Reaction Details |
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Target | N-acylethanolamine-hydrolyzing acid amidase |
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Ligand | BDBM393371 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1977317 (CHEMBL4610452) |
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IC50 | 12±n/a nM |
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Citation | Malamas, MS; Farah, SI; Lamani, M; Pelekoudas, DN; Perry, NT; Rajarshi, G; Miyabe, CY; Chandrashekhar, H; West, J; Pavlopoulos, S; Makriyannis, A Design and synthesis of cyanamides as potent and selective N-acylethanolamine acid amidase inhibitors. Bioorg Med Chem28:0 (2020) [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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BDBM393371 |
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n/a |
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Name | BDBM393371 |
Synonyms: | 3-((4-(Pyridin-3-yl)benzyl)oxy)azetidine-1-carbonitrile | US9963444, Example 72 |
Type | Small organic molecule |
Emp. Form. | C16H15N3O |
Mol. Mass. | 265.3098 |
SMILES | N#CN1CC(C1)OCc1ccc(cc1)-c1cccnc1 |
Structure |
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