Maj J, Sowińska H, Baran L, Mogilnicka E, Przewłocka B
Pol J Pharmacol Pharm. 1980 Nov-Dec;32(6):823-32.
Craviten (M-71) or 2S, 2'S) N, N'-dimethyl-N, N'-bis [1-(3', 4', 5' -trimethoxy-benzoyloxy)-butyl-2]-ethylenediamine dihydrochloride an agent with a strong antiarrhythmic action has practically no effect on the central nervous system of rats and mice. It exerts no effect on the spontaneous motor activity, on amphetamine-stimulated hyperactivity, on rota-red performance, it has no analgesic and anticonvulsant action and does not change the hexobarbital sleeping time. No effects of Craviten were observed on the body temperature in rats and mice. It decreased the arterial blood pressure in rats and stimulated slightly respiration. The hypotensive effect was dose-dependent. The LD50 of the preparation is: rats: 142 mg/kg ip, 15 x 8 mg/kg iv; mice: 550 mg/kg ip; rabbits: 5 x 1 mg/kg iv.
克拉维亭(M - 71),即(2S,2'S)-N,N'-二甲基-N,N'-双[1 -(3',4',5'-三甲氧基苯甲酰氧基)-丁基-2]-乙二胺二盐酸盐,一种具有强大抗心律失常作用的药物,对大鼠和小鼠的中枢神经系统实际上没有影响。它对自发运动活动、对苯丙胺刺激的多动、对旋转棒性能均无影响,没有镇痛和抗惊厥作用,也不会改变戊巴比妥睡眠时间。未观察到克拉维亭对大鼠和小鼠体温有影响。它可降低大鼠的动脉血压并轻微刺激呼吸。降压作用呈剂量依赖性。该制剂的半数致死量为:大鼠:腹腔注射142毫克/千克,静脉注射15×8毫克/千克;小鼠:腹腔注射550毫克/千克;兔子:静脉注射5×1毫克/千克。