阿托品
轴手性
手性(物理)
化学
药物发现
立体化学
计算生物学
对映选择合成
生物化学
物理
生物
催化作用
夸克
Nambu–Jona Lasinio模型
手征对称破缺
量子力学
作者
Sean T. Toenjes,Jeffrey L. Gustafson
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2018-01-30
卷期号:10 (4): 409-422
被引量:280
标识
DOI:10.4155/fmc-2017-0152
摘要
Atropisomerism is a dynamic type of axial chirality that is ubiquitous in medicinal chemistry. There are several examples of stable atropisomeric US FDA-approved drugs and experimental compounds, and in each case the atropisomers of these compounds possess drastically different biological activities. Rapidly interconverting atropisomerism is even more prevalent, and while such compounds are typically considered achiral, they bind their protein targets in an atroposelective fashion, with the nonrelevant atropisomer contributing little to the desired activities. It has been recently demonstrated that various properties of an interconverting atropisomer can be modulated through the synthesis of atropisomer stable and pure analogs. Herein we discuss examples of atropisomerism in drug discovery as well as challenges and opportunities moving forward.
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