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- W2105564434 abstract "The amine position of the K+ channel blocker 4-aminopyridine was functionalized to form amide, carbamate and urea derivatives in an attempt to identify novel compounds which restore conduction in injured spinal cord. Eight derivatives were tested in vitro, using a double sucrose gap chamber, for the ability to restore conduction in isolated, injured guinea pig spinal cord. The methyl, ethyl and t-butyl carbamates of 4-aminopyridine induced an increase in the post injury compound action potential. The methyl and ethyl carbamates were further tested in an in vivo model of spinal cord injury. These results represent the first time that 4-aminopyridine has been derivatized without losing its ability to restore function in injured spinal cord tissue." @default.
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- W2105564434 date "2005-09-01" @default.
- W2105564434 modified "2023-09-23" @default.
- W2105564434 title "Development of novel 4-aminopyridine derivatives as potential treatments for neurological injury and disease" @default.
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- W2105564434 doi "https://doi.org/10.1016/j.ejmech.2005.04.017" @default.
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