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Craviten hydrolysis in vitro was studied in human, rat and canine plasma and erythrocytes. Craviten was degraded during the… Expand Craviten was given iv in four different doses into male Wistar rats and tissue concentration of that drug was determined… Expand A method has been evolved for determination of Craviten and its degradation products making possible qualitative investigations… Expand The studies of chronic toxicity of the preparation M-71 (Craviten) were carried out on rats and mice. The body weight, absolute… Expand Craviten (M-71) or 2S, 2'S) N, N'-dimethyl-N, N'-bis [1-(3', 4', 5' -trimethoxy-benzoyloxy)-butyl-2]-ethylenediamine… Expand Preparation M-71 (Craviten, Polfa) possesses strong antiarrhythmic properties. It prevents development of cardiac arrhythmia… Expand Craviten (M-71) increases the coronary flow, depresses the rate of contractions, and transiently depresses the contractile force… Expand A spectrofluorometric method for the quantitative determination of Craviten in serum, tissues and urine is described. The… Expand Serum and urine levels of iv administered Craviten were determined. Comparison of the decline of the same absolute and relative… Expand Craviten, a newly synthesized ester of optically active 2-aminobutanol-1, produced in cats hypotension and inhibited excitability… Expand