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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">vestich</journal-id><journal-title-group><journal-title xml:lang="ru">Известия Национальной академии наук Беларуси. Серия химических наук</journal-title><trans-title-group xml:lang="en"><trans-title>Proceedings of the National Academy of Sciences of Belarus, Chemical Series</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1561-8331</issn><issn pub-type="epub">2524-2342</issn><publisher><publisher-name>The Republican Unitary Enterprise Publishing House "Belaruskaya Navuka"</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">vestich-183</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>Статьи</subject></subj-group></article-categories><title-group><article-title>Дизайн, синтез и биологические свойства ингибиторов ВСR-ABL тирозинкиназы, применяемых для лечения хронического миелолейкоза</article-title><trans-title-group xml:lang="en"><trans-title>Design, synthesis and biological properties of BCR-ABL tyrosine kinase inhibitors used for chronic myelogenous leucemia treatment</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>Фарина</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Farina</surname><given-names>A. V.</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>Калиниченко</surname><given-names>Е. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Kalinichenko</surname><given-names>E. N.</given-names></name></name-alternatives><email xlink:type="simple">kalinichenko@iboch.bas-net.by</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт биоорганической химии НАН Беларуси</institution></aff><aff xml:lang="en"><institution>Institute of Bioorganic Chemistry of the National Academy of Sciences of Belarus</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>08</day><month>06</month><year>2016</year></pub-date><volume>0</volume><issue>1</issue><fpage>105</fpage><lpage>121</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Фарина А.В., Калиниченко Е.Н., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Фарина А.В., Калиниченко Е.Н.</copyright-holder><copyright-holder xml:lang="en">Farina A.V., Kalinichenko E.N.</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://vestichem.belnauka.by/jour/article/view/183">https://vestichem.belnauka.by/jour/article/view/183</self-uri><abstract><p>Эффективность лечения хронического миелолейкоза существенно повысилась после введения в клиническую практику иматиниба - селективного ингибитора BCR-ABL тирозинкиназы. Описаны история разработки иматиниба, методы его синтеза и направления дальнейшей оптимизации структуры.</p></abstract><trans-abstract xml:lang="en"><p>Imatinib, a selective BCR-ABL tyrosine kinase inhibitor has significantly improved efficacy of chronic myelogenous leukemia treatment. This review focuses on discovery and development of imatinib, methods of its synthesis and further structure optimization opportunities.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>иматиниб</kwd><kwd>ингибиторы тирозинкиназы</kwd><kwd>хронический миелоидный лейкоз</kwd><kwd>imatinib</kwd><kwd>tyrosine kinase inhibitors</kwd><kwd>chronic myelogenous leukemia</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">Fialkow, P. J. Chronic myelocytic leukemia: clonal origin in a stem cell common to the granulocyte, erythrocyte, platelet and monocyte/macrophage / P. J. Fialkow, R. J. Jacobson, T. 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