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Studies on methyl xestopongoate analogues:design, synthesis and antitumor activities / 中国药科大学学报
Article in Zh | WPRIM | ID: wpr-811738
Responsible library: WPRO
ABSTRACT
@#Fifty-two methyl xestospongoate analogues were designed, synthesized and evaluated for the antiproliferative activity. Starting from alkynyl methyl ester and diyne, methyl xestospongoate analogues 4(a-m)-7(a-m)were synthesized by Cadiot-Chodkiewitz coupling and Sonogashira coupling reactions. Their structures were identified by 1H NMR, 13C NMR and HREI-MS. The cytotoxic inhibiton activities in vitro of some compounds were evaluated against human cancer cells A549 and P-388 by a CCK-8 method. Among them, compound 6k exhibited potent cell growth inhibitory activity against A549 and P-388 cancer cells, with IC50 values of 9. 36 and 9. 62 μmol/L, respectively.
Key words
Full text: 1 Database: WPRIM Language: Zh Journal: Journal of China Pharmaceutical University Year: 2018 Document type: Article
Full text: 1 Database: WPRIM Language: Zh Journal: Journal of China Pharmaceutical University Year: 2018 Document type: Article