Quinazolines: Combined type 3 and 4 phosphodiesterase inhibitors

B Charpiot, J Brun, I Donze, R Naef, M Stefani…

文献索引：Charpiot, Brigitte; Brun, Jvan; Donze, Irene; Naef, Reto; Stefani, Monique; Mueller, Thomas Bioorganic and Medicinal Chemistry Letters, 1998 , vol. 8, # 20 p. 2891 - 2896

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被引用次数: 56

摘要

A series of quinazolines has been prepared and evaluated for its ability to inhibit cyclic AMP phosphodiesterase type 3, type 4A, 4B and 4D. The most potent inhibitors showed IC50 values in the nanomolar range for type 3 and type 4 isoforms and bind with high affinity to the [3H] rolipram binding site. These quinazolines represent a new family of potent mixed PDE 3/4 inhibitors and are expected to have a therapeutic potential.