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• W2909800683 abstract "Abstract Four series of novel compounds based on 4‐aminopyridine, glatiramer acetate, pyrone, and coumarin backbones were sufficiently synthesized and identified by spectroscopic methods. CYP enzyme inhibition assays of five predominate human P450 isozymes indicate that all compounds, except for 4‐hydrazide pyridine 1c , seem to be less toxic than 4‐aminopyridine. Further investigation of the compounds using molecular docking experiments revealed different, the same, or stronger binding modes for most of the synthesized compounds, with both polar and hydrophobic interactions with the 1WDA and 1J95 receptors compared to benzoyl l ‐arginine amide and 4‐aminopyridine, respectively. These results introduce the synthesized compounds as K + channel blockers that could be considered for in vivo CNS disease studies." @default.
• W2909800683 created "2019-01-25" @default.
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• W2909800683 date "2019-01-14" @default.
• W2909800683 modified "2023-10-01" @default.
• W2909800683 title "Synthesis, CYP 450 evaluation, and docking simulation of novel 4-aminopyridine and coumarin derivatives" @default.
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• W2909800683 doi "https://doi.org/10.1002/ardp.201800247" @default.
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• W2909800683 hasPublicationYear "2019" @default.
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