Four New Lignans from Kadsura Interior and Their Bioactivity
- Molecules. 2018 May 26;23(6):1279. doi: 10.3390/molecules23061279.
- 1. Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China. [email protected].
- 2. Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China. [email protected].
- 3. Institute of Traditional Chinese Medicine, Xinjiang Medical University, Urumqi 830011, China. [email protected].
- 4. Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China. [email protected].
- 5. Institute of Traditional Chinese Medicine, Xinjiang Medical University, Urumqi 830011, China. [email protected].
- 6. Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China. [email protected].
- 7. Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China. [email protected].
A phytochemical investigation of the stems of Kadsura interior has led to an isolation of four new Lignans, named kadsutherin E⁻H (1⁻4), together with two known Lignans (5⁻6). The structures of the four new compounds were established on the basis of comprehensive spectroscopic analyses. Compounds 1⁻6 exhibited inhibition against adenosine diphosphate (ADP) induced platelet aggregation. Among the isolated compounds, kadsutherin F (2) showed the strongest anti-platelet aggregation activity with an inhibition of 49.47%.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: OthersResearch Areas: Cardiovascular Disease
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target: OthersResearch Areas: Cardiovascular Disease