Cytotoxic effect, spectroscopy, DFT, enzyme inhibition, and moleculer docking studies of some novel mesitylaminopropanols: Antidiabetic and anticholinergics and anticancer potentials

dc.contributor.authorKhalilov, Ali N.
dc.contributor.authorTuzun, Burak
dc.contributor.authorTaslimi, Parham
dc.contributor.authorTas, Ayca
dc.contributor.authorTuncbilek, Zuhal
dc.contributor.authorCakmak, Nese Keklikcioglu
dc.contributor.authorTaslimi, Parham
dc.date.accessioned2025-10-18T13:22:27Z
dc.date.created2021
dc.date.issued2021
dc.departmentFakülteler, Fen Fakültesi, Biyoteknoloji Bölümü
dc.description.abstractbeta-Amino alcohols (2-4) used in this study were re-synthesized in accordance with our previous study. All compounds were characterized by the combination of NMR, UV-Vis, IR experimental and theoretical spectral data. Then, the cytotoxic activity studies of the molecules on SH-SY5Y and L-929 cell lines showed that compound 2 has the highest activity on SH-SY5Y cells. Afterwards, the inhibition properties of these derivatives were tested toward acetylcholinesterase (AChE) and alpha-Glycosidase (alpha-Gly) enzymes. The studied molecules were optimized on B3LYP, HF, M062X level 3-21 g, 6-31 g, and SDD basis sets. Molecular docking calculations were made to determine the biological activity values of the amino alcohols against the enzymes. Finally, the drug properties of molecules were investigated by ADME/T analysis. (C) 2021 Elsevier B.V. All rights reserved.
dc.description.sponsorshipBaku State University [RGD-020]; Scientific Research Project Fund of Sivas Cumhuriyet University [RGD-020]
dc.description.sponsorshipThis work is supported by the Baku State University and Scientific Research Project Fund of Sivas Cumhuriyet University under the project number RGD-020. This research was made possible by TUBITAK ULAKBIM, High Performance and Grid Computing Center (TR-Grid e-Infrastructure).
dc.identifier.doi10.1016/j.molliq.2021.117761
dc.identifier.issn0167-7322
dc.identifier.issn1873-3166
dc.identifier.orcidTaslimi, Parham/0000-0002-3171-0633
dc.identifier.orcidTUZUN, BURAK/0000-0002-0420-2043;
dc.identifier.scopus2-s2.0-85117125944
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.molliq.2021.117761
dc.identifier.urihttps://hdl.handle.net/11772/22343
dc.identifier.volume344
dc.identifier.wosWOS:000708714300056
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of Molecular Liquids
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.sdgGoal-03: Good Health and Well-Being
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzWoS_20251016
dc.subjectBeta-Amino Alcohols
dc.subjectMtt
dc.subjectDft
dc.subjectMolecular Docking
dc.subjectEnzyme
dc.subjectCell Culture
dc.titleCytotoxic effect, spectroscopy, DFT, enzyme inhibition, and moleculer docking studies of some novel mesitylaminopropanols: Antidiabetic and anticholinergics and anticancer potentials
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationdadfa319-65b8-4543-92b4-bea49e0139e9
relation.isAuthorOfPublication.latestForDiscoverydadfa319-65b8-4543-92b4-bea49e0139e9

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