Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
Yuanfang Kong1, Jindan Xu1,2,3, Pengbo Zhu1,2,3
1Henan University of Chinese Medicine Zhengzhou 450046 Henan China kongyf@hactcm.edu.cn jyzhang2004@126.com chunhong_dong@hactcm.edu.cn.
Abstract:
Iridoid glycoside, which belongs to the polyhydroxy compound, is a kind of active ingredient of traditional Chinese medicine with a wide range of sources, and has many pharmacological effects such as anti-cancer, anti-inflammatory, anti-virus, hypoglycemic and so on. Its structure contains many hydroxyl groups, including two primary hydroxyl groups. The chemical reactivity of primary hydroxyl groups has very little difference, so it is very important to control the selectivity of hydroxyl groups under certain conditions. In this paper, the difference between the two primary hydroxyl groups in iridoid glycoside was calculated based on computer simulation and verified this result through designed experiments. This study will provide an important way for site-directed modification of hydroxyl in iridoid glycoside in the future.
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