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 μg ml -1 and were without hemolytic activity against human erythrocyte cells. Compound 4 was active at 40 μg ml -1. All four compounds impeded the dimorphic transition of pathogen, Candida albicans.
Original language | English |
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Pages (from-to) | 1125-1130 |
Number of pages | 6 |
Journal | Biotechnology Letters |
Volume | 26 |
Issue number | 14 |
DOIs | |
State | Published - Jul 2004 |
Keywords
- anti-fungal activity
- dihydro-N-caffeoyltyramine
- Lycium chinense
- Solanaceae
- trans-N-caffeoyltyramine
- trans-N-feruloyloctopamine