双氯洛酚和阿利莫洛酚:治疗蛋白质错误折叠障碍、神经病变和神经性疼痛的热休克蛋白共同诱导剂

K. Jm
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引用次数: 6

摘要

bimoclool和arimoclool是上世纪末由匈牙利Biorex制药公司合成的小型新型化学实体。在一系列动物模型中,这两种化合物一致增加热休克蛋白(HSP)的表达,降低功能和结构病理。双氯酚的发展停滞不前,很可能是由于化合物的半衰期短。阿利莫洛莫目前正在开发用于孤儿疾病,如肌萎缩性侧索硬化症、鞘脂性Niemann- Pick型C和包涵体肌炎。阿利莫洛尔口服有效度高,中枢神经系统穿透力好,不会引起中枢神经系统的副作用。由于其神经保护和镇痛特性,它也可能是治疗糖尿病神经病变和(糖尿病)神经病变神经性疼痛的有前途的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bimoclomol and Arimoclomol: HSP-co-Inducers for the Treatment of ProteinMisfolding Disorders, Neuropathy and Neuropathic Pain
Bimoclomol and arimoclomol are small new chemical entities which have been synthesized during the end of last century by a Hungarian pharmaceutical company, Biorex. Both compounds consistently increase Heat Shock Protein (HSP) expression and reduce functional as well as structural pathology in a series of animal models. The development of bimoclomol stagnated, most probably due the short half life time of the compound. Arimoclomol is currently in development for orphan disorders such as amyotrophic lateral sclerosis, the sphingolipidose Niemann- Pick type C and inclusion body myositis. Arimoclomol has high oral availability and good CNS penetration, without inducing troublesome CNS side effects. It might also be a promising compound for the treatment of diabetic neuropathy and neuropathic pain in (diabetic) neuropathy, due to its neuroprotective and analgesic properties.
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