Development of Pantothenate Analogs That Can Treat Combat-Related Infections
Abstract
We solved the co-crystal structures of SaPanK with MT-190 and KpPanK with MT-183. Based on these structures, we synthesized 11 new compounds that fit to the Pan analog binding site of SaPanK or KpPanK. In addition, we showed qualitative bacterial killing efficiency of these 11 compounds by agar diffusion and their cytotoxicity to HepG2 cells. These new compounds will be the basis for further optimization to develop a novel class of narrow-spectrum antibiotics against the multidrug resistant strains of S. aureus and K. pneumoniae.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jan 01, 2013
- Accession Number
- ADA581554
Entities
People
- Hee-won Park
Organizations
- University of Toronto