Diverted Total Synthesis of Carolacton-Inspired Analogs Yields Three Distinct Phenotypes in Streptococcus mutans Biofilms-Reference-Cited by-同舟云学术

Diverted Total Synthesis of Carolacton-Inspired Analogs Yields Three Distinct Phenotypes in Streptococcus mutans Biofilms

Published:2017-05-17 Issue:21 Volume:139 Page:7188-7191
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Solinski Amy E.¹,Koval Alexander B.¹,Brzozowski Richard S.¹,Morrison Kelly R.¹,Fraboni Americo J.¹,Carson Carrie E.¹,Eshraghi Anisa R.¹,Zhou Guangfeng¹,Quivey Robert G.²,Voelz Vincent A.¹,Buttaro Bettina A.³,Wuest William M.¹^ORCID

Affiliation:

1. Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122, United States

2. Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester New York 14642, United States

3. Department of Microbiology and Immunology, Lewis Katz School of Medicine, Temple University, Philadelphia, Pennsylvania 19140, United States

Funder

Division of Chemistry

National Institute of Dental and Craniofacial Research

Temple University

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.7b03879

Reference32 articles.

1. Natural Products as Sources of New Drugs over the Last 25 Years

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4. A mammalian protein targeted by G1-arresting rapamycin–receptor complex

5. The Rhizosphere Microbiome: A Playground for Natural Product Chemists

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