An overview of recent progress in siderophore-antibiotic conjugates

European Journal of Medicinal Chemistry
2019.0

Abstract

Multi-drug resistant infections caused by Gram-negative bacteria have become one of the most important reasons for the failure of clinical anti-infective treatment. Siderophore-antibiotic conjugates, which were designed based on a "Trojan horse" strategy wherein features enabled active uptake to bypass the Gram-negative cell wall, have been expected to be a weapon for anti-infective treatment in the clinic. Herein, we review antibiotic drug design strategies based on mimics of nature siderophores reported in recent years, we also focus our attention on the relationship between the type of linker and the corresponding antibacterial activity.

Knowledge Graph

Similar Paper

An overview of recent progress in siderophore-antibiotic conjugates
European Journal of Medicinal Chemistry 2019.0
Targeted Antibiotic Delivery: Selective Siderophore Conjugation with Daptomycin Confers Potent Activity against Multidrug Resistant Acinetobacter baumannii Both in Vitro and in Vivo
Journal of Medicinal Chemistry 2017.0
Synthesis and antibacterial activity of catecholate–ciprofloxacin conjugates
Bioorganic & Medicinal Chemistry 2014.0
Siderophores: Chemical tools for precise antibiotic delivery
Bioorganic & Medicinal Chemistry Letters 2023.0
Novel monobactams utilizing a siderophore uptake mechanism for the treatment of gram-negative infections
Bioorganic & Medicinal Chemistry Letters 2012.0
Design, synthesis and biological evaluation of monobactams as antibacterial agents against gram-negative bacteria
European Journal of Medicinal Chemistry 2016.0
Siderophore Receptor-Mediated Uptake of Lactivicin Analogues in Gram-Negative Bacteria
Journal of Medicinal Chemistry 2014.0
Discovery of Novel Pyridone-Conjugated Monosulfactams as Potent and Broad-Spectrum Antibiotics for Multidrug-Resistant Gram-Negative Infections
Journal of Medicinal Chemistry 2017.0
Chemical syntheses and in vitro antibacterial activity of two desferrioxamine B-ciprofloxacin conjugates with potential esterase and phosphatase triggered drug release linkers
Bioorganic & Medicinal Chemistry 2012.0
Highly Antibacterial Active Aminoacyl Penicillin Conjugates with Acylated Bis-Catecholate Siderophores Based on Secondary Diamino Acids and Related Compounds
Journal of Medicinal Chemistry 2002.0