| Literature DB >> 20053481 |
Bohua Long1, Chunlian He, Yingbin Yang, Jiannan Xiang.
Abstract
The synthesis and structure-activity relationships of a series of new penems bearing ferrocenyl group attached to the C-2 position of the penem nucleus were described. The beta-lactanic derivatives obtained had been characterized as sodium salts, through (1)H NMR and IR, as well as through element analysis. Their in vitro antibacterial activities against both Gram-positive including meticillin-resistant Staphylococcus aureus (MRSA) and Gram-negative bacteria were tested. Most of the penems exhibited superior or equivalent efficacy of antibacterial activity as well as high stability to renal dehydropeptidase-I (DHP-I) compared with faropenem. In particular, the compound 14h having a heterocyclic group showed the most potent antibacterial activity. Copyright (c) 2009. Published by Elsevier Masson SAS.Entities:
Mesh:
Substances:
Year: 2009 PMID: 20053481 DOI: 10.1016/j.ejmech.2009.12.045
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514