Abstract |
Nine new N-acyl derivatives of 2-amino-1-alcohols and 1-amino-2-alcohols with a potential arrhythmic activity have been obtained. In the preliminary screening 2-[N-(7-theophyllineacetyl)-amino]-2-methyl-1- propanol, 5, was more active in the chloroform-induced arrhythmia than quinidine. Unlike to propranolol and quinidine, compound 5 in doses of 5-30 mg/kg, iv, did not prevent distortions of the cardiac rhythm evoked by adrenaline and strophanthine. When administered at the peak of arrhythmia, it did not abolish disturbances of the cardiac rhythm. Compound 5 had a low toxicity (LD50 = 3000 mg/kg, ip), did not change the control ECG curve, showed no cardiodepressive activity, and had weaker local anesthetic properties than lignocaine.
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Authors | M Eckstein, M Cegła, J Krupińska, B Cebo, M Michna |
Journal | Polish journal of pharmacology and pharmacy
(Pol J Pharmacol Pharm)
1987 May-Jun
Vol. 39
Issue 3
Pg. 317-22
ISSN: 0301-0244 [Print] Poland |
PMID | 3438214
(Publication Type: Journal Article)
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Chemical References |
- Amino Alcohols
- Anti-Arrhythmia Agents
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Topics |
- Amino Alcohols
(pharmacology)
- Animals
- Anti-Arrhythmia Agents
- Drug Evaluation, Preclinical
- Guinea Pigs
- In Vitro Techniques
- Male
- Mice
- Rats
- Rats, Inbred Strains
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