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本文引用的文献

1
Synthesis and study of new paramagnetic and diamagnetic verapamil derivatives.合成与研究新的顺磁和反磁维拉帕米衍生物。
Bioorg Med Chem. 2010 Apr 15;18(8):2954-63. doi: 10.1016/j.bmc.2010.02.040. Epub 2010 Feb 25.
2
Mechanisms underlying inflammation in neurodegeneration.神经变性中炎症的发生机制。
Cell. 2010 Mar 19;140(6):918-34. doi: 10.1016/j.cell.2010.02.016.
3
Fibrillar oligomers nucleate the oligomerization of monomeric amyloid beta but do not seed fibril formation.纤维状寡聚物启动单体淀粉样β的寡聚化,但不引发纤维形成。
J Biol Chem. 2010 Feb 26;285(9):6071-9. doi: 10.1074/jbc.M109.069542. Epub 2009 Dec 15.
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Alzheimer's disease: from pathology to therapeutic approaches.阿尔茨海默病:从病理学到治疗方法
Angew Chem Int Ed Engl. 2009;48(17):3030-59. doi: 10.1002/anie.200802808.
5
Candidate anti-A beta fluorene compounds selected from analogs of amyloid imaging agents.从淀粉样蛋白成像剂类似物中筛选出候选抗 Aβ 芴类化合物。
Neurobiol Aging. 2010 Oct;31(10):1690-9. doi: 10.1016/j.neurobiolaging.2008.09.019. Epub 2008 Nov 20.
6
Nitric oxide and nitroxides can act as efficient scavengers of protein-derived free radicals.一氧化氮和氮氧化物可作为蛋白质衍生自由基的有效清除剂。
Chem Res Toxicol. 2008 Nov;21(11):2111-9. doi: 10.1021/tx800183t.
7
Reversible reduction of nitroxides to hydroxylamines: roles for ascorbate and glutathione.氮氧化物可逆还原为羟胺:抗坏血酸和谷胱甘肽的作用
Free Radic Biol Med. 2007 Feb 1;42(3):404-12. doi: 10.1016/j.freeradbiomed.2006.11.007. Epub 2006 Nov 10.
8
Exploring interaction of beta-amyloid segment (25-35) with membrane models through paramagnetic probes.通过顺磁探针探索β-淀粉样蛋白片段(25-35)与膜模型的相互作用。
J Pept Sci. 2006 Dec;12(12):766-74. doi: 10.1002/psc.811.
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Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases.神经退行性疾病中的线粒体功能障碍与氧化应激
Nature. 2006 Oct 19;443(7113):787-95. doi: 10.1038/nature05292.
10
Inhibitory activity of stilbenes on Alzheimer's beta-amyloid fibrils in vitro.芪类化合物对阿尔茨海默病β-淀粉样蛋白原纤维的体外抑制活性。
Bioorg Med Chem. 2007 Jan 15;15(2):1160-7. doi: 10.1016/j.bmc.2006.09.069. Epub 2006 Oct 1.

氮氧自由基修饰的 2-氨基-7-溴芴的合成与研究及其前体作为双重抗淀粉样蛋白和抗氧化活性化合物。

Synthesis and study of 2-amino-7-bromofluorenes modified with nitroxides and their precursors as dual anti-amyloid and antioxidant active compounds.

机构信息

Institute of Organic and Medicinal Chemistry, University of Pécs, Szigeti st 12, H-7624 Pécs, Hungary.

出版信息

Eur J Med Chem. 2011 Apr;46(4):1348-55. doi: 10.1016/j.ejmech.2011.01.059. Epub 2011 Feb 3.

DOI:10.1016/j.ejmech.2011.01.059
PMID:21333407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3650846/
Abstract

A series of 2-aminofluorenes N-alkylated with nitroxides or their precursors were synthesized. The new compounds were tested on hydroxyl radical and peroxyl radical scavenging ability and inflammatory assay on the endothelial brain cells. In agreement with ROS scavenging ability the same compound 7-bromo-N -[(1-Oxyl-2,2,6,6-tetramethyl-1,2,3,6-tetrahydropyridine-4yl)methyl]-9H-fluoren-2-amine (3b) and its hydroxylamine salt (3b/OH/HCl) showed the anti-inflammatory property on the endothelial brain cells.

摘要

合成了一系列被氮氧自由基或其前体烷化的 2-氨基芴。新化合物的羟基自由基和过氧自由基清除能力以及对内皮脑细胞的炎症反应进行了测试。与 ROS 清除能力一致,相同的化合物 7-溴-N -[(1-氧代-2,2,6,6-四甲基-1,2,3,6-四氢吡啶-4-基)甲基]-9H-芴-2-胺(3b)及其羟胺盐(3b/OH/HCl)在对内皮脑细胞显示出抗炎特性。