Design, synthesis, and biological evaluation of urolithin derivatives as potential phosphodiesterase II inhibitors

被引:0
|
作者
Wang, Hecheng [1 ]
Tang, Long [1 ]
Di, Wanhui [1 ]
Yan, Feng [1 ]
Huang, Xianfeng [1 ]
Feng, Xiaoqing [1 ,2 ]
Song, Guoqiang [1 ,2 ]
机构
[1] Changzhou Univ, Sch Pharmaceut Engn & Life Sci, Changzhou, Peoples R China
[2] Changzhou Univ, Sch Pharmaceut Engn & Life Sci, Changzhou 213164, Peoples R China
关键词
biological activity; inhibitors; PDE2; urolithins; ELLAGIC ACID; ELLAGITANNINS; METABOLISM; BINDING;
D O I
10.1177/17475198221148080
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Urolithins are the gut microbiota metabolites of ellagitannins which are found in natural plants such as pomegranate, strawberry, and raspberry, and in nuts. Recently, several reports have clarified the underlying mechanism of urolithins in central nervous system inflammation. Therefore, urolithins have become potential therapeutic drug candidate molecules for central nervous system diseases. Derivatives 1-1d, 1-1f, 3-2a, and 3-2b of urolithin A, urolithin B, and methoxyurolithin A were found to have had significant inhibitory activity against phosphodiesterase II with IC50 values of 35.42, 39.96, 25.58, and 13.84 & mu;M, respectively. Herein, we report the design and synthesis of urolithin derivatives along with a biological evaluation of their activity against phosphodiesterase II.
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页数:17
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