1.
J Med Chem
; 47(12): 2965-8, 2004 Jun 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15163176
RESUMO
Novel 4'-substituted 16-membered ring macrolides were synthesized by the cleavage of the mycarose sugar of tylosin and subsequent modification of 4'-hydroxyl group. This new class of macrolide antibiotics exhibited potent activity against some key erythromycin-resistant pathogens.