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发现一类作为口服生物可利用的CDK1/4/6抑制剂的二杂芳胺。

Discovery of a class of diheteroaromatic amines as orally bioavailable CDK1/4/6 inhibitors.

作者信息

Fu Yan, Tang Shuai, Su Yi, Lan Xiaojing, Ye Yan, Zha Chuantao, Li Lei, Cao Jianhua, Chen Yi, Jiang Lei, Huang Ying, Ding Jian, Geng Meiyu, Huang Min, Wan Huixin

机构信息

Shanghai HaiHe Pharmaceutial, Co., Ltd., No. 421 Newton Road, Zhangjiang Hi-tech Park, Pudong New Area, Shanghai 201203, China.

Shanghai Institute of Materia Medica, Chinese Academy of Science, No. 555 Zuchongzhi Road, Zhangjiang Hi-tech Park, Pudong New Area, Shanghai 201203, China.

出版信息

Bioorg Med Chem Lett. 2017 Dec 1;27(23):5332-5336. doi: 10.1016/j.bmcl.2017.09.050. Epub 2017 Oct 16.

Abstract

The discovery of a class of diheteroaromatic amines based on LY2835219 as cyclin-dependent kinase (CDK1/4/6) inhibitors was described. The series was found to have much more improved CDK1 inhibition and potent in vitro anti-proliferative effects against cancer cell lines. The synthesis and structure-activity relationship studies of these compounds were reported. One promising compound was selected to evaluate as a novel lead compound after in vitro and in vivo profiling.

摘要

描述了一类基于LY2835219的二杂芳胺作为细胞周期蛋白依赖性激酶(CDK1/4/6)抑制剂的发现。该系列化合物被发现具有更强的CDK1抑制活性以及对癌细胞系有效的体外抗增殖作用。报道了这些化合物的合成及构效关系研究。在进行体外和体内分析后,选择了一种有前景的化合物作为新型先导化合物进行评估。

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