Tuning the Antibacterial Activity of Amphiphilic Neamine Derivatives and Comparison to Paromamine Homologues-Reference-Cited by-同舟云学术

Tuning the Antibacterial Activity of Amphiphilic Neamine Derivatives and Comparison to Paromamine Homologues

Published:2013-10-01 Issue:19 Volume:56 Page:7691-7705
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Zimmermann Louis¹,Bussière Antoine¹,Ouberai Myriam²,Baussanne Isabelle¹,Jolivalt Claude³,Mingeot-Leclercq Marie-Paule²,Décout Jean-Luc¹

Affiliation:

1. Département de Pharmacochimie Moléculaire, Université de Grenoble I/CNRS, UMR 5063, ICMG FR 2607, 470 rue de la Chimie, BP 53, F-38041 Grenoble, France

2. Unité de Pharmacologie Cellulaire et Moléculaire, Louvain Drug Research Institute, Université Catholique de Louvain, Avenue E. Mounier 73, B1.73.05, B-1200 Brussels, Belgium

3. Ecole Nationale de Chimie de Paris/CNRS, UMR 7573, 11 rue Pierre et Marie Curie, F-75231 Paris cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm401148j

Reference88 articles.

1. Interaction of antibiotics with functional sites in 16S ribosomal RNA

2. Interactions of a small RNA with antibiotic and RNA ligands of the 30S subunit

3. RNA Sequence Determinants for Aminoglycoside Binding to an A-site rRNA Model Oligonucleotide

4. Binding of neomycin-class aminoglycoside antibiotics to the A-site of 16 s rRNA

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