中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis and antitumor activity of a series of lactone-opened camptothecin derivatives

文献类型:期刊论文

作者Zheng, Chao3; Li, Ming-Zong2; You, Tian-Pa2; Tang, Wei-Ping1; Lou, Li-Guang1
刊名Journal of Asian natural products research
出版日期2017-10-24
页码1-11
ISSN号1477-2213
DOI10.1080/10286020.2017.1392941
文献子类Article
英文摘要A series of E-ring lactone-opened camptothecin (CPT) derivatives bearing with terminal aza-heterocyclic groups were synthesized, and their antitumor activity was evaluated both in vitro and in vivo. Hydroxyl-amide analogues with morpholin-4-yl displayed excellent antitumor activity in vitro and efficient inhibition on tumor xenograph model in nude mice. Ester-amide compounds acted less active in vitro cytotoxicity and lower inhibition activity in vivo. Substitutions at 7- and 10- positions favored the antitumor activity.
语种英语
源URL[http://119.78.100.183/handle/2S10ELR8/266788]  
专题药理学第一研究室
作者单位1.c Shanghai Institute of Materia Medica, Chinese Academy of Science , Shanghai 201203 , China
2.b Department of Chemistry , University of Science & Technology of China , Hefei 230026 , China;
3.a Key Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, Collaborative Innovation Center of Tropical Biological Resources , Hainan Normal University , Haikou 571158 , China;
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GB/T 7714
Zheng, Chao,Li, Ming-Zong,You, Tian-Pa,et al. Synthesis and antitumor activity of a series of lactone-opened camptothecin derivatives[J]. Journal of Asian natural products research,2017:1-11.
APA Zheng, Chao,Li, Ming-Zong,You, Tian-Pa,Tang, Wei-Ping,&Lou, Li-Guang.(2017).Synthesis and antitumor activity of a series of lactone-opened camptothecin derivatives.Journal of Asian natural products research,1-11.
MLA Zheng, Chao,et al."Synthesis and antitumor activity of a series of lactone-opened camptothecin derivatives".Journal of Asian natural products research (2017):1-11.

入库方式: OAI收割

来源:上海药物研究所

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