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Design and synthesis of thiophenone and furanthione butenolide bioisosteres with inhibitory activity towards acetylcholinesterase

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F22%3A00561033" target="_blank" >RIV/61388963:_____/22:00561033 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.molstruc.2022.133831" target="_blank" >https://doi.org/10.1016/j.molstruc.2022.133831</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.molstruc.2022.133831" target="_blank" >10.1016/j.molstruc.2022.133831</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Design and synthesis of thiophenone and furanthione butenolide bioisosteres with inhibitory activity towards acetylcholinesterase

  • Original language description

    A library of butenolide bioisosteres with sulfur incorporated in the molecule was synthetized and used for the structure-activity relationship studies associated with their inhibitory activity towards the AChE enzyme. Modifications through bioisosteric exchange of oxygen for sulfur either in position one of the butenolide ring (thiophenones) or on C2 (furanthiones) and further modification of the backbone via nucleophilic alkylation resulted in differential binding with the AChE enzyme. In general, the furanthiones were more efficient at binding AChE while some of the thiophenones were predicted to be toxic. Compound 11a, a C5 disubstituted furan-2(5H)-thione containing both the methyl and the isopropyl groups at C5 displayed the most encouraging inhibitory activity towards AChE. Molecular dynamics simulations in terms of the RMSD and RMSF trajectories and intermolecular bond analysis revealed considerable stability of the complex. Reactivity of 11a was further validated by quantum chemical calculations using DFT.

  • 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

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GA20-11571S" target="_blank" >GA20-11571S: Butenolides with neuroprotective effect from plant-derived smoke and their synthetic derivatives</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • 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 Molecular Structure

  • ISSN

    0022-2860

  • e-ISSN

    1872-8014

  • Volume of the periodical

    1269

  • Issue of the periodical within the volume

    December

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    133831

  • UT code for WoS article

    000877094300006

  • EID of the result in the Scopus database

    2-s2.0-85136657124