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Estimating the lipophilicity of a number of 2-amino-1-cyclohexanol derivatives exhibiting anticonvulsant activity

✍ Scribed by Elżbieta Pękala; Henryk Marona


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
134 KB
Volume
23
Category
Article
ISSN
0269-3879

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✦ Synopsis


Abstract

The lipophilicity of a number of N‐acyl derivatives of trans‐ or cis‐: racemic, (1__R__,2__R__)‐ or (1__S__,2__S__)‐aminocyclohexanol (1–13) exhibiting anticonvulsant activity was investigated. Their lipophilicity (R~m0~) was determined using reversed‐phase thin‐layer chromatography (RP‐TLC) with mixtures of methanol and water as mobile phases. The partition coefficients of compounds 1–13 (log P) were also calculated using two computer programs (Pallas and Chem DU) and compared with R~m0~. Copyright © 2009 John Wiley & Sons, Ltd.


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