Probing linker design in citric acid–ciprofloxacin conjugates
- 1 August 2014
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 22 (16) , 4499-4505
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Trihydroxamate Siderophore–Fluoroquinolone Conjugates Are Selective Sideromycin Antibiotics that Target Staphylococcus aureusBioconjugate Chemistry, 2013
- Siderophore conjugatesAnnals of the New York Academy of Sciences, 2013
- Synthesis and antibacterial activity of conjugates between norfloxacin and analogues of the siderophore vanchrobactinBioorganic & Medicinal Chemistry, 2013
- Siderophore-Mediated Cargo Delivery to the Cytoplasm of Escherichia coli and Pseudomonas aeruginosa: Syntheses of Monofunctionalized Enterobactin Scaffolds and Evaluation of Enterobactin–Cargo Conjugate UptakeJournal of the American Chemical Society, 2012
- Syntheses of Siderophore–Drug Conjugates Using a Convergent Thiol–Maleimide SystemACS Medicinal Chemistry Letters, 2012
- Chemical syntheses and in vitro antibacterial activity of two desferrioxamine B-ciprofloxacin conjugates with potential esterase and phosphatase triggered drug release linkersBioorganic & Medicinal Chemistry, 2012
- Chemistry and biology of siderophoresNatural Product Reports, 2010
- Is drug release necessary for antimicrobial activity of siderophore-drug conjugates? Syntheses and biological studies of the naturally occurring salmycin “Trojan Horse” antibiotics and synthetic desferridanoxamine-antibiotic conjugatesBioMetals, 2009
- Siderophore-Based Iron Acquisition and Pathogen ControlMicrobiology and Molecular Biology Reviews, 2007
- Studies and Syntheses of Siderophores, Microbial Iron Chelators, and Analogs as Potential Drug Delivery AgentsCurrent Medicinal Chemistry, 2000