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Synthesis, structure, and cholinergic effect of novel neuroprotective compounds bearing the tacrine pharmacophore

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3AG44__%2F08%3A00001931" target="_blank" >RIV/60162694:G44__/08:00001931 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22310/08:00021410

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis, structure, and cholinergic effect of novel neuroprotective compounds bearing the tacrine pharmacophore

  • Original language description

    Novel tacrine congeners with side ligands suitable for optimal interaction with the peripheral and catalytic sites of acetyl- and butyrylcholinesterase (AChE and BuChE) have been synthesized using synthons 9-isothiocyanato-1,2,3,4-tetrahyhroacridine and9-chloro-1,2,3,4-tetrahydroacridine which represent convenient starting points for the synthesis by reaction with various substituted amines. The synthesized compounds were tested for their ability to inhibit AChE and BuChE whereby it was found that morpholine derivative 10c and furfuryl derivative 10b were the most potent AChE and BuChE inhibitors, respectively, with the latter compound comparable in activity to Tacrine.

  • Czech name

    Syntéza, struktura, a cholinergní efekt nových neuroprotektivních sloučenin nesoucích takrinový farmakofor

  • Czech description

    Nové takrinové obdoby s bočními ligandy vhodými pro optimální interakci s periferními a katalytickými částmi acetyl a butyrylcholinesterasy (AChE a BuChE) byly syntetizovány užitím syntonů 9-isothiocyanato-1,2,3,4-tatrahydroacridinu a 9-chloro-1,2,3,4-tetrahydroacridinu, které reprezentují vhodné počáteční body pro syntézu reakcí s rozličnými substituovanými aminy. Syntetizované sloučeniny byla testovány pro svou schopnost inhibovat AChE a BuChE přčemž bylo zjištěno, že morfolinový derivát 10c a furfuryl deriváty 10b byly nejúčinnější AChE a BuChE inhibitory.

Classification

  • Type

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

  • CEP classification

    FP - Other medical fields

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2008

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Heterocycles

  • ISSN

    0385-5414

  • e-ISSN

  • Volume of the periodical

    76

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    17

  • Pages from-to

  • UT code for WoS article

    000262427000032

  • EID of the result in the Scopus database