摘要
The discovery of a-glucosidase inhibitors has been actively pursued with the aim to develop therapeutics for the treatment of diabetes and other carbohydrate-mediated diseases. This study focused on the lichen Cladonia sp., which yielded three potent a-glucosidase inhibitors, namely zeorin (1), methyl alpha-orcinolcarboxylate (2) and rnethylorsellinate (3) with several fold higher inhibitory activities than those of acarbose, an antidiabetic drug used to manage type II diabetes mellitus and the standard, 1-deoxynojirimycin, Atranorin (4) and lobaric acid (5), the other two metabolites isolated from the lichen did not show any alpha-glucosidase inhibitory potential. All compounds were identified on the basis of one dimentional (1D) and two dimentional (2D) NMR spectral data and with comparison to reported data.
- 出版日期2014-3