化学
胺气处理
还原胺化
细胞培养
选择性
化学合成
胺化
立体化学
叔胺
结构-活动关系
体外
IC50型
生物活性
组合化学
生物化学
有机化学
催化作用
生物
遗传学
作者
Dominika Czerwonka,Ewa Maj,Joanna Wietrzyk,Adam Huczyński
标识
DOI:10.1016/j.bmcl.2021.128382
摘要
A series of 22 amine analogs of thiocolchicine were synthesized using the reductive amination reaction. The antiproliferative activities of these compounds were tested against four tumor cell lines as well as one normal cell line. The tested analogs exhibited IC50 values in the nanomolar range accompanied by high selectivity indexes, and most importantly, they were able to break the drug resistance of the human colon adenocarcinoma resistant cell line (LoVo/DX). Also, a correlation between the antiproliferative activity and physicochemical properties of the novel compounds has been found.
科研通智能强力驱动
Strongly Powered by AbleSci AI