Vitamin E glycosides were synthesized and enzymatic hydrolysis was examined for use as potential prodrugs, however, the glycoside bond was found to be stable. On the other hand, among the glycosides synthesized, dl-α-tocopherylglucoside (6b) and dl-α-tococopherylmannoside (6c) showed strong inhibitory action on histamine release from mast cells. In addition, 6c also showed a suppressive action on IgE antibody formation. Thus, tocopheryl glycoside showed new properties compared to tocopherol (vitamin E). In particular, 6c was shown to be a novel lead compound with excellent manifold anti-allergic activity and anti-inflammatory activity.
CITATION STYLE
Satoh, T., Miyataka, H., Yamamoto, K., & Hirano, T. (2001). Synthesis and physiological activity of novel tocopheryl glycosides. Chemical and Pharmaceutical Bulletin, 49(8), 948–953. https://doi.org/10.1248/cpb.49.948
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