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New Semi-synthetic Glycopeptide Analogs for Combatting Drug-resistant VRE Infections
Rimomycin as a new type V GPA to combat VRE and Mycobacteria strains
Background
Glycopeptide antibiotics (GPAs) are the ‘last-resort’ drugs reserved for the treatment of serious drug-resistant Gram-positive infections. Their beneficial efficacies are exhaustively challenged by the emergence and distribution of GPA-resistant pathogens, vancomycin resistant enterococcus (VRE), in healthcare settings, propelling the innovative discovery/development of more effective GPAs. Type V GPAs provide a unique mode of action that enables them to be very promising lead compounds for drug discovery and development to combat drug-resistant and particularly VRE infections.
Technology Overview
A team of researchers from McMaster has identified a new Type V GPA, rimomycin, that is active against VRE and Mycobacteria strains. After running medicinal chemistry campaigns on rimomycin, a lead compound has been identified that shows 8- and 16- fold decrease
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