Reaction Details |
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Target | N-acylethanolamine-hydrolyzing acid amidase |
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Ligand | BDBM50416509 |
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Substrate/Competitor | BDBM223534 |
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Meas. Tech. | NAAA Assay |
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pH | 5±n/a |
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Temperature | 310.15±n/a K |
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IC50 | 420±20 nM |
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Comments | extracted |
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Citation | Piomelli, D; Tarzia, G; Mor, M; Duranti, A; Tontini, A Compositions and methods of inhibiting N-acylethanolamine-hydrolyzing acid amidase US Patent US9321743 Publication Date 4/26/2016 |
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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 | N-acylethanolamine acid amidase (NAAA) | N-acylethanolamine-hydrolyzing acid amidase | N-acylethanolamine-hydrolyzing acid amidase (NAAA) | N-acylethanolamine-hydrolyzing acid amidase subunit alpha | N-acylethanolamine-hydrolyzing acid amidase subunit beta | N-acylsphingosine amidohydrolase-like | NAAA_RAT | Naaa |
Type: | Enzyme |
Mol. Mass.: | 40306.53 |
Organism: | Rattus norvegicus (Rat) |
Description: | Q5KTC7 |
Residue: | 362 |
Sequence: | MGTPAIRAACHGAHLALALLLLLSLSDPWLWATAPGTPPLFNVSLDAAPELRWLPMLQHY
DPDFVRAAVAQVIGDRVPQWILEMIGEIVQKVESFLPQPFTSEIRGICDYLNLSLAEGVL
VNLAYEASAFCTSIVAQDSQGRIYHGRNLDYPFGNALRKLTADVQFVKNGQIVFTATTFV
GYVGLWTGQSPHKFTISGDERDKGWWWENMIAALSLGHSPISWLIRKTLTESEDFEAAVY
TLAKTPLIADVYYIVGGTSPQEGVVITRDRGGPADIWPLDPLNGAWFRVETNYDHWEPVP
KRDDRRTPAIKALNATGQAHLSLETLFQVLSVFPVYNNYTIYTTVMSAAEPDKYMTMIRN
PS
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BDBM50416509 |
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BDBM223534 |
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Name | BDBM50416509 |
Synonyms: | CHEMBL1214256 | US9321743, URB783 |
Type | Small organic molecule |
Emp. Form. | C12H13NO3 |
Mol. Mass. | 219.2365 |
SMILES | O=C(CCc1ccccc1)N[C@H]1COC1=O |r| |
Structure |
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