Rezende, Sebastião T. deViana, Pollyanna A.Alves, Arianne de A.Manfrini, Rozângela M.Alves, Ricardo J.Bemquerer, Marcelo P.Santoro, Marcelo M.Guimarães, Valéria M.2018-05-292018-05-292011-04-0100086215https://doi.org/10.1016/j.carres.2011.01.024http://www.locus.ufv.br/handle/123456789/19851α-d-Galactopyranosides were synthesized and their inhibitory activities toward the Debaryomyces hansenii UFV-1 extracellular and intracellular α-galactosidases were evaluated. Methyl α-d-galactopyranoside was the most potent inhibitor compared to the others tested, with values of 0.82 and 1.12 mmol L−1, for extracellular and intracellular enzymes, respectively. These results indicate that the presence of a hydroxyl group in the C-6 position of α-d-galactopyranoside derivatives is important for the recognition by D. hansenii UFV-1 α-galactosidases.pdfengElsevier Ltd.α-GalactosidasesDebaryomyces hansenii UFV-1α-d-Galactopyranoside derivativesInhibitionArtigo