亲脂性
氟
化学
配体(生物化学)
配体效率
组合化学
代谢稳定性
有机化学
计算化学
生物化学
受体
体外
作者
Hans‐Joachim Böhm,David W. Banner,Stefanie Bendels,Manfred Kansy,Bernd Kuhn,Klaus Müller,U. Obst-Sander,Martin Ståhl
出处
期刊:ChemBioChem
[Wiley]
日期:2004-04-28
卷期号:5 (5): 637-643
被引量:1410
标识
DOI:10.1002/cbic.200301023
摘要
Abstract Fluorinated compounds are synthesized in pharmaceutical research on a routine basis and many marketed compounds contain fluorine. The present review summarizes some of the most frequently employed strategies for using fluorine substituents in medicinal chemistry. Quite often, fluorine is introduced to improve the metabolic stability by blocking metabolically labile sites. However, fluorine can also be used to modulate the physicochemical properties, such as lipophilicity or basicity. It may exert a substantial effect on the conformation of a molecule. Increasingly, fluorine is used to enhance the binding affinity to the target protein. Recent 3D‐structure determinations of protein complexes with bound fluorinated ligands have led to an improved understanding of the nonbonding protein–ligand interactions that involve fluorine.
科研通智能强力驱动
Strongly Powered by AbleSci AI