From the insoluble dye indirubin towards highly active, soluble CDK2-inhibitors

被引:78
作者
Jautelat, R [1 ]
Brumby, T
Schäfer, M
Briem, H
Eisenbrand, G
Schwahn, S
Krüger, M
Lücking, U
Prien, O
Siemeister, G
机构
[1] Schering AG, Med Chem, Res Ctr Europe, D-13342 Berlin, Germany
[2] Schering AG, ET Struct Biol, Res Ctr Europe, D-13342 Berlin, Germany
[3] Schering AG, CDCC Computat Chem, Res Ctr Europe, D-13342 Berlin, Germany
[4] Univ Kaiserslautern, Dept Chem, Div Food Chem & Environm Toxicol, D-67663 Kaiserslautern, Germany
[5] Schering AG, Corp Res, Expt Oncol, D-13342 Berlin, Germany
关键词
biological activity; enzymes; medicinal chemistry; natural products; structure-activity relationships;
D O I
10.1002/cbic.200400108
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In search of novel antitumor therapies. The natural product indirubin (1) is one of the class of indigo dyes, insoluble in aqueous systems, employed by mankind since the Bronze Age for textile coloring. In 1999 indirubin was reported to be a modest inhibitor of the enzyme CDK2, a key target in the ongoing search for novel antitumor therapies. With the guidance of X-ray structures, indirubin was transformed to yield novel, soluble, almost colorless, highly potent CDK2 inhibitors that strongly inhibit the growth of the MCF7 tumor cell line in vitro. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:531 / 540
页数:10
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