Design, Synthesis and Antitumor Activity of Pyrrolopyrazinone-chalcone Hybrids
Design, Synthesis and Antitumor Activity of Pyrrolopyrazinone-chalcone Hybrids作者机构:10016 P. R. China Key Laboratory for Molecular Enzymology & Engineering Ministry of Education Jilin University Changchun 130012 P. R. China
出 版 物:《Chemical Research in Chinese Universities》 (高等学校化学研究(英文版))
年 卷 期:2014年第30卷第4期
页 面:624-631页
核心收录:
学科分类:1007[医学-药学(可授医学、理学学位)] 081302[工学-建筑设计及其理论] 08[工学] 0813[工学-建筑学] 10[医学]
基 金:Supported by the Program for Liaoning Innovative Research Team in University China
主 题:Pyrrolopyrazinone-chalcone hybrid Antitumor Marine sponge Combination principle
摘 要:A series of pyrrolopyrazinone-chalcone hybrids(12a-12q) was designed,synthesized and screened for their antitumor activity against SKOV-3,A549 and HeLa cell lines in *** with the pyrrolopyrazinone(10a) and 5-fluorouracil(5-FU),nearly all the tested compounds showed significantly-improved antitumor *** most promising compounds 12e and 12k(IC50=0.25 and 0.88 μmol/L) respectively show activities of 123and 35 times that of compound 10a(IC50=30.74 μmol/L) against HeLa cell *** result reveals that the presence of chalcone moiety is beneficial to their activity and selectivity.