ELECTROMECHANICAL EFFECTS OF NEWLY SYNTHESIZED PROPAFENONE DERIVATIVES ON ISOLATED GUINEA-PIG HEART-MUSCLE PREPARATIONS

Citation
C. Studenik et al., ELECTROMECHANICAL EFFECTS OF NEWLY SYNTHESIZED PROPAFENONE DERIVATIVES ON ISOLATED GUINEA-PIG HEART-MUSCLE PREPARATIONS, Arzneimittel-Forschung, 46(2), 1996, pp. 134-138
Citations number
15
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
ISSN journal
00044172
Volume
46
Issue
2
Year of publication
1996
Pages
134 - 138
Database
ISI
SICI code
0004-4172(1996)46:2<134:EEONSP>2.0.ZU;2-9
Abstract
Inotropic, chronotropic and beta-adrenoceptor blocking activities of t he newly synthetized propafenone derivatives amino-2-hydroxypropoxy)ph enyl-3-phenyl-1-propanone hydrochloride (AM 03), -(1-piperidyl)propoxy )phenyl)-3-phenyl-1-propanone hydrochloride (AM 05), thyl-N-(2-hydroxy -3-(2-(3-phenylpropionyl)phenoxy) propyl)-propylammonium iodide (TH 41 ), N,N-diethyl-N-(2 -(3-phenylpropionyl)phenoxy)propyl)-methylammonium iodide (AM 07), and -(3-phenylpropionyl)phenoxy)propyl)-methylammoniu m iodide (AM 09) studied in isolated, electrically stimulated papillar y muscles and spontaneously beating right atria of guinea pigs. In com parison with propafenone the tertiary amines AM 03 and AM 05 showed a higher negative inotropic potency, while the quarternary amines TH 41, AM 07 and AM 09 were less effective. With regard to their negative ch ronotropic action, AM 03 and AM 05 were more and TH 41, AM 07 and AM 0 9 less potent than the parent drug. In contrast to propafenone none of its derivatives exerted beta-adrenoceptor blockade at the concentrati ons studied.