Synthesis and biological testing of purine derivatives as potential ATP-competitive kinase inhibitors

被引:102
作者
Laufer, SA
Domeyer, DM
Scior, TRF
Albrecht, W
Hauser, DRJ
机构
[1] Univ Tubingen, Dept Pharmaceut & Med Chem, D-72076 Tubingen, Germany
[2] Merckle GmbH, D-89079 Ulm, Germany
[3] Benemerita Univ Autonoma Puebla, Dept Pharm, Puebla 72570, Mexico
关键词
D O I
10.1021/jm0408767
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
On the basis of ATP adenine, a series of adenine and purine derivatives was prepared and tested for their ability to inhibit a spectrum of disease-related kinases. There has been scant research investigating the potential of cosubstrate derived kinase inhibitors for other kinases than CDKs. Our inhibitor design combined the purine system from the original cosubstrate ATP and phenyl moieties in order to explore possible interactions with the different regions of the ATP binding site in several disease-related protein kinases. There have been a number of hits for the assayed substances, which led us to conclude that the spectrum of compounds may prove to be a valuable tool kit for the evaluation of bonding and selectivity patterns for a wide variety of kinases.
引用
收藏
页码:710 / 722
页数:13
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