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Selective inhibition of complement membrane attack complex and C3 convertase by low molecular weight components of aurintricarboxylic acid synthesis complex

机译:金三羧酸合成配合物的低分子量成分对补体膜攻击复合物和C3转化酶的选择性抑制

摘要

A component of the aurintricarboxylic acid complex with a molecular weight of less than 1 kilodalton is used to selectively inhibit complement membrane attack complexes in mammalian species, preferably humans. Preferred inhibitors are aurin tricarboxylic acid, aurine adracarboxylic acid, and aurin hexacarboxylic acid. Preferred diseases to be treated by selective inhibition of complement membrane attack complexes are age-related macular degeneration, Alzheimer's disease, atherosclerosis, rheumatoid arthritis, paroxysmal nocturnal hemoglobinuria, malaria infection, and Multiple sclerosis.
机译:分子量小于1千道尔顿的金三羧酸复合物的组分用于选择性抑制哺乳动物物种,优选人类中的补体膜攻击复合物。优选的抑制剂是金黄色三羧酸,金黄色金羧酸和金红色六羧酸。通过选择性抑制补体膜攻击复合物治疗的优选疾病是年龄相关性黄斑变性,阿尔茨海默氏病,动脉粥样硬化,类风湿关节炎,阵发性夜间血红蛋白尿,疟疾感染和多发性硬化症。

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