中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis, Cytoprotective and Anti-tumor Activities of Isatin Schiff Bases

文献类型:期刊论文

作者Chen, Gang1,2; Meng, Mei1; Zhang, Yu2; Hao, Xiaojiang2,3,4; Wang, Ye3,4; Mu, Shuzhen3,4
刊名LETTERS IN DRUG DESIGN & DISCOVERY
出版日期2015
卷号12期号:10页码:802-805
关键词Isatin synthesis schiff base structure cytoprotective anti-tumor
英文摘要A series of simple isatin Schiff bases were synthesized through the condensation reaction. These isatin Schiff bases were characterized by NMR and MS, and the structure was discussed. Then, the cytoprotective and anti-tumor activities of these compounds were evaluated. The results show that several compounds show protection activity on the apoptosis of PC12 cells induced by H2O2, which are more effective than that of (+/-) alpha-Tocophreol (VE) and isatin. Besides, some compounds also show more potent anti-tumor activity against A549 and P388 cell lines than that of isatin.
类目[WOS]Chemistry, Medicinal
研究领域[WOS]Pharmacology & Pharmacy
关键词[WOS]DERIVATIVES ; ANTICANCER ; DESIGN ; POTENT
收录类别SCI
语种英语
WOS记录号WOS:000364520600002
公开日期2016-02-26
源URL[http://ir.kib.ac.cn/handle/151853/25236]  
专题昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室
作者单位1.Xian Shiyou Univ, Coll Chem & Chem Engn, Xian 701165, Shaanxi, Peoples R China
2.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650204, Peoples R China
3.Key Lab Chem Nat Prod Guizhou Prov, Guiyang 550002, Peoples R China
4.Chinese Acad Sci, Guiyang 550002, Peoples R China
推荐引用方式
GB/T 7714
Chen, Gang,Meng, Mei,Zhang, Yu,et al. Synthesis, Cytoprotective and Anti-tumor Activities of Isatin Schiff Bases[J]. LETTERS IN DRUG DESIGN & DISCOVERY,2015,12(10):802-805.
APA Chen, Gang,Meng, Mei,Zhang, Yu,Hao, Xiaojiang,Wang, Ye,&Mu, Shuzhen.(2015).Synthesis, Cytoprotective and Anti-tumor Activities of Isatin Schiff Bases.LETTERS IN DRUG DESIGN & DISCOVERY,12(10),802-805.
MLA Chen, Gang,et al."Synthesis, Cytoprotective and Anti-tumor Activities of Isatin Schiff Bases".LETTERS IN DRUG DESIGN & DISCOVERY 12.10(2015):802-805.

入库方式: OAI收割

来源:昆明植物研究所

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