Cardioselective Anti-Ischemic ATP-Sensitive Potassium Channel Openers. 3. Structure-Activity Studies on Benzopyranyl Cyanoguanidines; Modification of the …

…, SZ Ahmed, PG Sleph, S Dzwonczyk…

Index: Atwal, Karnail S.; Grover, Gary J.; Ahmed, Syed Z.; Sleph, Paul G.; Dzwonczyk, Steven; et al. Journal of Medicinal Chemistry, 1995 , vol. 38, # 17 p. 3236 - 3245

Full Text: HTML

Citation Number: 27

Abstract

Structure-activity relationships for the cyanoguanidine portion of the lead cardiac selective ATP-sensitive potassium channel (KATP) opener (3) are described. The cyanoguanidine moity appears to be optimal since increasing or decreasing the distance between the aniline nitrogen and the pendant aromatic ring attenuates anti-ischemic potency/selectivity. Similarly, unfavorable results are obtained by replacement of the aniline nitrogen with ...

Related Articles:

On the illusive nature of o-formylazobenzenes: Exploiting the nucleophilicity of the azo group for cyclization to indazole derivatives

[Rosevear, Judi; Wilshire, John F. K. Australian Journal of Chemistry, 1985 , vol. 38, # 5 p. 723 - 733]

Thermal decomposition of alkyl N-(o-nitrophenyl) carbamates: A novel synthesis of benzofurazan

[Prokipcak,J.M. et al. Canadian Journal of Chemistry, 1969 , vol. 47, # 13 p. 2482 - 2484]

More Articles...