Journal
JOURNAL OF NATURAL PRODUCTS
Volume 78, Issue 4, Pages 597-603Publisher
AMER CHEMICAL SOC
DOI: 10.1021/np5003252
Keywords
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Funding
- TGIR-RMN-THC FR CNRS [3050]
- Egide
- CNRS
- Conseil Regional Champagne Ardenne
- Conseil General de la Marne
- Ministry of Higher Education and Research (MESR)
- EU-Programme FEDER
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Two heterodimers comprising anthraquinone and methylbenzoisocoumarin moieties (1 and 2) were isolated, together with emodin and physcion from the tubers of Pyrenacantha kaurabassana. The structures of 1 and 2 were established by NMR spectroscopy, including the analysis of a 2D INADEQUATE spectrum. On the basis of the data obtained, the structures that were previously proposed in the literature for these compounds were revised. Compounds 1 and 2 showed antibacterial activity against three different strains of Staphylococcus aureus. Compound 2 also showed bactericidal activity against Helicobacter pylori.
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