Zhu Yuyao, Zhang Jian, Huang Xiaode, Chen Bin, Qian Hua, Zhao Botao
Nanjing Research Institute for Comprehensive Utilization of Wild Plants, Nanjing 210042, P.R. China.
Key Laboratory of Modern Chinese Medicines, China Pharmaceutical University, Nanjing 210038, P.R. China.
J Microbiol Biotechnol. 2018 Nov 28;28(11):1876-1882. doi: 10.4014/jmb.1804.04042.
A series of pentacyclic triterpenoids similar to glycyrrhetinic acid were designed and synthesized via the combination of chemical modification and microbial catalysis. All products were screened for the glycogen phosphorylases inhibitory activities in vitro. Within this series of derivatives, compound displayed good inhibitory activities with IC value of 27.7 μM, which is better than that of the other derivatives and glycyrrhetinic acid. Structure-activity relationship (SAR) analysis of these inhibitors was also discussed.
通过化学修饰和微生物催化相结合的方法,设计并合成了一系列与甘草次酸类似的五环三萜类化合物。对所有产物进行了体外糖原磷酸化酶抑制活性筛选。在这一系列衍生物中,化合物显示出良好的抑制活性,IC值为27.7 μM,优于其他衍生物和甘草次酸。还讨论了这些抑制剂的构效关系(SAR)分析。