Suppr超能文献

新型 4-苯胺基喹唑啉衍生物的合成、抗肿瘤评价及对接研究,作为潜在的表皮生长因子受体(EGFR)抑制剂。

Synthesis, antitumor evaluation and docking study of novel 4-anilinoquinazoline derivatives as potential epidermal growth factor receptor (EGFR) inhibitors.

机构信息

College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, PR China.

出版信息

ChemMedChem. 2013 Jun;8(6):928-33. doi: 10.1002/cmdc.201300120. Epub 2013 May 2.

Abstract

Strike a pose! A series of 4-anilinoquinazolines were designed, synthesized and evaluated in vitro against lung and breast cancer cell lines. Several compounds were found to be endowed with cytotoxicity in the low micromolar range. Molecular docking suggests that these compounds bind to EGFR in a similar manner to known EGFR inhibitors.

摘要

摆个姿势!设计、合成了一系列 4-苯胺基喹唑啉,并在体外对肺癌和乳腺癌细胞系进行了评估。发现几种化合物具有低微摩尔范围内的细胞毒性。分子对接表明,这些化合物以与已知的 EGFR 抑制剂相似的方式与 EGFR 结合。

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