Conformations in solution and bound to bacterial ribosomes of ketolides, HMR 3647 (telithromycin) and RU 72366: A new class of highly potent antibacterials

Author:

Evrard-Todeschi Nathalie,Gharbi-Benarous Josyane,Gaillet Christine,Verdier Laurent,Bertho Gildas,Lang Catherine,Parent Annick,Girault Jean-Pierre

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference53 articles.

1. Synthesis and antibacterial activity of HMR 3647 a new ketolide highly potent against erythromycin-resistant and susceptible pathogens

2. Decomposition kinetics of erythromycin A in acidic aqueous solutions

3. Agouridas, C.; Collette, P.; Mauvais, P.; Chantot, J. F. 34th Interscience Conference on Antimicrobial Agents and Chemotherapy, 1994; F-166.

4. Agouridas, C.; Benedetti, Y.; Denis, A.; Le Martret, O.; Chantot, J. F. 35th Interscience Conference on Antimicrobial Agents and Chemotherapy, 1995; F-157.

5. 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

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