Synthesis of novel macrolide derivatives with imidazo[4,5-b]pyridinyl sulfur contained alkyl side chains and their antibacterial activity.

Abstract:

:In an effort to find new antibiotics, a novel series of 14-membered macrolides with imidazo[4,5-b]pyridinyl sulfur contained alkyl side chains has been synthesized based on commercially available clarithromycin. Chemical transformation of hydroxy group at position C-3 afforded range of ketolides and acylides. Compared to telithromycin, compound 15a demonstrated improved in vitro activity against erythromycin-susceptible and -resistant strains.

journal_name

Bioorg Med Chem Lett

authors

Xu P,Liu L,Chen XZ,Li Y,Liu J,Jin ZP,Wang GQ,Lei PS

doi

10.1016/j.bmcl.2009.06.023

subject

Has Abstract

pub_date

2009-08-01 00:00:00

pages

4079-83

issue

15

eissn

0960-894X

issn

1464-3405

pii

S0960-894X(09)00842-7

journal_volume

19

pub_type

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