Structure–activity studies for a novel series of tricyclic dihydropyridopyrazolones and dihydropyridoisoxazolones as K ATP channel openers

• Published in: Bioorganic & medicinal chemistry Vol. 12; no. 8; pp. 1895 - 1904
• Main Authors: Drizin, Irene, Altenbach, Robert J., Buckner, Steven A., Whiteaker, Kristi L., Scott, Victoria E., Darbyshire, John F., Jayanti, Venkata, Henry, Rodger F., Coghlan, Michael J., Gopalakrishnan, Murali, Carroll, William A.
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 2004
• ISSN: 0968-0896; 1464-3391
• DOI: 10.1016/j.bmc.2004.01.038

In search of a novel chemotype of K ATP channel openers a series of tricyclic dihydropyridopyrazolones and dihydropyridoisoxazolones was synthesized. It was found that cyclopentanone in the left hand portion of the molecule was 4-fold more potent than cyclohexanone. Introduction of gem-dimethyl groups as well as incorporation of oxygen in the cyclohexanone ring in the left hand portion of the molecule increased the potency 10-fold. In the right hand portion of the molecule, the NH-group of the pyrazolone can be effectively substituted by oxygen increasing the activity 5-fold. Incorporation of a methyl group adjacent to the dihydropyridine (DHP) nitrogen not only significantly boosted activity, but also provided an additional benefit of increased metabolic stability. In vitro tests on the tissue from pig bladder strips provided further confirmation of K ATP activity of these compounds. SAR for a new class of K ATP channel openers is described. The compounds exhibited great potency and were metabolically stable.