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TargetN-acylethanolamine-hydrolyzing acid amidase
LigandBDBM50577376
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2130034 (CHEMBL4839463)
IC50 330±n/a nM
Citation Di Fruscia, PCarbone, ABottegoni, GBerti, FGiacomina, FPonzano, SPagliuca, CFiasella, APizzirani, DOrtega, JANuzzi, ATarozzo, GMengatto, LGiampà, RPenna, IRusso, DRomeo, ESumma, MBertorelli, RArmirotti, ABertozzi, SMReggiani, ABandiera, TBertozzi, F Discovery and SAR Evolution of Pyrazole Azabicyclo[3.2.1]octane Sulfonamides as a Novel Class of Non-Covalent  J Med Chem64:13327-13355 (2021) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
N-acylethanolamine-hydrolyzing acid amidase
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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  Blast E-value cutoff:
BDBM50577376
n/a
NameBDBM50577376
Synonyms:CHEMBL4866583
TypeSmall organic molecule
Emp. Form.C16H23N5O3S
Mol. Mass.365.451
SMILESCCCc1n[nH]c(C)c1S(=O)(=O)N1CCC(CC1)Oc1cnccn1
Structure
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