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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 custom-type="elpub" pub-id-type="custom">phkinetica-176</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>ПОИСК НОВЫХ ФАРМАКОЛОГИЧЕСКИ АКТИВНЫХ СОЕДИНЕНИЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>SCREENING FOR NEW PHARMACOLOGICALLY ACTIVE COMPOUNDS</subject></subj-group></article-categories><title-group><article-title>Поиск селективных блокаторов цинк-зависимых металлопротеиназ 2-го и 9-го типа в ряду бензоиламино(фенилсульфонил)-замещенных циклических аминокислот</article-title><trans-title-group xml:lang="en"><trans-title>Search selective blockers of the zinc-dependent metalloproteinases 2nd and 9th type among the benzoylamino (phenylsulfonyl) amino-substituted cyclic aminoacids derivatives</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>Крыжановский</surname><given-names>С. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kryzhanovskii</surname><given-names>S. A.</given-names></name></name-alternatives><email xlink:type="simple">SAK-538@yandex.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>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><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>Григоркевич</surname><given-names>О. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Grigorkevich</surname><given-names>O. S.</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>Цорин</surname><given-names>И. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Tsorin</surname><given-names>I. B.</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>Столярук</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Stolyaruk</surname><given-names>V. N.</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>Вититнова</surname><given-names>М. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Vititnova</surname><given-names>M. B.</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>Лихошерстов</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Likhosherstov</surname><given-names>A. M.</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>Гудашева</surname><given-names>Т. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Gudasheva</surname><given-names>T. A.</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>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>2016</year></pub-date><pub-date pub-type="epub"><day>09</day><month>09</month><year>2016</year></pub-date><volume>0</volume><issue>3</issue><fpage>3</fpage><lpage>8</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Крыжановский С.А., Мокров Г.В., Григоркевич О.С., Цорин И.Б., Столярук В.Н., Вититнова М.Б., Лихошерстов А.М., Гудашева Т.А., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Крыжановский С.А., Мокров Г.В., Григоркевич О.С., Цорин И.Б., Столярук В.Н., Вититнова М.Б., Лихошерстов А.М., Гудашева Т.А.</copyright-holder><copyright-holder xml:lang="en">Kryzhanovskii S.A., Mokrov G.V., Grigorkevich O.S., Tsorin I.B., Stolyaruk V.N., Vititnova M.B., Likhosherstov A.M., Gudasheva T.A.</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/176">https://www.pharmacokinetica.ru/jour/article/view/176</self-uri><abstract><p>Цель настоящего исследования - поиск в ряду бензоиламино(фенилсульфонил)-замещённых циклических аминокислот биологически активных соединений, обладающих свойствами блокаторов, цинк-зависимых металлопротеиназ 2-го и 9-го типа, которые, как известно, играют ключевую роль в патогенезе раннего постинфарктного ремоделирования миокарда. При изучении влияния вновь синтезированных соединений на уровень экспрессии металлопротеиназы-9 в крови крыс с острым инфарктом миокарда было отобрано соединение-лидер - 1-({4-[(4-хлорбензоил) амино]фенил}сульфонил-1_-пролин, - которое эффективно блокирует повышения уровня этого фермента в крови. При помощи эхокардиографии показано, что отобранное соединение-лидер по своей способности препятствовать развитию ремоделирования миокарда в острейшую фазу экспериментального инфаркта миокарда, как минимум, не уступает эталонному ингибитору металлопротеиназ - доксициклину.</p></abstract><trans-abstract xml:lang="en"><p>The purpose of this study - search among the benzoylamino (phenyLsuLfonyL) amino-substituted cyclic aminoacids derivatives biologically active compounds exhibiting properties of the zinc-dependent metaLLproteinases 2nd and 9th type blockers which is known to pLay a key roLe in the pathogenesis of the myocardium earLy post-infarction remodeLing. In studying the effect of newLy synthesized compounds on metaLLoproteinase-9 LeveLs in bLood of rats with acute myocardiaL infarction were seLected compound Leader: 1-({4-[(4-chLorobenzoyL)amino]phenyL}suLfonyL-L-proLine, which effectiveLy bLocked the increase of this enzyme Level. Using echocardiography it was demonstrated that the seLected compound-Leader prevents the myocardiaL remodeLing deveLopment in the acute phase of experimentaL myocardiaL infarction, at Least not inferior to the reference inhibitor of metaLLoproteinases - doxycycLine.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>металлопротеиназы 2-го и 9-го типа</kwd><kwd>постинфарктное ремоделирование миокарда</kwd><kwd>производные бензоила-мино(фенилсульфонил)-замещённых циклических аминокислот</kwd><kwd>metaLLproteinases 2nd- and 9th-type</kwd><kwd>post-infarction myocardiaL remodeLing</kwd><kwd>derivatives of the benzoyLamino (phenyLsuLfonyL) amino-substituted cycLic aminoacids</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">Гасанов А.Г., Бершова Т.В. Роль изменений внеклеточного матрикса при возникновении сердечно-сосудистых заболеваний. 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