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托洛酮衍生物的合成及其体外神经保护活性的评价。

Synthesis of tropolone derivatives and evaluation of their in vitro neuroprotective activity.

机构信息

Institute of Organic and Pharmaceutical Chemistry, National Hellenic Research Foundation, 48 Vas Constantinou Ave, 116 35 Athens, Greece.

出版信息

Eur J Med Chem. 2010 Mar;45(3):1107-12. doi: 10.1016/j.ejmech.2009.12.006. Epub 2009 Dec 31.

Abstract

beta-Thujaplicin (hinokitiol or 2-hydroxy-4-isopropyl-2,4,6-cycloheptatrien-1-one), a natural tropolone, shows numerous activities while its synthetic analogues were found to exhibit anticancer and anti-ischemic activity. However, the ability of tropolone derivatives to protect neuronal cells from oxidative stress-induced cell damage has not been studied so far. As an ongoing effort toward highly effective antioxidants with potential neuroprotective activity, we have synthesized 7-substituted derivatives of beta-thujaplicin and its methoxy analogue. The substituents were heterocycles (piperazine, morpholine) or heteroaromatics (triazoles, pyridine). Only the piperazine derivatives of beta-thujaplicin were able to protect HT22 hippocampal neurons from oxidative stress-induced cell death.

摘要

β-雪松醇(桧醇或 2-羟基-4-异丙基-2,4,6-环庚三烯-1-酮),一种天然的三酮,具有多种活性,而其合成类似物则具有抗癌和抗缺血活性。然而,三酮衍生物保护神经元细胞免受氧化应激诱导的细胞损伤的能力迄今尚未得到研究。作为一种具有潜在神经保护活性的高效抗氧化剂的持续努力,我们合成了β-雪松醇及其甲氧基类似物的 7-取代衍生物。取代基为杂环(哌嗪、吗啉)或杂芳环(三唑、吡啶)。只有β-雪松醇的哌嗪衍生物能够保护 HT22 海马神经元免受氧化应激诱导的细胞死亡。

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