作者:Sun-Hee Lee、Sun-Kyoung Park、Jeong-Mi Kim、Myung-Hwa Kim、Kwang-Hee Kim、Kwang-Woo Chun、Kyung-Hea Cho、Ji-Youn Youn、Sung Keon Namgoong
DOI:10.1002/ardp.200500148
日期:2005.12
New thiocolchicine derivatives (1–8) were designed as less toxic anticancer agents possessing the power ful anticancer activity of colchicine. The synthesis and biological evaluation of these compounds were described. As a preliminary result of biological in vitro investigation, compounds 1, 6, and 7 showed lower toxicities than that of colchicine in combination with potent anticancer activities.
新的硫代秋水仙碱衍生物 (1-8) 被设计为毒性较低的抗癌剂,具有秋水仙碱的强大抗癌活性。描述了这些化合物的合成和生物学评价。作为体外生物学研究的初步结果,化合物 1、6 和 7 显示出比秋水仙碱更低的毒性和有效的抗癌活性。