摘要

The Mannich-based analogues of S-(+)-curcuphenol (1), 3a-5a, and 3b potently inhibited the growth of several NCI's human cancer cell lines. In addition, 7a showed a 12-fold antimigratory activity (IC50 3.1 mu M) against the human breast cancer cell line MDA-MB-231 compared to its parent 1 (IC50 37.2 mu M).

  • 出版日期2012-10