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Profiling donepezil template into multipotent hybrids with antioxidant properties

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18470%2F18%3A50014446" target="_blank" >RIV/62690094:18470/18:50014446 - isvavai.cz</a>

  • Alternative codes found

    RIV/60162694:G44__/18:43889471 RIV/00023752:_____/18:43919338 RIV/00179906:_____/18:10373702

  • Result on the web

    <a href="https://www.ncbi.nlm.nih.gov/pubmed/29529892" target="_blank" >https://www.ncbi.nlm.nih.gov/pubmed/29529892</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1080/14756366.2018.1443326" target="_blank" >10.1080/14756366.2018.1443326</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Profiling donepezil template into multipotent hybrids with antioxidant properties

  • Original language description

    Alzheimer&apos;s disease is debilitating neurodegenerative disorder in the elderly. Current therapy relies on administration of acetylcholinesterase inhibitors (AChEIs) -donepezil, rivastigmine, galantamine, and N-methyl-d-aspartate receptor antagonist memantine. However, their therapeutic effect is only short-term and stabilizes cognitive functions for up to 2 years. Given this drawback together with other pathological hallmarks of the disease taken into consideration, novel approaches have recently emerged to better cope with AD onset or its progression. One such strategy implies broadening the biological profile of AChEIs into so-called multi-target directed ligands (MTDLs). In this review article, we made comprehensive literature survey emphasising on donepezil template which was structurally converted into plethora of MTLDs preserving anti-cholinesterase effect and, at the same time, escalating the anti-oxidant potential, which was reported as a crucial role in the pathogenesis of the Alzheimer&apos;s disease. [GRAPHICS] .

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30107 - Medicinal chemistry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • 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 enzyme inhibition and medicinal chemistry

  • ISSN

    1475-6366

  • e-ISSN

  • Volume of the periodical

    33

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    24

  • Pages from-to

    583-606

  • UT code for WoS article

    000427559100001

  • EID of the result in the Scopus database