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Esters and amides of hexanoic acids substituted with tertiary amino group in terminal position and their activity as transdermal permeation enhancers

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16370%2F10%3A00002650" target="_blank" >RIV/62157124:16370/10:00002650 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Esters and amides of hexanoic acids substituted with tertiary amino group in terminal position and their activity as transdermal permeation enhancers

  • Original language description

    Series of alkyl esters of 6-diethylamino-, 6-(pyrrolidin-1-yl)-, 6-(piperidin-1-yl) and 6-(morpholin-4-yl)hexanoic acids and alkylamides of 6-dimethylamino-, 6-(piperidin-1-yl) and 6-(morpholin-4-yl)hexanoic acids, containing 8 ? 12 carbon atoms in alkylchain, were prepared by methods of classical organic synthesis. The appropriate secondary amine was alkylated with ethyl-6-bromohexanoate to give ester of -substituted hexanoic acid, except of ethyl-6-dimethylaminohexanoate (1), which was prepared by Eschweiler-Clarke methylation of 6-aminohexanoic acid followed by direct esterification with ethanol. Resulted esters of -substituted hexanoic acids underwent direct transesterification with long chain alkanols to yield desired amino esters, or they were treated with long-chain alkylamines to prepare secondary amides of the appropriate heterocyclic hexanoic acids. These products were tested on their activity as transdermal permeation enhancers in vitro on the strips of the excised human sk

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2010

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Serbian Chemical Society

  • ISSN

    0352-5139

  • e-ISSN

  • Volume of the periodical

    75

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    CS - SERBIA AND MONTENEGRO

  • Number of pages

    9

  • Pages from-to

  • UT code for WoS article

    000278640900001

  • EID of the result in the Scopus database