Synthesis of a new series of purine derivatives and their anti-cyclin-dependent kinase activities
作者:Michel Legraverend、Odile Ludwig、Sophie Leclerc、Laurent Meijer
DOI:10.1002/jhet.5570380145
日期:2001.1
The synthesis of new purine derivatives designed to inhibit cell cycle regulating cyclin-dependent kinases (CDKs), is reported. These compounds, related to olomoucine and roscovitine, are characterised by the presence of apyrrolidine methanol substituent at C-2 and a variety of ortho, meta and/or para substituents on the C-6 arylamino group.
据报道,旨在抑制细胞周期调节细胞周期蛋白依赖性激酶(CDKs)的新嘌呤衍生物的合成。这些与olomoucine和roscovitine有关的化合物的特征在于在C-2处存在吡咯烷甲醇取代基以及在C-6芳基氨基上存在多种邻位,间位和/或对位取代基。