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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2021</year>
    <pub-dates>
     <date>2021-09-16</date>
    </pub-dates>
   </dates>
   <doi>10.1134/S1070363221070045</doi>
   <abstract>Abstract: The click reaction of propargylisatins with some azido-sugars was used to synthesize new isatin derivatives, in which the carbohydrate residue is linked to the 2,3-dioxindole scaffold via the 1,2,3-triazole ring. A number of water-soluble acylhydrazones with various structure of cationic fragment were obtained on their basis. It was shown that the newly obtained compounds do not exhibit hemotoxic action and have a significant antiaggregatory and anticoagulant activity at the level of reference drugs such as acetylsalicylic acid and pentoxifylline. [Figure not available: see fulltext.]. © 2021, Pleiades Publishing, Ltd.</abstract>
   <urls>
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     <url>https://repo.bashgmu.ru/publication/1660</url>
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    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/1831</url>
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