Synthesis and Antiarrhythmic and Hemostatic Activity of [3,3-Dialkyl-3, 4-Dihydroisoquinolin-1(2H )-Ylidene]-N-Alkylacetamides
- Authors: Gashkova O.V.1, Mikhailovskii A.G.1, Rudakova I.P.1, Starkova A.V.1, Yusov A.S.1
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Affiliations:
- Perm State Pharmaceutical Academy
- Issue: Vol 53, No 6 (2019)
- Pages: 507-510
- Section: Article
- URL: https://journals.rcsi.science/0091-150X/article/view/245833
- DOI: https://doi.org/10.1007/s11094-019-02028-6
- ID: 245833
Cite item
Abstract
[3,3-Dialkyl-3,4-dihydroisoqinolin-1(2H)-ylidene]-N-alkylacetamides were synthesized by reacting dialkylbenzylcarbinols with N-alkylcyanoacetamides. Hydrochlorides of the synthesized compounds existed in the imine form. All hydrochlorides showed antiarrhythmic and coagulant (hemostatic) effects. An amide with an unsubstituted amide N atom and a 3-spiro-cyclopentyl moiety was the most active compound with antiarrhythmic activity 2.8 times that of lidocaine and blood coagulation accelerated by 37.9%, which was 21.9% faster than etamsylate.
About the authors
O. V. Gashkova
Perm State Pharmaceutical Academy
Email: ajm@perm.ru
Russian Federation, Perm, 614990
A. G. Mikhailovskii
Perm State Pharmaceutical Academy
Author for correspondence.
Email: ajm@perm.ru
Russian Federation, Perm, 614990
I. P. Rudakova
Perm State Pharmaceutical Academy
Email: ajm@perm.ru
Russian Federation, Perm, 614990
A. V. Starkova
Perm State Pharmaceutical Academy
Email: ajm@perm.ru
Russian Federation, Perm, 614990
A. S. Yusov
Perm State Pharmaceutical Academy
Email: ajm@perm.ru
Russian Federation, Perm, 614990