| Literature DB >> 24470840 |
Bharat Wagh1, Tapas Paul1, Charles Debrosse1, Dorota Klepacki2, Meagan C Small3, Alexander D Mackerell3, Rodrigo B Andrade1.
Abstract
Antibiotic-resistant bacteria are emerging at an alarming rate in both hospital and community settings. Motivated by this issue, we have prepared desmethyl (i.e., replacing methyl groups with hydrogens) analogues of third-generation macrolide drugs telithromycin (TEL, 2) and cethromycin (CET, 6), both of which are semi-synthetic derivatives of flagship macrolide antibiotic erythromycin (1). Herein, we report the total synthesis, molecular modeling, and biological evaluation of 4,8,10-tridesmethyl cethromycin (7). In MIC assays, CET analogue 7 was found to be equipotent with TEL (2) against a wild-type E. coli strain, more potent than previously disclosed desmethyl TEL congeners 3, 4, and 5, but fourfold less potent than TEL (2) against a mutant E. coli A2058G strain.Entities:
Keywords: antibiotic resistance; cethromycin; desmethyl analogues; ketolide antibiotics; molecular modeling; telithromycin; total synthesis
Year: 2013 PMID: 24470840 PMCID: PMC3901159 DOI: 10.1021/ml400337t
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345