首页> 外国专利> Antiatherosclerotic medicament containing chromocarb (preferably as salt) and cyaninosides (preferably as flavylium salts), effective by retarding oxidative lipid metabolism and/or scavenging free radicals

Antiatherosclerotic medicament containing chromocarb (preferably as salt) and cyaninosides (preferably as flavylium salts), effective by retarding oxidative lipid metabolism and/or scavenging free radicals

机译:含有铬脲(优选为盐)和花青苷(优选为黄酮盐)的抗动脉粥样硬化药物,可通过抑制氧化脂质代谢和/或清除自由基而有效

摘要

Antiatherosclerotic medicament contains at least one chromone compound (I), selected from chromocarb (Ia) (preferably in the form of a chromone-2-carboxylic acid carboxylate salt) and cyaninosides (Ib) (preferably in the form of flavylium salts), for retarding oxidative metabolism of lipids circulating in the blood and/or scavenging anionic free radicals. An independent claim is also included for the use of (I) for the production of a medicament as above. ACTIVITY : Antiarteriosclerotic. In tests in genetically atherosclerotic mice, oral administration of chromocarb diethylamine salt (I'a) at 1.8 mg (or 40 mg/kg) per day for 3 days reduced the peroxidized lipid level by 54% and the surface area of aortic atherosclerotic lesions from 27917 Microm2 to 12500 Microm2 (both relative to untreated controls). MECHANISM OF ACTION : Oxidative lipid metabolism retardant; anionic free radical scavenger; synergist.
机译:抗动脉粥样硬化药物包含至少一种选自发色威(Ia)(优选以发色-2-羧酸羧酸盐的形式)和花青苷(Ib)(优选以黄酮盐的形式)的色酮化合物(I)。阻碍血液中循环脂质的氧化代谢和/或清除阴离子自由基。还包括关于(I)用于生产上述药物的用途的独立权利要求。活动:抗动脉硬化。在遗传性动脉粥样硬化小鼠的测试中,每天口服1.8mg(或40 mg / kg)的铬碳二乙胺盐(I'a)3天可使过氧化脂质水平降低了54%,主动脉粥样硬化病变的表面积从27917 Microm2>至12500 Microm2>(均相对于未处理的对照)。作用机理:氧化脂质代谢抑制剂;阴离子自由基清除剂;增效剂。

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