Design and synthesis of imidazo[4,5-c]pyridine derivatives as promising Aurora kinase A (AURKA) inhibitors


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

Computer simulation at the PM7 level of theory of the structures of imidazo[4,5-c]pyridine derivatives (deaza analogs of purines) and their complexes with Aurora kinase A (AURKA) indicated prospects for their use as potential AURKA inhibitors in the treatment of oncological diseases. A number of new compounds of the selected imidazo[4,5-c]pyridine series, for which the highest inhibitory activity against AURKA was predicted, were synthesized in high yields for further biological testing.

作者简介

D. Lomov

Litvinenko Institute of Physical Organic Chemistry

编辑信件的主要联系方式.
Email: lomov_dmitrii@mail.ru
乌克兰, ul. Rozy Lyuksemburg 70, Donetsk, 83000

S. Lyashchuk

Litvinenko Institute of Physical Organic Chemistry

Email: lomov_dmitrii@mail.ru
乌克兰, ul. Rozy Lyuksemburg 70, Donetsk, 83000

M. Abramyants

Litvinenko Institute of Physical Organic Chemistry

Email: lomov_dmitrii@mail.ru
乌克兰, ul. Rozy Lyuksemburg 70, Donetsk, 83000

补充文件

附件文件
动作
1. JATS XML

版权所有 © Pleiades Publishing, Ltd., 2016