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Regioselective Enzymatic Synthesis of Non-Steroidal Anti-Inflammatory Drugs Containing Glucose in Organic Media
Authors:Na?Wang,Bo?Kai?Liu,Qi?Wu,Jun?Liang?Wang,Xian?Fu?Lin  author-information"  >  author-information__contact u-icon-before"  >  mailto:llc@zju.edu.cn"   title="  llc@zju.edu.cn"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Department of Chemistry, Zhejiang University, 310027 Hangzhou, P.R. China
Abstract:Enzymatic transesterification of glucose with the vinyl ester of non-steroidal anti-inflammatory drugs (NSAIDs) was in organic media performed for synthesis of novel NSAIDs-glucose conjugates. Glucose was regioselectively acylated at the 6-hydroxyl group. The indomethacin-glucose conjugate and ketoprofen-glucose conjugate were produced by the catalysis of alkaline protease from Bacillus subtilis in the respective yields of 42% (over 48 h) and 63% (over 40 h). The etodolac-glucose conjugate was obtained in 26% yield (over 144 h) by lipase from Candida antarctica.
Keywords:enzymatic synthesis  glucose  non-steroidal anti-inflammatory drugs  regioselectivity  transesterification
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