The anti-MRSA compound 3-O-alpha-L-(2″,3″-di-p-coumaroyl)rhamnoside (KCR) inhibits protein synthesis in Staphylococcus aureus-Reference-Cited by-同舟云学术

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The anti-MRSA compound 3-O-alpha-L-(2″,3″-di-p-coumaroyl)rhamnoside (KCR) inhibits protein synthesis in Staphylococcus aureus

Published:2020-01 Issue: Volume:210 Page:103539
ISSN:1874-3919
Container-title:Journal of Proteomics
language:en
Short-container-title:Journal of Proteomics

Author:

Carruthers Nicholas J.,Stemmer Paul M.,Media Joe,Swartz Ken,Wang Xiaojuan,Aube Nicholas,Hamann Mark T.,Valeriote Frederick,Shaw Jiajiu

Funder

National Institutes for Health

Abney Foundation

Publisher

Elsevier BV

Subject

Biochemistry,Biophysics

Reference51 articles.

1. Antimicrobial resistance trends and outbreak frequency in United States hospitals;Diekema;Clin. Infect. Dis.,2004

2. What is MRSA?;Pantosti;Eur. Respir. J.,2009

3. Staphylococcus aureus in dermatology outpatients with special emphasis on community-associated methicillin-resistant strains;Jappe;J. Invest. Dermatol.,2008

4. The management of infection and colonization due to methicillin-resistant Staphylococcus aureus: a CIDS/CAMM position paper;Simor;Can. J. Infect. Dis.,2004

5. Impact of infection control interventions and antibiotic use on hospital MRSA: a multivariate interrupted time-series analysis;Mahamat;Int. J. Antimicrob. Agents,2007

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