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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">10.37489/2587-7836-2022-2-03-10</article-id><article-id custom-type="elpub" pub-id-type="custom">phkinetica-312</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 2. Блокаторы HCN-каналов</article-title><trans-title-group xml:lang="en"><trans-title>Сardioprotective agents with biaromatic structure. Part 2. HCN channel 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. SPIN-код: 8755-7666</p><p>Москва</p></bio><bio xml:lang="en"><p>Mokrov Grigory V., PhD Chemical Sci., Leading researcher of the fine organic synthesis laboratory at the drug chemistry department. SPIN code: 8755-7666</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>2022</year></pub-date><pub-date pub-type="epub"><day>06</day><month>07</month><year>2022</year></pub-date><volume>0</volume><issue>2</issue><fpage>3</fpage><lpage>10</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Мокров Г.В., 2022</copyright-statement><copyright-year>2022</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/312">https://www.pharmacokinetica.ru/jour/article/view/312</self-uri><abstract><p>Управляемые циклическими нуклеотидами гиперполяризационно-активируемые каналы (HCN-каналы), прежде всего, их HCN4-подтип, являются одной из перспективных мишеней для разработки кардиопротекторных средств. Блокаторы HCN-каналов обладают селективным брадикардическим действием, сохраняя сократимость миокарда и диастолическую функцию и не оказывая влияния на электрофизиологические параметры сердца. Настоящий обзор продолжает серию обзоров по анализу соединений с кардиопротекторными свойствами в ряду биароматических структур, к которым относится и широкий ряд блокаторов HCN-каналов.</p></abstract><trans-abstract xml:lang="en"><p>Hyperpolarization-activated cyclic nucleotide–gated (HCN) channels, primarily their HCN4 subtype, are one of the promising targets for the development of cardioprotective agents. HCN channel blockers have a selective bradycardic effect, preserving myocardial contractility and diastolic function and not affecting the electrophysiological parameters of the heart. This review continues a series of reviews on the analysis of compounds with cardioprotective properties in a number of biaromatic structures, which include a wide range of HCN channel blockers.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>антиаритмики</kwd><kwd>кардиопротекторы</kwd><kwd>блокаторы HCN-каналов</kwd><kwd>биароматические соединения</kwd></kwd-group><kwd-group xml:lang="en"><kwd>antiarrhythmics</kwd><kwd>cardioprotectors</kwd><kwd>HCN-channels 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">Postea O, Biel M. Exploring HCN channels as novel drug targets. Nat Rev Drug Discov. 2011;10(12):903–914. DOI: 10.1038/NRD3576.</mixed-citation><mixed-citation xml:lang="en">Postea O, Biel M. Exploring HCN channels as novel drug targets. Nat Rev Drug Discov. 2011;10(12):903–914. 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