摘要

The biotransformation of a pentacyclic triterpene, oleanolic acid (1), with Fusarium lini afforded two oxidative metabolites, 2,3-dihydroxyolean-12-en-28-oic acid (2), and 2,3,11-trihydroxyolean-12-en-28-oic acid (3). Metabolite 3 was found to be a new compound. The structures were characterized on the basis of spectroscopic studies. These metabolites exhibited a potent inhibition of -glucosidase enzyme.

  • 出版日期2008