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尼洛替尼衍生物的设计、合成及抗肿瘤活性研究。

Design, synthesis and biological activities of Nilotinib derivates as antitumor agents.

机构信息

School of Medicine, Xi'an Jiaotong University, No. 76, Yanta West Road, Xi'an, Shaanxi Province 710061, PR China.

出版信息

Bioorg Med Chem. 2013 May 1;21(9):2527-34. doi: 10.1016/j.bmc.2013.02.036. Epub 2013 Mar 5.

Abstract

A novel class of Nilotinib derivatives, B1-B20, were synthesized in high yields using various substituted anilines. All the title compounds were evaluated for their inhibitory activities against Bcr-Abl and antiproliferative effects on human leukemia cell (K562). The pharmacological results indicated that some compounds exhibited promising anticancer activity. In particular, compound B14 containing tertiary amine side chain exhibited Bcr-Abl inhibitory activity similar to that of Nilotinib. It was suggested that the introduction of the tertiary amine moiety could improve Bcr-Abl inhibitory activity and antitumor effects.

摘要

新型尼洛替尼衍生物 B1-B20 是使用各种取代苯胺高产合成的。所有标题化合物均对 Bcr-Abl 的抑制活性和对人白血病细胞(K562)的增殖抑制作用进行了评估。药理结果表明,一些化合物表现出有希望的抗癌活性。特别是,含有叔胺侧链的化合物 B14 表现出与尼洛替尼相似的 Bcr-Abl 抑制活性。这表明引入叔胺部分可以提高 Bcr-Abl 抑制活性和抗肿瘤作用。

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