Document Report Card

ID: ALA1134276

Journal: J Med Chem

Title: Synthesis and antibacterial activity of acylides (3-O-acyl-erythromycin derivatives): a novel class of macrolide antibiotics.

Authors: Tanikawa T, Asaka T, Kashimura M, Misawa Y, Suzuki K, Sato M, Kameo K, Morimoto S, Nishida A.

Abstract: Introduction of an acyl group to the 3-O-position of erythromycin A derivatives instead of L-cladinose led to a novel class of macrolide antibiotics that we named "acylides". The 3-O-nitrophenylacetyl derivative TEA0777 showed significantly potent activity against not only erythromycin-susceptible Gram-positive pathogens but also inducibly macrolides-lincosamides-streptogramin B (MLS(B))-resistant Staphylococcus aureus and efflux-resistant Streptococcus pneumoniae. These results indicated that acylides have potential as next-generation macrolide antibiotics.

CiteXplore: 11708904

DOI: 10.1021/jm015566s