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Solinski AE , Koval AB , Brzozowski RS , Morrison KR , Fraboni AJ , Carson CE , Eshraghi AR , Zhou G , Quivey RG Jr , Voelz VA , Buttaro BA , Wuest WM
Diverted Total Synthesis of Carolacton-Inspired Analogs Yields Three Distinct Phenotypes in Streptococcus mutans Biofilms
J Am Chem Soc. 2017 May 31;139(21) :7188-7191
PMID: 28502178 PMCID: PMC5891724 URL: https://www.ncbi.nlm.nih.gov/pubmed/28502178
AbstractThe oral microbiome is a dynamic environment inhabited by both commensals and pathogens. Among these is Streptococcus mutans, the causative agent of dental caries, the most prevalent childhood disease. Carolacton has remarkably specific activity against S. mutans, causing acid-mediated cell death during biofilm formation; however, its complex structure limits its utility. Herein, we report the diverted total synthesis and biological evaluation of a rationally designed library of simplified analogs that unveiled three unique biofilm phenotypes further validating the role of natural product synthesis in the discovery of new biological phenomena.
Notes1520-5126 Solinski, Amy E Koval, Alexander B Brzozowski, Richard S Morrison, Kelly R Fraboni, Americo J Carson, Carrie E Eshraghi, Anisa R Zhou, Guangfeng Quivey, Robert G Jr Voelz, Vincent A Buttaro, Bettina A Wuest, William M ORCID: http://orcid.org/0000-0002-5198-7744 Journal Article United States J Am Chem Soc. 2017 May 31;139(21):7188-7191. doi: 10.1021/jacs.7b03879. Epub 2017 May 17.