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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Meshcheryakova, S.A.</author>
     <author>Kataev, V.A.</author>
     <author>Nikolaeva, K.V.</author>
     <author>Perfilova, V.N.</author>
     <author>Borodin, D.D.</author>
     <author>Tyurenkov, I.N.</author>
    </authors>
   </contributors>
   <titles>
    <title>SYNTHESIS, ISOMERISM, AND HYPOTENSIVE ACTIVITY OF THIETHANE-CONTAINING HYDRAZONES OF URACILYLACETIC ACID</title>
   </titles>
   <dates>
    <year>2014</year>
    <pub-dates>
     <date>2018-10-03</date>
    </pub-dates>
   </dates>
   <abstract>By the reaction of 2-[6-methyl-1-(thiethane-3-yl)uracil-3-yl]acetic acid hydrazide with aryl aldehydes and acetophenone derivatives, acylhydrazones have been obtained, which exist in DMSO solutions as a mixture of two stereoisomers of an EC=N-isomer, due to the hindered internal rotation around the hydrazide bond. It has been found that the compounds synthesized exhibit a hypotensive activity. © 2014 Pleiades Publishing, Ltd.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/645</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/719</url>
    </pdf-urls>
   </urls>
  </record>
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