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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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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