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Structure-based design, synthesis and A-site rRNA co-crystal complexes of novel amphiphilic aminoglycoside antibiotics with new binding modes: a synergistic hydrophobic effect against resistant bacteria
Authors:Hanessian Stephen  Pachamuthu Kandasamy  Szychowski Janek  Giguère Alexandre  Swayze Eric E  Migawa Michael T  François Boris  Kondo Jiro  Westhof Eric
Affiliation:Department of Chemistry, Université de Montréal, Montréal, Canada. stephen.hanessian@umontreal.ca
Abstract:Incorporation of an hydrophobic (phenethylamino)ethyl ether at C2″ of N1-(HABA)-3',4'-dideoxyparomomycin led to a novel analog with an excellent antibacterial profile against a host of resistant bacteria.
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