Suppr超能文献

合成及一些噻唑并苯并咪唑衍生物的体外细胞毒性评价。

Synthesis and in vitro cytotoxic evaluation of some thiazolylbenzimidazole derivatives.

机构信息

Department of Chemistry, East China Normal University, 3663 North Zhongshan Road, Shanghai 200062, China.

出版信息

Eur J Med Chem. 2011 Jan;46(1):417-22. doi: 10.1016/j.ejmech.2010.11.014. Epub 2010 Nov 27.

Abstract

A novel kind of thiazolylbenzimidazole derivatives were designed and synthesized and evaluated for their antitumor activity against SMMC-7721 and A549 cell lines. Most compounds showed good antitumor activities, and compound 11b displayed remarkable in vitro anticancer activity comparable to taxol. The preliminary structure-activity relationship of these benzimidazole derivatives was discussed based on the experimental data obtained.

摘要

设计并合成了一种新型噻唑并苯并咪唑衍生物,并评价了它们对 SMMC-7721 和 A549 细胞系的抗肿瘤活性。大多数化合物表现出良好的抗肿瘤活性,化合物 11b 表现出与紫杉醇相当的显著体外抗癌活性。根据获得的实验数据,讨论了这些苯并咪唑衍生物的初步构效关系。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验