化学
阿司匹林
消炎药
药理学
药品
组合化学
立体化学
生物化学
医学
作者
Keli Gu,Lanrong Bi,Ming Zhao,Chao Wang,Jingfang Ju,Shiqi Peng
标识
DOI:10.1016/j.bmc.2007.05.013
摘要
A new class of 2,5-disubstituted-dioxacycloalkanes were designed and synthesized via stereoselective synthetic method as cancer chemoprevention agents. The anti-inflammatory activities of these compounds were tested using the xylene-induced mouse ear edema model. Some of these compounds exhibited comparable or better anti-inflammatory activities than that of aspirin suggesting that they can be further developed as potential anti-inflammatory drug lead compounds. In addition, treatment of these anti-inflammatory agents did not prolong tail bleeding time in mice. The structure/activity relationships were also analyzed among these compounds.
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