Alastair L Parkes, Oliver A Bardell-Cox, Ricky M Cain
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The state of the art in dual-acting hybrid antibiotics to combat bacterial resistance.
Introduction: The efficacy of current treatments for bacterial infections is under threat due to the continuing rise in the prevalence of antimicrobial resistance (AMR). Resistance can arise due to a wide variety of changes in the bacterial cell that prevent the antibiotic from acting on its target. This can be through changes to the target itself or changes that limit access to the target. Strategies to overcome resistance therefore either seek to reestablish access to the target or to engage a different target for which resistance is yet to arise. This has been done successfully in the clinic through co-dosing of more than one molecule, but a long-held aim has been to achieve efficacy in a single 'hybrid' molecule.
Areas covered: The authors review the progress since 2016 of hybrid antibiotics in clinical trials, cover some advances in preclinical research into dual-acting hybrids, and examine alternative approaches to using bi-functional hybrid molecules to tackle AMR.
Expert opinion: Many contributory factors, both scientific and economic, have limited the success of dual-acting hybrids where both partners are antibiotics. The success of cefiderocol highlights the potential of linking molecules that target bacteria directly and non-antibiotics. These strategies offer some exciting possibilities.
期刊介绍:
Expert Opinion on Drug Discovery (ISSN 1746-0441 [print], 1746-045X [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on novel technologies involved in the drug discovery process, leading to new leads and reduced attrition rates. Each article is structured to incorporate the author’s own expert opinion on the scope for future development.
The Editors welcome:
Reviews covering chemoinformatics; bioinformatics; assay development; novel screening technologies; in vitro/in vivo models; structure-based drug design; systems biology
Drug Case Histories examining the steps involved in the preclinical and clinical development of a particular drug
The audience consists of scientists and managers in the healthcare and pharmaceutical industry, academic pharmaceutical scientists and other closely related professionals looking to enhance the success of their drug candidates through optimisation at the preclinical level.