A Critical Review on Therapeutic Potential of Benzimidazole Derivatives: A Privileged Scaffold

被引:1
|
作者
Natarajan, Ramalakshmi [1 ]
Kumar, Padma [1 ]
Subramani, Arunkumar [2 ]
Siraperuman, Amuthalakshmi [1 ]
Angamuthu, Prabakaran [1 ]
Bhandare, Richie R. [3 ]
Shaik, Afzal B. [4 ,5 ]
机构
[1] Dr MGR Med Univ, Dept Pharmaceut Chem, CL Baid Metha Coll Pharm, Chennai 600097, Tamil Nadu, India
[2] Sathyabama Inst Sci & Technol, Sch Pharm, Dept Pharmaceut Sci, Chennai, India
[3] Ajman Univ, Coll Pharm & Hlth Sci, Dept Pharmaceut Sci, POB 346, Ajman, U Arab Emirates
[4] Jawaharlal Nehru Technol Univ Kakinada, St Marys Grp Inst Guntur, St Marys Coll Pharm, Guntur 522212, Andhra Pradesh, India
[5] Saveetha Inst Med & Tech Sci, Ctr Global Hlth Res, Saveetha Med Coll, Chennai, India
关键词
Benzimidazole; privileged scaffold; structure-activity relationship; multiple targets; lead compounds; SAR; BIOLOGICAL EVALUATION; MOLECULAR DOCKING; ANTIMYCOBACTERIAL ACTIVITY; CRYSTAL-STRUCTURES; DUAL INHIBITORS; DESIGN; AGENTS; DISCOVERY; DNA; BENZOTHIAZOLE;
D O I
10.2174/0115734064253813231025093707
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Benzimidazole nucleus is a predominant heterocycle displaying a wide spectrum of pharmacological activities. The privileged nature of the benzimidazole scaffold has been revealed by its presence in most small molecule drugs and in its ability to bind multiple receptors with high affinity. A literature review of the scaffold reveals several instances where structural modifications of the benzimidazole core have resulted in high-affinity lead compounds against a variety of biological targets. Hence, this structural moiety offers opportunities to discover novel, better, safe and highly potent biological agents. The goal of the present review is to compile the medicinal properties of benzimidazole derivatives with a focus on SAR (Structure-Activity Relationships).
引用
收藏
页码:311 / 351
页数:41
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