| Literature DB >> 27267000 |
Mariagrazia Roselli1, Alessia Carocci2, Roberta Budriesi3, Matteo Micucci3, Maddalena Toma1, Lorenzo Di Cesare Mannelli4, Angelo Lovece1, Alessia Catalano1, Maria Maddalena Cavalluzzi1, Claudio Bruno1, Annalisa De Palma5, Marialessandra Contino1, Maria Grazia Perrone1, Nicola Antonio Colabufo1, Alberto Chiarini3, Carlo Franchini1, Carla Ghelardini4, Solomon Habtemariam6, Giovanni Lentini1.
Abstract
Four mexiletine analogues have been tested for their antiarrhythmic, inotropic, and chronotropic effects on isolated guinea pig heart tissues and to assess calcium antagonist activity, in comparison with the parent compound mexiletine. All analogues showed from moderate to high antiarrhythmic activity. In particular, three of them (1b,c,e) were more active and potent than the reference drug, while exhibiting only modest or no negative inotropic and chronotropic effects and vasorelaxant activity, thus showing high selectivity of action. All compounds showed no cytotoxicity and 1b,c,d did not impair motor coordination. All in, these new analogues exhibit an interesting cardiovascular profile and deserve further investigation.Entities:
Keywords: Antiarrhythmics; Inotropism; MW-assisted synthesis; Mexiletine; P-glycoprotein
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Year: 2016 PMID: 27267000 DOI: 10.1016/j.ejmech.2016.05.046
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514