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新型黄酮类化合物作为H R抑制剂的设计、合成、生物学评价及分子对接

Design, synthesis, biological evaluation, and molecular docking of novel flavones as H R inhibitors.

作者信息

Wen Gang, Liu Qian, Hu Huabin, Wang Dongmei, Wu Song

机构信息

State Key Laboratory of Bioactive Substances and Functions of Natural Medicines & Ministry of Health Key Laboratory of Biosynthesis of Natural Products, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

出版信息

Chem Biol Drug Des. 2017 Oct;90(4):580-589. doi: 10.1111/cbdd.12981. Epub 2017 Apr 17.

Abstract

A series of novel flavone derivatives were designed, synthesized, and evaluated for their H R inhibitory activity. The results showed that four compounds exhibited significant anti-H R activity. Molecular docking experiments indicated that a salt bridge, hydrogen-bonding, and hydrophobic interactions all contributed to interactions between inhibitors and H R.

摘要

设计、合成了一系列新型黄酮衍生物,并对其HR抑制活性进行了评估。结果表明,四种化合物表现出显著的抗HR活性。分子对接实验表明,盐桥、氢键和疏水相互作用均有助于抑制剂与HR之间的相互作用。

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