Ontology highlight
ABSTRACT:
SUBMITTER: Hu XL
PROVIDER: S-EPMC4499819 | biostudies-other | 2015 Jul
REPOSITORIES: biostudies-other
ACS medicinal chemistry letters 20150601 7
We show here that a series of triazolyl glycolipid derivatives modularly synthesized by a "click" reaction have the ability to increase the susceptibility of a drug-resistant bacterium to β-lactam antibiotics. We determine that the glycolipids can suppress the minimal inhibitory concentration of a number of ineffective β-lactams, upward of 256-fold, for methicillin-resistant Staphylococuss aureus (MRSA). The mechanism of action has been preliminarily probed and discussed. ...[more]