Synthesis and antitumor activity of 3- and 5-hydroxy-4-methylpyridine-2-carboxaldehyde thiosemicarbazones
作者:Yuqiang Wang、Mao Chin Liu、Tai Shun Lin、Alan C. Sartorelli
DOI:10.1021/jm00098a011
日期:1992.10
hyde thiosemicarbazone (5-HMP), of 5-hydroxypyridine-2-carboxaldehyde thiosemicarbazone (5-HP) have been designed and synthesized by two different methods. 3-HMP and 5-HMP both showed better antitumor activity than their respective parent compounds, 3-hydroxypyridine-2-carboxaldehyde thiosemicarbazone and 5-HP, in mice bearing the L1210 leukemia.
为了开发具有临床实用性的α-(N)-杂环羧醛硫代半碳酰胺,两个类似物3-羟基-4-甲基吡啶-2-羧醛硫代半碳酮(3-HMP)和5-羟基-4-甲基吡啶-2通过两种不同的方法设计和合成了5-羟基吡啶-2-羧甲醛硫代半碳酮(5-HP)的-甲醛甲醛硫代半碳酮(5-HMP)。在携带L1210白血病的小鼠中,3-HMP和5-HMP均显示出比其各自的母体化合物3-羟基吡啶-2-羧甲醛硫半乳糖和5-HP更好的抗肿瘤活性。