Innovative Medicines Group, Institute of Health & Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove, Qld, 4059, Australia.
Innovative Medicines Group, Institute of Health & Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove, Qld, 4059, Australia.
Eur J Med Chem. 2020 Aug 1;199:112326. doi: 10.1016/j.ejmech.2020.112326. Epub 2020 Apr 28.
Antimicrobial resistance is one of the greatest challenges facing the world today. In the United States alone, it is responsible for the death of more than 20,000 people each year. DNA gyrase, a well-validated drug target, is involved in bacterial DNA replication, repair and decatenation. Currently, the fluoroquinolone class of antibacterials act via inhibition of the DNA gyrase enzyme. However, their efficacy is hindered by the increasing incidence of antimicrobial resistance. Therefore, in this review, we provide an account regarding the structure of DNA gyrase and quinoline and non-quinolone inhibitors published within the last five years (2015-2019). Further, we also discuss molecular interactions and structure-activity relationship studies of the published inhibitors.
抗菌药物耐药性是当今世界面临的最大挑战之一。仅在美国,每年就有超过 20000 人因此死亡。DNA 回旋酶是一个经过充分验证的药物靶点,参与细菌 DNA 的复制、修复和解链。目前,氟喹诺酮类抗菌药物通过抑制 DNA 回旋酶发挥作用。然而,由于抗菌药物耐药性的发生率不断增加,它们的疗效受到了阻碍。因此,在这篇综述中,我们提供了过去五年(2015-2019 年)发表的关于 DNA 回旋酶和喹啉及非喹啉抑制剂的结构和综述。此外,我们还讨论了已发表抑制剂的分子相互作用和构效关系研究。