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Substrate Report for: 1-Naphtylpropionate

General
Type Propionate, Naphtyl ester, Aromatic ester (two rings), Naphthalen
Chemical_Nomenclature naphthalen-1-yl propanoate
Canonical SMILES CCC(=O)OC1=CC=CC2=CC=CC=C21
InChI InChI=1S/C13H12O2/c1-2-13(14)15-12-9-5-7-10-6-3-4-8-11(10)12/h3-9H,2H2,1H3
InChIKey FRXPDEZCWCPLIH-UHFFFAOYSA-N
Other name(s) 1-Naphthyl propionate ; Naphthalen-1-yl propionate ; Propionic acid 1-naphthyl ester ; alpha-NPr ; ZINC363535 ; SCHEMBL448000 ; C3-naphthyl ester
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MW|200.23
Formula|C13H12O2
CAS_number|3121-71-9
PubChem|76572
UniChem|FRXPDEZCWCPLIH-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target
Families | 1-Naphtylpropionate ligand of proteins in family: AlphaBeta_hydrolase, Carb_B_Arthropoda, FaeC, Tannase
Protein | lacjo-q74hk5, aphgo-cxest, aspor-faec, aspor-q2uf27

References:
Search PubMed for references concerning: 1-Naphtylpropionate

1 more
    Title: Identification and characterization of an acetyl xylan esterase from Aspergillus oryzae
    Kato T, Shiono Y, Koseki T
    Ref: J Biosci Bioeng, :, 2021 : PubMed

            

    Title: An inserted alpha/beta subdomain shapes the catalytic pocket of Lactobacillus johnsonii cinnamoyl esterase
    Lai KK, Stogios PJ, Vu C, Xu X, Cui H, Molloy S, Savchenko A, Yakunin A, Gonzalez CF
    Ref: PLoS ONE, 6:e23269, 2011 : PubMed

            

    Title: Carboxylesterase activity, cDNA sequence, and gene expression in malathion susceptible and resistant strains of the cotton aphid, Aphis gossypii
    Pan Y, Guo H, Gao X
    Ref: Comparative Biochemistry & Physiology B Biochem Mol Biol, 152:266, 2009 : PubMed