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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">phkinetica</journal-id><journal-title-group><journal-title xml:lang="ru">Фармакокинетика и Фармакодинамика</journal-title><trans-title-group xml:lang="en"><trans-title>Pharmacokinetics and Pharmacodynamics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2587-7836</issn><issn pub-type="epub">2686-8830</issn><publisher><publisher-name>ООО «Издательство ОКИ»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.37489/2587-7836-2023-3-3-11</article-id><article-id custom-type="elpub" pub-id-type="custom">phkinetica-376</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>АКТУАЛЬНЫЕ ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CURRENT REVIEWS</subject></subj-group></article-categories><title-group><article-title>Кардиопротекторные средства с биароматической структурой. Часть 6. Бета-блокаторы</article-title><trans-title-group xml:lang="en"><trans-title>Сardioprotective agents with biaromatic structure. Part 6. Beta blockers</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2617-0334</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мокров</surname><given-names>Г. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Mokrov</surname><given-names>G. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мокров Григорий Владимирович - к. х. н., в. н. с. лаборатории тонкого органического синтеза отдела химии лекарственных средств</p><p>Москва</p></bio><bio xml:lang="en"><p>Grigory V. Mokrov - PhD, Cand. Chemical Sci., Leading researcher of the fine organic synthesis laboratory at the drug chemistry department</p><p>Moscow</p></bio><email xlink:type="simple">g.mokrov@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «НИИ фармакологии имени В.В. Закусова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>FSBI “Zakusov Institute of Pharmacology”</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>02</day><month>11</month><year>2023</year></pub-date><volume>0</volume><issue>3</issue><fpage>3</fpage><lpage>11</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Мокров Г.В., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Мокров Г.В.</copyright-holder><copyright-holder xml:lang="en">Mokrov G.V.</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.pharmacokinetica.ru/jour/article/view/376">https://www.pharmacokinetica.ru/jour/article/view/376</self-uri><abstract><p>β-Адреноблокаторы — один из старейших классов кардиопротекторов, применяемых при лечении сердечно-сосудистых заболеваний. Они уменьшают частоту сердечных сокращений, имеют гипотензивное действие, угнетают сократимость миокарда и обладают антиаритмическими свойствами. В ряду биароматических соединений с линейным линкером имеется достаточно обширная группа β-блокаторов, которые помимо двух ароматических ядер содержат в линкере 1,2-дигидрокси-3-аминопропановый фрагмент — ключевой для наличия β-блокирующей активности. Среди соединений этой группы имеются широко применяемые препараты небиволол и карведилол, которые используются при терапии хронической сердечной недостаточности и артериальной гипертензии.</p></abstract><trans-abstract xml:lang="en"><p>β-Blockers are one of the oldest classes of cardioprotectors used in the treatment of cardiovascular diseases. They reduce the heart rate, have a hypotensive eﬀect, inhibit myocardial contractility and have antiarrhythmic properties. In the series of biaromatic compounds with a linear linker, there is a quite large group of β-blockers, which in addition to two aromatic nuclei contain a 1,2-dihydroxy-3-aminopropane fragment in the linker, that is the key for the presence of β-blocking activity. Among the compounds of this group are widely used drugs nebivolol and carvedilol, which are used in the treatment of chronic heart failure and arterial hypertension.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>антиаритмики</kwd><kwd>кардиопротекторы</kwd><kwd>блокаторы β-адренорецепторов</kwd><kwd>биароматические соединения</kwd></kwd-group><kwd-group xml:lang="en"><kwd>antiarrhythmics</kwd><kwd>cardioprotectors</kwd><kwd>β-adrenoreceptors blockers</kwd><kwd>biaromatic compounds</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">Fisker FY, Grimm D, Wehland M. 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