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Synthesis and biological activity of 2-anilino-4-(1H-pyrrol-3-yl) pyrimidine CDK inhibitors
Authors:Wang Shudong  Wood Gavin  Meades Christopher  Griffiths Gary  Midgley Carol  McNae Iain  McInnes Campbell  Anderson Sian  Jackson Wayne  Mezna Mokdad  Yuill Rhoda  Walkinshaw Malcolm  Fischer Peter M
Institution:Cyclacel Limited, James Lindsay Place, Dundee DD1 5JJ, Scotland, UK. swang@cyclacel.com
Abstract:A series of 2-anilino-4-(1H-pyrrol-3-yl)pyrimidines were prepared and evaluated for their ability to inhibit cyclin-dependent kinases (CDKs). A number of analogues were found to be potent CDK2 and CDK4 inhibitors and to exhibit anti-proliferative activity against human tumour cell lines. Structure-activity relationships and biochemical characterization are presented.
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