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Antibacterial compounds from Salvia adenophora Fernald (Lamiaceae)
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2831948
Author(s) Bisio, A.; Schito, A. M.; Ebrahimi, S. N.; Hamburger, M.; Mele, G.; Piatti, G.; Romussi, G.; Dal Piaz, F.; De Tommasi, N.
Author(s) at UniBasel Hamburger, Matthias
Ebrahimi, Samad
Year 2015
Title Antibacterial compounds from Salvia adenophora Fernald (Lamiaceae)
Journal Phytochemistry
Volume 110
Pages / Article-Number 120-32
Keywords Lamiaceae, Salvia adenophora Fernald, ECD, Clerodane diterpenes, Derivatives of 12-oxo-phytodienoic acid, Antimicrobial activity
Abstract From the aerial parts of Salvia adenophora Fernald four derivatives of 12-oxo-phytodienoic acid (1-4) together with five clerodane diterpenoids (5,6,8-10), and one known diterpene (7) have been isolated. Compounds 1-6 and 8-10 are described for the first time. The structures were established by extensive 1D, 2D NMR and HRESI-TOFMS spectroscopic methods. Finally, the absolute configuration has been established by comparing of experimental and quantum chemical calculation of ECD spectra. Despite a total lack of antimicrobial activity of the plant extract, hinting to the existence of antagonistic interactions in the crude material, three oxylipins (2-4) displayed a promising inhibition on Gram-positive multidrug-resistant clinical strains including Staphylococcus aureus, Streptococcus agalactiae and, particularly, Staphylococcus epidermidis, while the compounds 9 and 10 revealed a specific and strain-dependent activity against S. epidermidis. Interestingly, the inhibition provided by these compounds was independent of the resistance patterns of these pathogens to classic antibiotics. No action was reported on Gram-negative strains nor on Candida albicans. These results confirm that clerodanes and, particularly, prostaglandin-like compounds can be considered as interesting antimicrobial agents deserving further study. (C) 2014 Elsevier Ltd. All rights reserved.
Publisher Elsevier
ISSN/ISBN 0031-9422 ; 1873-3700
edoc-URL http://edoc.unibas.ch/dok/A6381773
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.phytochem.2014.10.033
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/25435172
ISI-Number WOS:000350921300013
Document type (ISI) Journal Article
 
   

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