首页> 外国专利> PROCESS FOR PREPARING 9*100DIHYDROERGOCINE AND PHYSIOLOGICALLY ACCEPTABLE ACID ADDITIVES THEREOF AND APPLICATION AS MEDICINE

PROCESS FOR PREPARING 9*100DIHYDROERGOCINE AND PHYSIOLOGICALLY ACCEPTABLE ACID ADDITIVES THEREOF AND APPLICATION AS MEDICINE

机译:制备9 * 100二氢古丁酸及其生理可接受的酸添加剂的方法及其在医学中的应用

摘要

(I) and its acid addn. salts are prepd. by hydrogenation of ergosine in dimethylformamide with shaking, at normal press., in the dark using a 10% Pd/C catalyst and opt. converting (I) to its salts. (I) is used to treat arterial hypertension, peripheral angiopathy, cerebral circulatory troubles, cardiac arrythmia and migraine. It is administered parenterally or enterally in daily doses of 0.3-10 7g/70 kg Acute toxicity (methanesulphonate i.p. in mice LD50=72.2 mg/kg, i.p. in rats=N400mg/kg) and pharmacological tests (arterial press., effect on heart, antiadrenaline effect, antiserotonin effect) are described. The reaction is effected rapidly reducing by-prods. due to degradation and giving high yields of (I).
机译:(I)及其酸加成。准备盐。通常情况下,在黑暗中使用10%Pd / C催化剂在摇晃下,将麦角碱在二甲基甲酰胺中氢化,然后选择将(I)转化为其盐。 (I)用于治疗动脉高压,周围血管病变,脑循环障碍,心律不齐和偏头痛。每天以0.3-10 7g / 70 kg的剂量经肠胃外或肠胃外给药急性毒性(小鼠ip50 LD50 = 72.2 mg / kg,甲磺酸ip = N400mg / kg ip)和药理学试验(动脉压,对心脏的影响) ,抗肾上腺素作用,抗5-羟色胺作用)。该反应可快速还原副产物。由于降解并得到高产率的(I)。

著录项

  • 公开/公告号JPS52156900A

    专利类型

  • 公开/公告日1977-12-27

    原文格式PDF

  • 申请/专利权人 LEK TOVARNA FARMACEVTSKIH;

    申请/专利号JP19770022900

  • 发明设计人 RUDORUFU RUKUMAN;NEBOISA DEIORUJIEBITSUKU;

    申请日1977-03-04

  • 分类号A61K31/48;A61P9/06;A61P9/12;A61P25/02;A61P43/00;C07D519/02;

  • 国家 JP

  • 入库时间 2022-08-22 23:09:01

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