Author/Authors :
Ravindra N. Guthikonda، نويسنده , , Shrenik K. Shah، نويسنده , , Stephen G. Pacholok، نويسنده , , John L. Humes، نويسنده , , Richard A. Mumford، نويسنده , , Stephan K. Grant، نويسنده , , Renee M. Chabin، نويسنده , , Barbara G. Green، نويسنده , , Nancy Tsou، نويسنده , , Richard Ball، نويسنده , , Daniel S. Fletcher، نويسنده , , Silvi Luell، نويسنده , , D. Euan MacIntyre، نويسنده , , Malcolm MacCoss، نويسنده ,
Abstract :
Syntheses and nitric oxide synthase inhibitory activity of cyclic amidines containing 5,6- 6,6- and 7,6-fused systems are described. X-ray structure determination facilitated the assignment of the stereochemistry of the most active compounds perhydro-2-iminoisoquinoline (8a) and perhydro-2-iminopyrindine (10a). Both 8a and 10a are very potent inhibitors of iNOS, with excellent selectivity over eNOS and they are orally active in rats with long duration suitable for once or twice a day dosing.