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作 者:Yan Wu Wei-Qi Chen Yu-Qing Zhao Hu-Ri Piao
机构地区:[1]Key Laboratory of Natural Resources and Functional Molecules of the Changbai Mountain,Affiliated Ministry of Education,Yanbian University College of Pharmacy [2]Department of Chemistry,Fudan University [3]School of Traditional Chinese Materia Medica,Shenyang Pharmaceutical University
出 处:《Chinese Chemical Letters》2015年第3期334-338,共5页中国化学快报(英文版)
基 金:supported by the National Natural Science Foundation of China (Nos.81160381 and 81260468);the Natural Science Foundation of Jilin Province (No.201115235)
摘 要:An efficient method has been developed for the synthesis of a series of(20R)-panaxadiol derivatives(4a–w) using a continuous-flow microreactor.The antitumor activities of the newly synthesized compounds were evaluated in vitro in two human prostate adenocarcinoma tumor cell lines(i.e.,PC-3and LNCa P cells),and their cytotoxicities were evaluated using a standard MTT assay.Compounds 4c,4h,4p,4q and 4s exhibited higher antitumor activities toward PC-3 cell line than panaxadiol,which was used as a reference standard.An efficient method has been developed for the synthesis of a series of(20R)-panaxadiol derivatives(4a–w) using a continuous-flow microreactor.The antitumor activities of the newly synthesized compounds were evaluated in vitro in two human prostate adenocarcinoma tumor cell lines(i.e.,PC-3and LNCa P cells),and their cytotoxicities were evaluated using a standard MTT assay.Compounds 4c,4h,4p,4q and 4s exhibited higher antitumor activities toward PC-3 cell line than panaxadiol,which was used as a reference standard.
关 键 词:antitumor adenocarcinoma toward silica batch shorter spectrometer incubated equiv acetate
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