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STRUCTURE-ACTIVITY RELATIONSHIP STUDY OF DITERPENES FOR TREATMENT OF ALZHEIMER'S DISEASE

机译:二异戊二烯治疗结构性与活动性的关系

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摘要

Alzheimer's disease is an irreversible, degenerative and age-related disease which is growing more and more with the increase in life expectancy. Kaurane diterpenes are a class of natural products available in large amounts in nature and isolated from plants grown worldwide. In the present work? twenty-seven kaurane diterpenes of natural origin and some readily available derivatives were assayed for acetylcholinesterase inhibition and the structure-activity relationship was analyzed. The kaurenoic acid derivatives screened showed to be promising inhibitors of AChE, which could provide new leads for drugs to fight Alzheimer's disease symptoms. Among them, eleven compounds showed activities comparable or higher than the positive control galantamine. Existence of an allylic hydroxyl group showed to be an important structural feature for AChE inhibition. In addition, presence of free hydroxyl groups at C-17 and C-19, furnished a diol especially active, able to completely inhibit AChE.
机译:阿尔茨海默氏病是一种不可逆的,退化性的且与年龄有关的疾病,随着预期寿命的增加,这种疾病越来越多。贝壳杉烷二萜是一类天然产物,可从自然界中大量获取,并从世界各地种植的植物中分离出来。在目前的工作中?分析了二十七种天然来源的月桂烷二萜和一些现成的衍生物对乙酰胆碱酯酶的抑制作用,并分析了其构效关系。筛选出的牛磺酸衍生物是AChE抑制剂,有望为对抗阿尔茨海默氏病症状的药物提供新的线索。其中,十一种化合物显示出与阳性对照加兰他敏相当或更高的活性。烯丙基羟基的存在被证明是抑制AChE的重要结构特征。另外,在C-17和C-19处存在游离羟基,提供了特别活跃的二醇,能够完全抑制AChE。

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