Structure–activity relationship in the oxazolidinone–quinolone hybrid series: influence of the central spacer on the antibacterial activity and the mode of action

Bioorganic & Medicinal Chemistry Letters
2003.0

Abstract

Oxazolidinone-quinolone hybrids, which combine the pharmacophores of a quinolone and an oxazolidinone, were synthesised and shown to be active against a variety of susceptible and resistant Gram-positive and Gram-negative bacteria. The nature of the spacer greatly influences the antibacterial activity by directing the mode of action, that is quinolone- and/or oxazolidinone-like activity. The best compounds in this series have a balanced dual mode of action and overcome all types of resistance, including resistance to quinolones and linezolid, in clinically relevant Gram-positive pathogens.

Knowledge Graph

Similar Paper

Structure–activity relationship in the oxazolidinone–quinolone hybrid series: influence of the central spacer on the antibacterial activity and the mode of action
Bioorganic & Medicinal Chemistry Letters 2003.0
Novel oxazolidinone–quinolone hybrid antimicrobials
Bioorganic & Medicinal Chemistry Letters 2003.0
Design, Synthesis, and Evaluation of Novel Fluoroquinolone−Aminoglycoside Hybrid Antibiotics
Journal of Medicinal Chemistry 2009.0
Synthesis and antibacterial activities of novel oxazolidinones having spiro[2,4]heptane moieties
Bioorganic & Medicinal Chemistry Letters 2009.0
4-Quinolone hybrids and their antibacterial activities
European Journal of Medicinal Chemistry 2017.0
The effect of remote chirality on the antibacterial activity of indolinyl, tetrahydroquinolyl and dihydrobenzoxazinyl oxazolidinones
Bioorganic & Medicinal Chemistry Letters 2003.0
Design, synthesis and structure-activity relationships of novel 15-membered macrolides: Quinolone/quinoline-containing sidechains tethered to the C-6 position of azithromycin acylides
European Journal of Medicinal Chemistry 2020.0
Synthesis, SAR and antibacterial studies on novel chalcone oxazolidinone hybrids
European Journal of Medicinal Chemistry 2007.0
The synthesis and biological evaluation of a novel series of antimicrobials of the oxazolidinone class
Bioorganic & Medicinal Chemistry Letters 2002.0
1,2,4-Triazole-quinoline/quinolone hybrids as potential anti-bacterial agents
European Journal of Medicinal Chemistry 2019.0