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Preventive and therapeutic agent for disorders caused by toxicity of quinone body or quinone precursor

机译:醌体或醌前体毒性引起的疾病的预防和治疗剂

摘要

PROBLEM TO BE SOLVED: To provide a medical agent effective to toxicity originated from a quinone compound or a precursor of quinone compound produced by oxidation of an exotic medical agent, or endogenous amines, amino acids or proteins, and specifically effective to cranial neuropathy and/or cytopathy.;SOLUTION: The invention relates to the suppressant of toxicity due to the quinone compound or precursor of the quinone compound comprising a compound selected from a group comprising dopamine receptor agonist (dopamine agonist). Dopamine receptor agonist such as bromocriptine mesilate, pergolide mesilate, talipexole hydrochloride, ropinirole hydrochloride, pramipexole hydrochloride, etc., has activities directly bonding to dopamine quinone compound or dopa quinone compound itself, and capturing and erasing. The suppressant exerts an excellent suppressing effect in a group administered with levodopa on cranial neuropathy caused by production of intracerebral quinone compounds.;COPYRIGHT: (C)2006,JPO&NCIPI
机译:解决的问题:提供一种对由醌化合物或醌化合物的前体产生的毒性有效的药物,该醌化合物或醌化合物的前体是由外来药物或内源性胺,氨基酸或蛋白质的氧化产生的,并且对颅神经病和/解决方案:本发明涉及毒性抑制剂,该毒性抑制剂归因于醌化合物或醌化合物的前体,所述醌化合物或醌化合物的前体包含选自多巴胺受体激动剂(多巴胺激动剂)的化合物。多巴胺受体激动剂如溴隐亭甲磺酸酯,甲磺酸培高利特,盐酸他利普索,盐酸罗匹尼罗,盐酸普拉克索等具有直接键合到多巴胺醌化合物或多巴醌化合物本身的活性,并被捕获和擦除。该抑制剂在左旋多巴给药组中对由脑内醌类化合物产生而引起的颅神经病变具有优异的抑制作用。;版权所有:(C)2006,JPO&NCIPI

著录项

  • 公开/公告号JP4734560B2

    专利类型

  • 公开/公告日2011-07-27

    原文格式PDF

  • 申请/专利权人 国立大学法人 岡山大学;

    申请/专利号JP20050027094

  • 发明设计人 浅沼 幹人;小川 紀雄;宮崎 育子;

    申请日2005-02-02

  • 分类号A61K31/4045;A61K31/428;A61K31/4745;A61K31/48;A61P39/02;

  • 国家 JP

  • 入库时间 2022-08-21 18:20:06

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