| Literature DB >> 25050164 |
Vinayak S Khodade1, Mallojjala Sharath Chandra1, Ankita Banerjee2, Surobhi Lahiri2, Mallikarjuna Pulipeta2, Radha Rangarajan2, Harinath Chakrapani1.
Abstract
The number of cases of drug resistant Staphylococcus aureus infections is on the rise globally and new strategies to identify drug candidates with novel mechanisms of action are in urgent need. Here, we report the synthesis and evaluation of a series of benzo[b]phenanthridine-5,7,12(6H)-triones, which were designed based on redox-active natural products. We find that the in vitro inhibitory activity of 6-(prop-2-ynyl)benzo[b]phenanthridine-5,7,12(6H)-trione (1f) against methicillin-resistant Staphylococcus aureus (MRSA), including a panel of patient-derived strains, is comparable or better than vancomycin. We show that the lead compound generates reactive oxygen species (ROS) in the cell, contributing to its antibacterial activity.Entities:
Keywords: DNA damage; Drug resistance; MRSA; RecA; reactive oxygen species; superoxide radical
Year: 2014 PMID: 25050164 PMCID: PMC4094247 DOI: 10.1021/ml5001118
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345