Synthesis and antibacterial activity of 6-O-(heteroaryl-isoxazolyl)propynyl 2-fluoro ketolides

Bioorganic & Medicinal Chemistry Letters
2012.0

Abstract

Macrolide antibiotics are widely prescribed for the treatment of respiratory tract infections; however, the increasing prevalence of macrolide-resistant pathogens is a public health concern. Therefore, the development of new macrolide derivatives with activities against resistant pathogens is urgently needed. A series of novel 6-O-(heteroaryl-isoxazolyl)propynyl 2-fluoro ketolides has been synthesized from erythromycin A. These compounds have shown very promising in vitro and in vivo antibacterial activities against key respiratory pathogens including erythromycin-susceptible/resistant strains.

Knowledge Graph

Similar Paper

Synthesis and antibacterial activity of 6-O-(heteroaryl-isoxazolyl)propynyl 2-fluoro ketolides
Bioorganic & Medicinal Chemistry Letters 2012.0
Synthesis and Antibacterial Activity of 6-O-Arylbutynyl Ketolides with Improved Activity against Some Key Erythromycin-Resistant Pathogens
Journal of Medicinal Chemistry 2003.0
Synthesis and antibacterial activity of 6-O-heteroarylcarbamoyl-11,12-lactoketolides
Bioorganic & Medicinal Chemistry Letters 2006.0
Synthesis and Antibacterial Activity of Ketolides (6-O-Methyl-3-oxoerythromycin Derivatives):  A New Class of Antibacterials Highly Potent Against Macrolide-Resistant and -Susceptible Respiratory Pathogens
Journal of Medicinal Chemistry 1998.0
Synthesis and antibacterial activity of 6-O-arylpropargyl-9-oxime-11,12-carbamate ketolides
Bioorganic & Medicinal Chemistry Letters 2004.0
Synthesis and antibacterial activity of novel 2‑fluoro ketolide antibiotics with 11,12‑quinoylalkyl side chains
Bioorganic & Medicinal Chemistry Letters 2023.0
Synthesis and antibacterial activity of novel 6 -O- substituted erythromycin A derivatives
Bioorganic & Medicinal Chemistry Letters 2000.0
Novel Erythromycin Derivatives with Aryl Groups Tethered to the C-6 Position Are Potent Protein Synthesis Inhibitors and Active against Multidrug-Resistant Respiratory Pathogens
Journal of Medicinal Chemistry 2001.0
Synthesis and structure–activity relationship of a novel class of 15-membered macrolide antibiotics known as ‘11a-azalides’
Bioorganic & Medicinal Chemistry 2012.0
Synthesis of 3,6-bicyclolides: A novel class of macrolide antibiotics
Bioorganic & Medicinal Chemistry Letters 2008.0