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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">pharmjournal</journal-id><journal-title-group><journal-title xml:lang="ru">Разработка и регистрация лекарственных средств</journal-title><trans-title-group xml:lang="en"><trans-title>Drug development &amp; registration</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2305-2066</issn><issn pub-type="epub">2658-5049</issn><publisher><publisher-name>LLC «CPHA»</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">pharmjournal-429</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>АНАЛИТИЧЕСКИЕ МЕТОДИКИ И МЕТОДЫ КОНТРОЛЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ANALYTICAL AND QUALITY CONTROL METHODS</subject></subj-group></article-categories><title-group><article-title>СИНТЕЗ, ФИЗИКО-ХИМИЧЕСКИЙ АНАЛИЗ И ФАРМАКОЛОГИЧЕСКАЯ АКТИВНОСТЬ НЕКОТОРЫХ ПРОИЗВОДНЫХ ВАРФАРИНА</article-title><trans-title-group xml:lang="en"><trans-title>SYNTHESIS, PHYSICO-CHEMICAL ANALYSIS AND PHARMACOLOGICAL ACTIVITY OF SOME DERIVATIVES OF WARFARIN</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Абышев</surname><given-names>А. З.</given-names></name><name name-style="western" xml:lang="en"><surname>Abyshev</surname><given-names>A. Z.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Журкович</surname><given-names>И. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Zhurkovich</surname><given-names>I. K.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ивкин</surname><given-names>Д. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivkin</surname><given-names>D. Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нгуен</surname><given-names>К. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Nguyen</surname><given-names>C. B.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Санкт-Петербургская государственная химико-фармацевтическая академия» Министерства здравоохранения Российской Федерации</institution></aff><aff xml:lang="en"><institution>Saint-Petersburg State Chemical-Pharmaceutical Academy, Ministry of Healthcare</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБУН «Институт токсикологии ФМБА»</institution></aff><aff xml:lang="en"><institution>Institute of Toxicology FMBA</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>09</day><month>01</month><year>2019</year></pub-date><volume>0</volume><issue>2</issue><fpage>192</fpage><lpage>198</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Абышев А.З., Журкович И.К., Ивкин Д.Ю., Нгуен К.Б., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Абышев А.З., Журкович И.К., Ивкин Д.Ю., Нгуен К.Б.</copyright-holder><copyright-holder xml:lang="en">Abyshev A.Z., Zhurkovich I.K., Ivkin D.Y., Nguyen C.B.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.pharmjournal.ru/jour/article/view/429">https://www.pharmjournal.ru/jour/article/view/429</self-uri><abstract><p>Разработаны методы синтеза 7 производных варфарина, из которых три являются комбинированными. Современными спектральными методами (ИК-, ЯМР-спектроскопия) определены их структурные особенности, физико-химические свойства синтезированных соединений. Изучена их антикоагулянтная активность in vivo путем определения протромбинового времени (ПТВ). Наиболее выраженной активностью, сравнимой с препаратом варфарином (37,4±2,8 с), обладали субстанции AZ-5 (конъюгат варфарина с фрагментом субстанции диуманкала, 41,2±2,3 с) и AZ-9 (диуманкал, 45,18±4,85 с), сравнимые с препаратом варфарином (37,4±2,8 с).</p></abstract><trans-abstract xml:lang="en"><p>Methods of synthesis of 7 warfarin derivatives from which three are combined has been developed. Their structural features, physicochemical properties of synthesized compounds by modern and spectral methods (IR, NMR spectroscopy) were determined. Their anticoagulant activity in vivo were studied by determining prothrombin time (PT). The most pronounced activity was possessed by substances AZ-5 (conjugate warfarin with a fragment of the substance diumancal, 41,2±2,3 s) and AZ-9 (diumancal, 45,18±4,85 s), comparable with the reference drug warfarin (37,4±2,8 s).</p></trans-abstract><kwd-group xml:lang="ru"><kwd>кумарин</kwd><kwd>варфарин</kwd><kwd>диуманкал</kwd><kwd>антикоагулянтная активность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>coumarin</kwd><kwd>warfarin</kwd><kwd>diumancal</kwd><kwd>anticoagulant activity</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">А.З. Абышев, Э.М. Агаев, Р.А. Абышев. Природные и синтетические кумарины и флавоноиды. - Баку: Наука и образование, 2014. 482 с.</mixed-citation><mixed-citation xml:lang="en">А.З. Абышев, Э.М. Агаев, Р.А. Абышев. 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