Found 1 publication.
Displayed publication 1
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 8155)
Herath HM, Jacob M, Wilson AD, Abbas HK, Nanayakkara NP
New secondary metabolites from bioactive extracts of the fungus Armillaria tabescens
Natural Product Research 27(17) (2013)
1562-1568
Ethyl acetate extracts of Armillaria tabescens (strain JNB-OZ344) showed significant fungistatic and bacteristatic activities against several major human pathogens including Candida albicans, Cryptococcus neoformans, Escherichia coli and Mycobacterium intracellulare. Chemical analysis of these extracts led to the isolation and identification of four new compounds, emestrin-F (1), emestrin-G (2), 6-O-(4-O-methyl-β-D-glucopyranosyl)-8-hydroxy-2,7-dimethyl-4H-benzopyran-4-one (3) and cephalosporolide-J (4), along with five other previously known compounds, emestrin (5), cephalosporolide-E (6), decarestrictine-C2 (7), ergosterol and brassicasterol. Structural elucidation of all compounds was carried out by NMR and MS analyses. Antimicrobial assays revealed that compounds 1 and 5 were responsible for the observed growth inhibitory activities of the fungal extracts against the human pathogens tested.
antimicrobial activity, Armillaria tabescens, emestrin, chromone, cephalosporolide
NCBI PubMed ID: 23140424Publication DOI: 10.1080/14786419.2012.738206Journal NLM ID: 101167924Publisher: Milton Park, UK : Taylor & Francis Health Sciences
Correspondence: Nanayakkara NP
olemiss.edu>
Institutions: National Center for Natural Products Research, School of Pharmacy, University of Mississippi, MS, USA, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, MS, USA, Center for Bottomland Hardwoods Research, USDA-Forest Service, Southern Hardwood Laboratory, Stoneville, MS, USA, Crop Genetics and Production Research Unit, USDA-ARS, Stoneville, MS, USA
Methods: 13C NMR, 1H NMR, TLC, HR-ESI-MS, HMBC, HMQC, COSY
The publication contains the following compound(s):
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: <1 sec