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• W2593718300 startingPage "135" @default.
• W2593718300 abstract "A series of (1-(benzyl (aryl) amino) cyclohexyl) methyl esters 7a-n were prepared and screened for their anticonvulsant profile. Screening of these esters 7a-n and their starting alcohols 6a and 6b revealed that compound 7k was the most potent one in the scPTZ screening test with an ED50 value of 0.0056 mmol/kg being about 10- and 164-fold more potent than phenobarbital (ED50 = 0.056 mmol/kg) and ethosuximide (ED50 = 0.92 mmol/kg) as reference drugs, respectively. Meanwhile, in the MES test, compounds 7b and 7k at doses 0.0821 mmol/kg and 0.0334 mmol/kg, exerted 66% and 50% protection of the tested mice, respectively, compared with diphenylhydantoin, which exerted 100% protection at dose 0.16 mmol/kg. In the neurotoxicity screen test, almost all esters 7a-n did not show any minimal motor impairment at the maximum administrated dose. The anticonvulsant effectiveness of esters 7a-n was higher than their corresponding alcohols 6a and 6b. Compounds 7b and 7k exhibited pronounced anticonvulsant activity devoid of neurotoxicity in minimal motor impairment test and hepatotoxicity in the serum enzyme activity assay. 3D pharmacophore model using Discovery Studio 2.5 programs showed high fit value. The obtained experimental results of sc-PTZ activity of compounds 7a-n was consistent with the molecular modeling study." @default.
• W2593718300 created "2017-03-16" @default.
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• W2593718300 date "2017-04-01" @default.
• W2593718300 modified "2023-10-02" @default.
• W2593718300 title "Synthesis, molecular modeling studies and anticonvulsant activity of certain (1-(benzyl (aryl) amino) cyclohexyl) methyl esters" @default.
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• W2593718300 doi "https://doi.org/10.1016/j.bioorg.2017.01.021" @default.
• W2593718300 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28267983" @default.
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