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多靶点神经保护化合物漆黄素的化学修饰。

Chemical modification of the multitarget neuroprotective compound fisetin.

机构信息

The Salk Institute for Biological Studies, 10010 N. Torrey Pines Road, La Jolla, California 92037, United States.

出版信息

J Med Chem. 2012 Jan 12;55(1):378-89. doi: 10.1021/jm2012563. Epub 2011 Dec 20.

Abstract

Many factors are implicated in age-related central nervous system (CNS) disorders, making it unlikely that modulating only a single factor will provide effective treatment. Perhaps a better approach is to identify small molecules that have multiple biological activities relevant to the maintenance of brain function. Recently, we identified an orally active, neuroprotective, and cognition-enhancing molecule, the flavonoid fisetin, that is effective in several animal models of CNS disorders. Fisetin has direct antioxidant activity and can also increase the intracellular levels of glutathione (GSH), the major endogenous antioxidant. In addition, fisetin has both neurotrophic and anti-inflammatory activity. However, its relatively high EC(50) in cell based assays, low lipophilicity, high topological polar surface area (tPSA), and poor bioavailability suggest that there is room for medicinal chemical improvement. Here we describe a multitiered approach to screening that has allowed us to identify fisetin derivatives with significantly enhanced activity in an in vitro neuroprotection model while at the same time maintaining other key activities.

摘要

许多因素与年龄相关的中枢神经系统(CNS)疾病有关,因此,仅调节单一因素不太可能提供有效的治疗方法。也许更好的方法是确定具有与维持大脑功能相关的多种生物学活性的小分子。最近,我们发现了一种具有口服活性、神经保护和认知增强作用的黄酮类化合物非瑟酮,它在几种中枢神经系统疾病的动物模型中都有效。非瑟酮具有直接的抗氧化活性,还可以增加细胞内谷胱甘肽(GSH)的水平,GSH 是主要的内源性抗氧化剂。此外,非瑟酮具有神经营养和抗炎活性。然而,它在基于细胞的测定中的相对较高的 EC(50)、低脂溶性、高拓扑极性表面积(tPSA)和较差的生物利用度表明,在药物化学方面还有改进的空间。在这里,我们描述了一种多层次的筛选方法,该方法使我们能够鉴定出在体外神经保护模型中具有显著增强活性的非瑟酮衍生物,同时保持其他关键活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e56a/3291199/00b4dc2304af/nihms356414f1.jpg

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