De Falco Antonietta, Alfano Antonella Ilenia, Cutarella Luigi, Mori Mattia, Brindisi Margherita
Department of Pharmacy (DoE 2023-2027), University of Naples Federico II, via D. Montesano 49, 80131 Naples, Italy.
Department of Biotechnology, Chemistry, and Pharmacy, University of Siena, via Aldo Moro, 2, 53100 Siena, Italy.
J Med Chem. 2025 Jun 12;68(11):10556-10576. doi: 10.1021/acs.jmedchem.5c00553. Epub 2025 May 30.
The spread of antimicrobial resistance (AMR) represents a major global health challenge, weakening the efficacy of antibiotics such as β-lactams, which are, nowadays, the most widely used drugs for treating bacterial infections. Among the different resistance mechanisms, the production of β-lactamases, particularly metallo-β-lactamases (MBLs), significantly compromises the activity of these antibiotics. Despite progress in developing serine-β-lactamase inhibitors (SBLi), no MBL inhibitors (MBLi) are currently available in clinical practice. This Perspective provides an outlook on AMR mechanisms, with a focus on the expression of MBL enzymes, and showcases the main classes of MBLi proposed to date, which mainly act through coordination of the zinc ion(s) populating the active site of the MBL class of enzymes. Furthermore, the Perspective describes current strategies aimed at overcoming the limited cellular permeability of MBLi, one of the major hurdles preventing their translation into clinical studies.
抗菌药物耐药性(AMR)的传播是一项重大的全球健康挑战,它削弱了β-内酰胺类等抗生素的疗效,而β-内酰胺类抗生素是目前治疗细菌感染最广泛使用的药物。在不同的耐药机制中,β-内酰胺酶的产生,尤其是金属β-内酰胺酶(MBLs),严重损害了这些抗生素的活性。尽管在开发丝氨酸β-内酰胺酶抑制剂(SBLi)方面取得了进展,但目前临床实践中尚无MBL抑制剂(MBLi)。本观点文章对AMR机制进行了展望,重点关注MBL酶的表达,并展示了迄今为止提出的主要MBLi类别,这些抑制剂主要通过与占据MBL类酶活性位点的锌离子配位来发挥作用。此外,该观点文章还描述了目前旨在克服MBLi有限的细胞通透性的策略,这是阻碍它们转化为临床研究的主要障碍之一。