Affiliations 

  • 1 Faculty of Science and Technology, Quest International University Perak, Ipoh, 30250, Perak, Malaysia
  • 2 Department of Paediatrics, Zhuji Affiliated Hospital of Shaoxing University, Shaoxing, China. Electronic address: zjzjzly1111@163.com
Eur J Med Chem, 2021 Nov 15;224:113741.
PMID: 34365130 DOI: 10.1016/j.ejmech.2021.113741

Abstract

Bacterial infection is amongst the most common diseases in community and hospital settings. Fluoroquinolones, exerting the antibacterial activity through binding to type II bacterial topoisomerase enzymes, DNA gyrase and topoisomerase IV, are mainstays of chemotherapy. At present, fluoroquinolones are the most valuable antibacterial agents used popularly. However, the emergence of more virulent and resistant pathogens by the development of either mutated DNA-binding proteins or efflux pump mechanism for fluoroquinolones results in an urgent demand to develop new fluoroquinolones to withstand the drug resistance and to obtain a broader spectrum of activity. This review aims to outline the recent advances of fluoroquinolone derivatives with antibacterial potential and to summarize the structure-activity relationship (SAR) so as to provide an insight for rational design of more active candidates, covering articles published between January 2018 and June 2021.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.