Molecular Modeling of Histamine Receptors-Recent Advances in Drug Discovery

被引:18
|
作者
Mehta, Pakhuri [1 ]
Miszta, Przemyslaw [1 ]
Filipek, Slawomir [1 ]
机构
[1] Univ Warsaw, Fac Chem, Biol & Chem Res Ctr, PL-02093 Warsaw, Poland
来源
MOLECULES | 2021年 / 26卷 / 06期
关键词
histamine receptors; G protein-coupled receptors; computational studies; molecular docking; virtual screening; drug discovery and design; PROTEIN-COUPLED RECEPTORS; H-4; RECEPTOR; BIOLOGICAL EVALUATION; H4; CRYSTAL-STRUCTURE; IN-SILICO; PHARMACOLOGICAL CHARACTERIZATION; ANTAGONISTS/INVERSE AGONISTS; THERAPEUTIC TARGET; LIGAND-BINDING;
D O I
10.3390/molecules26061778
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The recent developments of fast reliable docking, virtual screening and other algorithms gave rise to discovery of many novel ligands of histamine receptors that could be used for treatment of allergic inflammatory disorders, central nervous system pathologies, pain, cancer and obesity. Furthermore, the pharmacological profiles of ligands clearly indicate that these receptors may be considered as targets not only for selective but also for multi-target drugs that could be used for treatment of complex disorders such as Alzheimer's disease. Therefore, analysis of protein-ligand recognition in the binding site of histamine receptors and also other molecular targets has become a valuable tool in drug design toolkit. This review covers the period 2014-2020 in the field of theoretical investigations of histamine receptors mostly based on molecular modeling as well as the experimental characterization of novel ligands of these receptors.
引用
收藏
页数:25
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