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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors/>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2022</year>
    <pub-dates>
     <date>2022-04-05</date>
    </pub-dates>
   </dates>
   <doi>10.5599/admet.1179</doi>
   <abstract>A series of biorelevant triethylammonium isatin hydrazones containing various substituents in the aromatic fragment have been synthesized. Their structure and composition were confirmed by NMR-and IR-spectroscopies, mass-spectrometry and elemental analysis. It was found that some representatives show activity against Staphylococcus aureus and Bacillus cereus higher or at the level of norfloxacin, including methicillin-resistant Staphylococcus aureus strains. The study also showed low hemo-and cytotoxicity (Chang Liver) and high antiaggregatory and anticoagulant activity of these compounds. The high potential of new ammonium isatin-3-acylhydrazones in the search for antimicrobial activity against phytopathogens of bacterial and fungal nature has been shown for the first time. (C) 2021 by the authors.</abstract>
   <urls>
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     <url>https://repo.bashgmu.ru/publication/2511</url>
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    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/2687</url>
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