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咪唑-1-乙基吲唑电压门控钠离子通道配体在多发性硬化症小鼠模型的视神经炎中具有神经保护作用。

Imidazol-1-ylethylindazole voltage-gated sodium channel ligands are neuroprotective during optic neuritis in a mouse model of multiple sclerosis.

机构信息

Biological and Medicinal Chemistry, Wolfson Institute for Biomedical Science, University College London , Gower Street, London WC1E 6BT, United Kingdom.

出版信息

J Med Chem. 2014 Apr 10;57(7):2942-52. doi: 10.1021/jm401881q. Epub 2014 Mar 21.

Abstract

A series of imidazol-1-ylethylindazole sodium channel ligands were developed and optimized for sodium channel inhibition and in vitro neuroprotective activity. The molecules exhibited displacement of a radiolabeled sodium channel ligand and selectivity for blockade of the inactivated state of cloned neuronal Nav channels. Metabolically stable analogue 6 was able to protect retinal ganglion cells during optic neuritis in a mouse model of multiple sclerosis.

摘要

一系列咪唑-1-乙基吲唑钠离子通道配体被开发和优化,以实现钠离子通道抑制和体外神经保护活性。这些分子表现出对放射性标记的钠离子通道配体的置换作用,并对克隆神经元 Nav 通道的失活状态具有选择性阻断作用。代谢稳定的类似物 6 能够在多发性硬化症的小鼠模型中保护视神经炎期间的视网膜神经节细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0158/4010550/ad98a8869e33/jm-2013-01881q_0002.jpg

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