Imidazopyridine, a promising scaffold with potential medicinal applications and structural activity relationship (SAR): recent advances

被引:37
作者
Khatun, Samima [1 ]
Singh, Abhinav [1 ]
Bader, Ghulam N. [2 ]
Sofi, Firdoos Ahmad [2 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Med Chem, Sahibzada Ajit Singh Nag, Punjab, India
[2] Univ Kashmir, Sch Appl Sci & Technol, Dept Pharmaceut Sci, Srinagar, J&K, India
关键词
Biological activity; imidazopyridine; leads; molecular modeling; structural activity relationship; II RECEPTOR ANTAGONISTS; ACTIVITY IN-VITRO; BIOLOGICAL EVALUATION; ANTIPROLIFERATIVE ACTIVITY; KINASE INHIBITOR; REVERSIBLE INHIBITORS; PYRIDINE-DERIVATIVES; ANTICOCCIDIAL AGENTS; SELECTIVE INHIBITORS; FUNGICIDAL ACTIVITY;
D O I
10.1080/07391102.2021.1997818
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
Imidazopyridine scaffold has gained tremendous importance over the past few decades. Imidazopyridines have been expeditiously used for the rationale design and development of novel synthetic analogs for various therapeutic disorders. A wide variety of imidazopyridine derivatives have been developed as potential anti-cancer, anti-diabetic, anti-tubercular, anti-microbial, anti-viral, antiinflammatory, central nervous system (CNS) agents besides other chemotherapeutic agents. Imidazopyridine heterocyclic system acts as a key pharmacophore motif for the identification and optimization of lead structures to increase medicinal chemistry toolbox. The present review highlights the medicinal significances of imidazopyridines for their rationale development as lead molecules with improved therapeutic efficacies. This review further emphasis on the structure-activity relationships (SARs) of the various designed imidazopyridines to establish a relationship between the key structural features versus the biological activities.
引用
收藏
页码:14279 / 14302
页数:24
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