Cytotoxic and anti-HIV phenanthroindolizidine alkaloids from Cryptocarya chinensis

Tian Shung Wu, Chung Ren Su, Kuo Hsiung Lee

研究成果: Article同行評審

17 引文 斯高帕斯(Scopus)

摘要

Bioassay-guided fractionation of the cytotoxic ethanol extract of Cryptocarya chinensis has led to the isolation of 11 compounds, including two phenanthroindolizidine alkaloids [(-)-antofine (1) and dehydroantofine (2)], five pavine alkaloids (3-7), and four proaporphine alkaloids (8-11). The structures of the isolated compounds were determined by means of NMR spectroscopic methods, and supported by HRMS and optical rotation data. Compounds 1 and 2 showed cytotoxic activity against four cancer cell lines, L1210, P388, A549, and HCT-8, with 1 being the most potent against A549 and HCT-8 with EC50 values of 0.002 and 0.001 μg/mL, respectively. In addition, 2 is first reported to exhibit significant anti-HIV activity.

原文English
頁(從 - 到)725-727
頁數3
期刊Natural Product Communications
7
發行號6
DOIs
出版狀態Published - 2012 六月

All Science Journal Classification (ASJC) codes

  • 藥理
  • 藥物發現
  • 植物科學
  • 補充和替代醫學

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