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      Anti-fungal effects of phenolic amides isolated from the root bark of Lycium chinense.

      Biotechnology Letters
      Amides, pharmacology, Antifungal Agents, Biotechnology, Caffeic Acids, chemistry, Candida albicans, metabolism, Coumaric Acids, Erythrocytes, drug effects, Hemolysis, Humans, Lycium, Magnetic Resonance Spectroscopy, Models, Chemical, Octopamine, analogs & derivatives, Plant Bark, Plant Extracts, Saccharomyces cerevisiae, Trichosporon, Tyramine

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          Abstract

          Four phenolic amides, dihydro-N-caffeoyltyramine (1), trans-N-feruloyloctopamine (2), trans-N -caffeoyltyramine (3), and cis-N-caffeoyltyramine (4), were isolated from an ethyl acetate extract of the root bark of Lycium chinense Miller. All had an anti-fungal effect; compounds 1-3 were potent at 5-10 microg ml(-1) and were without hemolytic activity against human erythrocyte cells. Compound 4 was active at 40 microg ml(-1). All four compounds impeded the dimorphic transition of pathogen, Candida albicans.

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