Khanna Aanchal, Kumar Nitish, Rana Rupali, Sharma Anchal, Kaur Harmandeep, Bedi Preet Mohinder Singh
Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab 143005, India.
Sri Sai College of Pharmacy, Badhani, Pathankot, Punjab 145001, India.
Bioorg Chem. 2024 Dec;153:107773. doi: 10.1016/j.bioorg.2024.107773. Epub 2024 Sep 2.
Antimicrobial resistance poses a global health concern and develops a need to discover novel antimicrobial agents or targets to tackle this problem. Fluoroquinolone (FN), a DNA gyrase and topoisomerase IV inhibitor, has helped to conquer antimicrobial resistance as it provides flexibility to researchers to rationally modify its structure to increase potency and efficacy. This review provides insights into the rational modification of FNs, the causes of resistance to FNs, and the mechanism of action of FNs. Herein, we have explored the latest advancements in antimicrobial activities of FN analogues and the effect of various substitutions with a focus on utilizing the FN nucleus to search for novel potential antimicrobial candidates. Moreover, this review also provides a comparative analysis of two widely prescribed FNs that are ciprofloxacin and norfloxacin, explaining their rationale for their design, structure-activity relationships (SAR), causes of resistance, and mechanistic studies. These insights will prove advantageous for new researchers by aiding them in designing novel and effective FN-based compounds to combat antimicrobial resistance.
抗菌药物耐药性引起了全球健康关注,并产生了发现新型抗菌剂或靶点以解决这一问题的需求。氟喹诺酮(FN)是一种DNA旋转酶和拓扑异构酶IV抑制剂,它为研究人员合理修饰其结构以提高效力和疗效提供了灵活性,有助于攻克抗菌药物耐药性。本综述深入探讨了氟喹诺酮类药物的合理修饰、对氟喹诺酮类药物耐药的原因以及氟喹诺酮类药物的作用机制。在此,我们探索了氟喹诺酮类似物抗菌活性的最新进展以及各种取代基的影响,重点是利用氟喹诺酮核心结构寻找新型潜在抗菌候选物。此外,本综述还对两种广泛使用的氟喹诺酮类药物环丙沙星和诺氟沙星进行了比较分析,解释了它们的设计原理、构效关系(SAR)、耐药原因和作用机制研究。这些见解将有助于新研究人员设计新型有效的基于氟喹诺酮的化合物来对抗抗菌药物耐药性,对他们具有重要意义。