Synthesis and tumor cytotoxicity of novel 1,2,3-triazole-substituted 3-oxo-oleanolic acid derivatives

Fengran Li , Yang Liu , Shuai Wang , Gaofei Wei , Maosheng Cheng

Chemical Research in Chinese Universities ›› 2016, Vol. 32 ›› Issue (6) : 938 -942.

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Chemical Research in Chinese Universities ›› 2016, Vol. 32 ›› Issue (6) : 938 -942. DOI: 10.1007/s40242-016-6301-5
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Synthesis and tumor cytotoxicity of novel 1,2,3-triazole-substituted 3-oxo-oleanolic acid derivatives

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Abstract

Fifteen novel 3-oxo-oleanolic acid esters bearing aryl substituted 1,2,3-triazolyl methyl moiety were synthesized via the method of Copper(I)-catalyzed Huisgen cycloaddition. The cytotoxicity evaluation results of these compounds against five human tumor cell lines show that most of these compounds presented potent activity and selectivity against A375-S2 and HT1080 cells. Compound 6c, with a p-NO2 at the bezene ring, possesses the best inhibitory activity against A375-S2(IC50=2.82 μmol/L) and HT1080(IC50=1.69 μmol/L).

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3-Oxo-oleanolic acid / 1,2,3-Triazole / Tumor cytotoxicity

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Fengran Li, Yang Liu, Shuai Wang, Gaofei Wei, Maosheng Cheng. Synthesis and tumor cytotoxicity of novel 1,2,3-triazole-substituted 3-oxo-oleanolic acid derivatives. Chemical Research in Chinese Universities, 2016, 32(6): 938-942 DOI:10.1007/s40242-016-6301-5

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