Entry into a new class of protein kinase inhibitors by pseudo ring design
Pascal Furet1, Giorgio Caravatti, Vito Guagnano
1Novartis Institutes for BioMedical Research, WKL-136.P.12, CH-4002 Basel, Switzerland. pascal.furet@novartis.com
Bioorganic & Medicinal Chemistry Letters
|February 6, 2008
Abstract:
A pyrimidin-4-yl-urea motif forming a pseudo ring by intramolecular hydrogen bonding has been designed to mimic the pyrido[2,3-d]pyrimidin-7-one core structure of a well-established class of protein kinase inhibitors. Potent inhibition of a number of protein kinases was obtained with the first prototype compound synthesized to probe the design concept.
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