Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
21322 | Journal of Bioscience and Bioengineering | 2012 | 4 Pages |
Abstract
2-O-α-d-Glucopyranosyl-6-O-(2-pentylheptanoyl)-l-ascorbic acid (6-bDode-AA-2G) underwent an intramolecular acyl migration to yield approximately 12% of 2-O-α-d-glucopyranosyl-5-O-(2-pentylheptanoyl)-l-ascorbic acid (5-bDode-AA-2G) in neutral solutions for 3 days. In small intestine homogenate from guinea pigs for 12 h, 6-bDode-AA-2G, which hardly underwent acyl migration to give 5-bDode-AA-2G, was predominantly hydrolyzed with α-glucosidase and then with esterase to ascorbic acid.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Akihiro Tai, Sayoko Ikeda, Futoshi Yazama, Hideyuki Ito,