Because of their various pharmacological actions and structural plasticity, benzimidazoles, a class of heterocyclic molecules, have received much attention in medicinal chemistry. This review paper aims to provide a complete overview of the current developments and future possibilities of benzimidazoles as promising candidates for the creation of innovative therapeutic medicines. The introduction discusses the importance of benzimidazoles in medicinal chemistry, emphasizing their wide range of uses, which include antibacterial, anticancer, and central nervous system actions. The structural properties of benzimidazoles and the effect of substituent changes on their biological activity are investigated, as well as crucial structure-activity relationship (SAR) investigations. The review looks into the synthesis of benzimidazole derivatives, including both traditional and novel methods. The rise of microwave-assisted synthesis, green chemistry methodologies, and solid phase strategies for chemical manufacturing are explored. A thorough review of current breakthroughs in benzimidazole medicinal chemistry emphasizes the importance of target-based drug design, high throughput screening, and computational approaches in expediting drug discovery. As prospective directions for future research, the numerous applications of benzimidazoles in personalized medicine, nanotechnology-assisted medication delivery, and the examination of natural sources for chemical discovery are noted. However, concerns about toxicity, pharmacokinetic limits, and intellectual property difficulties have been raised, leading a cautious assessment of benzimidazole-based therapies. Benzimidazoles, medicinal chemistry, pharmacological activities, synthesis methodologies, structure-activity connection, drug discovery, and future possibilities are some of the keywords used in this study.
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Kumawat et al. (2024) studied this question.
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