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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Кондратенко, Р.М.</author>
     <author>Балтина, Л.А.</author>
     <author>Исмагилова, А.Ф.</author>
     <author>Васильева, Е.В.</author>
     <author>Насыров, Х.М.</author>
     <author>Толстиков, Г.А.</author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
     <author></author>
    </authors>
   </contributors>
   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2001</year>
    <pub-dates>
     <date>2018-01-23</date>
    </pub-dates>
   </dates>
   <abstract>Typically possessing low toxicity and a broad spectrum&#13;
of biological activity, plant triterpenoids are valuable raw&#13;
materials for the creation of new drugs [1 – 4]. Of special interest&#13;
in this respect are the major triterpenoids contained in&#13;
the root extract obtained from plants of the common licorice&#13;
(Glycyrrhiza glabra L.) and Ural licorice (Glycyrrhiza&#13;
uralensis Fisher ) species. These substances are represented&#13;
by 18 -glycyrrhetic acid (I) and its modified analogs, which&#13;
serve as the base for effective antiinflammatory, antiallergic,&#13;
and antiulcer preparations [2, 5 – 9]. The antiulcer drugs include&#13;
the sodium salt of acid I (glycyrrhenate sodium) [2]&#13;
and the disodium salt of acid I succinate (carbenoxolone, II)</abstract>
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     <url>https://repo.bashgmu.ru/files/685</url>
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