Halogens in Protein-Ligand Binding Mechanism: A Structural Perspective

被引:115
|
作者
Shinada, Nicolas K. [1 ,2 ,3 ,4 ]
de Brevern, Alexandre G. [2 ,3 ,4 ]
Schmidtke, Peter [1 ]
机构
[1] Discngine SAS, 79 Ave Ledru Rollin, F-75012 Paris, France
[2] Univ Antilles, Univ Paris Diderot, Sorbonne Paris Cite,INSERM, Univ Reunion,UMR S1134,Biol Integree Globule Roug, F-75739 Paris, France
[3] Lab Excellence GR Ex, F-75739 Paris, France
[4] INTS, F-75739 Paris, France
关键词
ORTHOGONAL MULTIPOLAR INTERACTIONS; HYDROGEN-BONDS; MEDICINAL CHEMISTRY; FLUORINE-ATOMS; SULFUR-ATOMS; RECOGNITION; INHIBITORS; GEOMETRY; DATABASE; DESIGN;
D O I
10.1021/acs.jmedchem.8b01453
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Halogen atoms have been at the center of many rational medicinal chemistry applications in drug design. While fluorine and chlorine atoms are often added to enhance physicochemical properties, bromine and iodine elements are generally inserted to improve selectivity. Favorable halogen interactions such as halogen bond have been thoroughly studied through quantum mechanics and statistical analyses. Although most of the studies focus on halogen interaction through its a-hole, hydrogen bonding also has a significant impact. Here, we present an analysis describing the interacting environment of halogen atoms in protein ligand context. With consideration of structural redundancy in the PDB, tendencies toward specific molecular interactions consideration have been refined and implications for rational drug design with halogens further discussed. Finally, we highlight the moderate occurrence of halogen bonding and present the other roles of halogen in protein-ligand complexes, completing the medicinal chemistry guide to rational halogen interactions.
引用
收藏
页码:9341 / 9356
页数:16
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