| Reaction Details |
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 | Report a problem with these data |
| Target | N-acylethanolamine-hydrolyzing acid amidase |
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| Ligand | BDBM50234742 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_1653844 (CHEMBL4003210) |
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| IC50 | 17±n/a nM |
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| Citation |  Petracca, R; Ponzano, S; Bertozzi, SM; Sasso, O; Piomelli, D; Bandiera, T; Bertozzi, F Progress in the development of฿-lactams as N-Acylethanolamine Acid Amidase (NAAA) inhibitors: Synthesis and SAR study of new, potent N-O-substituted derivatives. Eur J Med Chem126:561-575 (2017) [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 |
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| 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 |
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| Type: | Enzyme |
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| Mol. Mass.: | 40073.12 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Q02083 |
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| Residue: | 359 |
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| Sequence: | MRTADREARPGLPSLLLLLLAGAGLSAASPPAAPRFNVSLDSVPELRWLPVLRHYDLDLV
RAAMAQVIGDRVPKWVHVLIGKVVLELERFLPQPFTGEIRGMCDFMNLSLADCLLVNLAY
ESSVFCTSIVAQDSRGHIYHGRNLDYPFGNVLRKLTVDVQFLKNGQIAFTGTTFIGYVGL
WTGQSPHKFTVSGDERDKGWWWENAIAALFRRHIPVSWLIRATLSESENFEAAVGKLAKT
PLIADVYYIVGGTSPREGVVITRNRDGPADIWPLDPLNGAWFRVETNYDHWKPAPKEDDR
RTSAIKALNATGQANLSLEALFQILSVVPVYNNFTIYTTVMSAGSPDKYMTRIRNPSRK
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| BDBM50234742 |
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| n/a |
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| Name | BDBM50234742 |
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| Synonyms: | CHEMBL4096232 |
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| Type | Small organic molecule |
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| Emp. Form. | C23H32N2O6 |
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| Mol. Mass. | 432.51 |
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| SMILES | COC(=O)c1ccc(ON2[C@@H](C)[C@H](NC(=O)OCCCCC3CCCCC3)C2=O)cc1 |r| |
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| Structure | 
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