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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 pub-id-type="doi">10.29235/1561-8331-2021-57-3-356-384</article-id><article-id custom-type="elpub" pub-id-type="custom">vestich-672</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>ОБЗОРЫ</subject></subj-group></article-categories><title-group><article-title>Химическая модификация различных соединений азотсодержащими гетероциклами</article-title><trans-title-group xml:lang="en"><trans-title>Chemical modification of different compounds with nitrogen-containing heterocycles</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>Акишина</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Akishina</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Акишина Екатерина Александровна – аспирант, мл. науч. сотрудник</p><p>ул. Сурганова, 13, 220072, Минск</p></bio><bio xml:lang="en"><p>Ekaterina A. Akishina – Postgraduate student, Junior Researcher</p><p>13, Surganov Str., 220072, Minsk </p></bio><email xlink:type="simple">che.semenovaea@mail.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>Дикусар</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Dikusar</surname><given-names>Е. А.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дикусар Евгений Анатольевич – канд. хим. наук, ст. науч. сотрудник</p><p>ул. Сурганова, 13, 220072, Минск</p></bio><bio xml:lang="en"><p>Evgenij A. Dikusar – Ph. D. (Chemistry), Senior Researcher</p><p>13, Surganov Str., 220072, Minsk </p></bio><email xlink:type="simple">dikusar@ifoch.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 физико-органической химии Национальной академии наук Беларуси</institution></aff><aff xml:lang="en"><institution>Institute of Physical Organic Chemistry of the National Academy of Sciences of Belarus</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>05</day><month>09</month><year>2021</year></pub-date><volume>57</volume><issue>3</issue><fpage>356</fpage><lpage>384</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Акишина Е.А., Дикусар Е.А., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Акишина Е.А., Дикусар Е.А.</copyright-holder><copyright-holder xml:lang="en">Akishina E.A., Dikusar Е.А.</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/672">https://vestichem.belnauka.by/jour/article/view/672</self-uri><abstract><p>Соединения гетероциклического ряда имеют исключительно важное практическое значение, так как многие гетероциклы лежат в основе молекул ценнейших лекарственных веществ как природных (витамины, ферменты, алкалоиды и др.), так и синтетических биологически активных соединений. В работе в основном рассмотрены наиболее актуальные за последние 10 лет направления поиска лекарственных средств различного назначения путем модификации известных биоактивных природных, элементоорганических и каркасных соединений 1,2-азольным, оксазольным, оксадиазольным, тиазольным, триазольным, пиридиновым, пиримидиновым гетероциклами. Химическая модификация позволяет повысить водорастворимость соединений, что является важным при выборе путей наиболее рационального введения препарата в организм, уменьшить токсичность соответствующих веществ, увеличить широту терапевтического действия, а также придать веществам новые ценные лечебные свойства, что таким образом в значительной мере расширить их применение в медицине и сельском хозяйстве.</p></abstract><trans-abstract xml:lang="en"><p>Heterocyclic compounds have an extremely important practical application, since many heterocycles are the basis of the most valuable medicinal substances, both natural (vitamins, enzymes, alkaloids, etc.) and synthetic biologically active compounds. The work mainly considers the most relevant directions for various purposes drugs search by modifying known bioactive natural, organoelement and framework compounds with 1,2-azole, oxazole, oxadiazole, thiazole, triazole, pyridine, pyrimidine heterocycles over the past 10 years. Chemical modification makes it possible to increase the water solubility of the compounds, which is important when choosing the pathways for the most rational drug introduction into the body, to reduce the toxicity of the corresponding substances, to increase the breadth of the therapeutic action, and also to give new valuable medicinal properties, thus significantly expanding their application in medicine and agriculture.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>1</kwd><kwd>2-азолы</kwd><kwd>оксазол</kwd><kwd>оксадиазол</kwd><kwd>тиазол</kwd><kwd>триазол</kwd><kwd>пиридин</kwd><kwd>пиримидин</kwd><kwd>куркумин</kwd><kwd>ванилин</kwd><kwd>хитозан</kwd><kwd>стероиды</kwd><kwd>карборан</kwd><kwd>ферроцен</kwd><kwd>адамантан</kwd></kwd-group><kwd-group xml:lang="en"><kwd>1</kwd><kwd>2-azoles</kwd><kwd>oxazole</kwd><kwd>oxadiazole</kwd><kwd>thiazole</kwd><kwd>triazole</kwd><kwd>pyridine</kwd><kwd>pyrimidine</kwd><kwd>curcumin</kwd><kwd>vanillin</kwd><kwd>chitosan</kwd><kwd>steroids</kwd><kwd>carborane</kwd><kwd>ferrocene</kwd><kwd>adamantane</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">Lahlou, M. 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