subject area of
- A combinatorial approach to the discovery of biocidal six-residue cyclic D,L-alpha-peptides against the bacteria methicillin-resistant Staphylococcus aureus (MRSA) and E-coli and the biofouling algae Ulva linza and Navicula perminuta Academic Article
- Combinatorial synthesis through disulfide exchange: Discovery of potent psammaplin a type antibacterial agents active against methicillin-resistant staphylococcus aureus (MRSA) Academic Article
- Design and synthesis via click chemistry of 8,9-anhydroerythromycin a 6,9-hemiketal analogues with anti-mrsa and -vre activity Academic Article
- Design, synthesis, and biological evaluation of platensimycin analogues with varying degrees of molecular complexity Academic Article
- Discovery of novel antibacterial agents active against methicillin-resistant Staphylococcus aureus from combinatorial benzopyran libraries Academic Article
- Optimization and mechanistic studies of psammaplin a type antibacterial agents active against methicillin-resistant staphylococcus aureus (MRSA) Academic Article
- Redesign of glycopeptide antibiotics: back to the future Academic Article