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- W2012309741 abstract "A series of N-benzylgalactonoamidines was synthesized to probe their inhibitory ability during the hydrolysis of o-nitrophenyl-β-d-galactopyranoside by β-galactosidase (Aspergillus oryzae). All compounds are characterized as potent competitive inhibitors with inhibition constants (Ki) in the low nanomolar range (12–48 nM). The structure of the inhibitors mimics the bond-lengthening during the hydrolysis and the aromatic aglycon of the substrate. The electronic nature of the substituent in p-position of the aglycon influences the overall inhibitory ability most when compared to the unsubstituted parent compound." @default.
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- W2012309741 date "2012-01-01" @default.
- W2012309741 modified "2023-09-26" @default.
- W2012309741 title "N-Benzylgalactonoamidines as potent β-galactosidase inhibitors" @default.
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- W2012309741 doi "https://doi.org/10.1016/j.tet.2011.10.048" @default.
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