC1CCCCC1 |r| |
Structure |
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