摘要
目的合成7-[(2-羟基-3-哌啶)-丙氧基]-异黄酮衍生物。方法以2-位取代的异黄酮与环氧氯丙烷反应,再与哌啶反应,得目标化合物。结果与结论合成了5个目标化合物,经结构确证、药理活性测定,均具有一定的抗肿瘤活性。
OBJECTIVE To synthesize 7 - [ ( 2 - hydroxyl - 3 - piperidino) - propoxy ] - derivaties of isoflavone. METHODS The target compounds were synthesized through the 2 - substitutied isoflavone reaction with epichlorhydrin, and then reacting with piperidine. RESULTS and CONCLUSION Five target compounds were synthesized and they all have some activities against cancer through the pharmacological activity' s determination.
出处
《华西药学杂志》
CAS
CSCD
北大核心
2007年第6期626-629,共4页
West China Journal of Pharmaceutical Sciences
基金
国家科技部973计划项目(2004CB518800)
关键词
异黄酮
环氧氯丙烷
合成
肿瘤
Isoflavone
Epichlorohydrin
Synthesis
Cancer