Monocyclic and Fused Azines and Azoles as Histamine H4 Receptor Ligands

被引:4
作者
Lazewska, Dorota [1 ]
Dominguez-Alvarez, Enrique [1 ]
Kaminska, Katarzyna [1 ]
Kuder, Kamil [1 ]
Kiec-Kononowicz, Katarzyna [1 ]
机构
[1] Jagiellonian Univ, Coll Med, Dept Technol & Biotechnol Drugs, Ul Med 9, PL-30688 Krakow, Poland
关键词
Histamine H-4 receptor; GPCR; indolecarboxamides; benzimidazoles; azines; histamine; CONFORMATIONAL RESTRICTION STRATEGY; PROTEIN-COUPLED RECEPTORS; PHARMACOLOGICAL CHARACTERIZATION; MOLECULAR DETERMINANTS; HUMAN EOSINOPHILS; CHOROIDAL NEOVASCULARIZATION; CONSTITUTIVE ACTIVITY; CRYSTAL-STRUCTURE; ALKYL IMIDAZOLES; HIGHLY POTENT;
D O I
10.2174/0929867323666160411143151
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 histamine H-4 receptor has stood out since its discovery and identification in 2000 as an important target in the search for potential new drugs for the treatment of inflammatory and allergic diseases such as rhinitis, pruritus and asthma. Thus, in the last decade, both industry and academia have performed an intensive and productive search for new ligands of this newest subtype of histamine receptor. The most promising compounds found include monocyclic and fused azines, and azoles such as bispyrimidines, di- and triaminopyrimidines, quinazolines, imidazoles, indoles, benzimidazoles and benzazoles. The aim of this review is to give an insight into the current state of the art in the field of histamine H-4 receptor research, focusing mainly on the last five years.
引用
收藏
页码:1870 / 1925
页数:56
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