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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
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    </authors>
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   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2023</year>
    <pub-dates>
     <date>2023-09-22</date>
    </pub-dates>
   </dates>
   <doi>10.1007/s11094-023-02832-1</doi>
   <abstract>Thietane-containing 4-(2-oxo-2-phenylethyl)-1H-1,2,4-triazol-4-ium bromides were synthesized by quaternization of thietanyltriazoles with phenacyl bromides. The starting thietanyltriazoles were obtained by the reaction of 1,2,4-triazoles and 2-chloromethylthiirane followed by oxidation of 1-(thietan-3-yl)-1,2,4-triazole to 1-(1-oxidotheitan-3-yl)-1,2,4-triazole and 1-(1,1-dioxidothietan-3-yl)-1,2,4-triazole. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C and 15N NMR spectroscopy. An in vivo study of the antidepressant activity revealed the promising compound 1-(1,1-dioxidothietan-3-yl)-4-(2-oxo-2-phenylethyl)-1H-1,2,4-triazol-4-ium bromide (IXa), which statistically significantly reduced the duration of immobilization in the forced swimming test by 44% as compared to the control group. Compound IXa is a low-toxic substance (class 4 toxicity) with a high bioavailability predicted according to in silico calculations. © 2023, Springer Science+Business Media, LLC, part of Springer Nature.</abstract>
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     <url>https://repo.bashgmu.ru/publication/2974</url>
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     <url>https://repo.bashgmu.ru/files/3150</url>
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