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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">10.37489/2587-7836-2021-4-18-23</article-id><article-id custom-type="elpub" pub-id-type="custom">phkinetica-294</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>Новый глипролин ГЗК-111 с нейропсихотропной активностью</article-title><trans-title-group xml:lang="en"><trans-title>Novel glyproline GZK-111 with neuropsychotropic activity</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6797-692X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Колясникова</surname><given-names>К. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Koliasnikova</surname><given-names>K. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Колясникова Ксения Николаевна - к. б. н., с. н. с. лаборатории пептидных биорегуляторов отдела химии лекарственных средств</p><p>SPIN-код: 5682-2035</p><p>Москва</p></bio><bio xml:lang="en"><p>Koliasnikova Ksenia N. - PhD in Biology, Senior Researcher at the Laboratory of Peptide Bioregulators of the Department of Drug Chemistry</p><p>SPIN code: 5682-2035</p><p>Moscow</p></bio><email xlink:type="simple">kszolotova@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0371-4370</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Аляева</surname><given-names>А. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Alyaeva</surname><given-names>A. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Аляева Анна Григорьевна - м. н. с. лаборатории пептидных биорегуляторов отдела химии лекарственных средств</p><p>Москва</p></bio><bio xml:lang="en"><p>Alyaeva Anna G. -Junior Researcher at the Laboratory of Peptide Bioregulators of the Department of Drug Chemistry</p><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9228-0596</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кузнецова</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuznetsova</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кузнецова Елена Александровна - к. х. н., с. н. с. лаборатории тонкого органического синтеза отдела химии лекарственных средств</p><p>Москва</p></bio><bio xml:lang="en"><p>Kuznetsova Elena A. - PhD in Chemical, Senior Research at the Laboratory of fine organic synthesis Department of medicinal chemistry</p><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">ФГБНУ «Научно-исследовательский институт фармакологии имени В.В. Закусова»<country>Россия</country></aff><aff xml:lang="en">FSBI “Zakusov Institute of Pharmacology”<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">«Научно-исследовательский институт фармакологии имени В.В. Закусова»<country>Россия</country></aff><aff xml:lang="en">FSBI “Zakusov Institute of Pharmacology”<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>22</day><month>02</month><year>2022</year></pub-date><volume>0</volume><issue>4</issue><fpage>18</fpage><lpage>23</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Колясникова К.Н., Аляева А.Г., Кузнецова Е.А., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Колясникова К.Н., Аляева А.Г., Кузнецова Е.А.</copyright-holder><copyright-holder xml:lang="en">Koliasnikova K.N., Alyaeva A.G., Kuznetsova E.A.</copyright-holder><license 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/294">https://www.pharmacokinetica.ru/jour/article/view/294</self-uri><abstract><p>Статья представляет собой обзор собственных работ, в которой описаны конструирование, синтез и фармакологические свойства линейного замещённого глипролина ГЗК-111, потенциального препарата для комплексного лечения психиатрических патологий, включающих тревожные, депрессивные расстройства и нарушения когнитивных функций. Описывается связь структуры и активности в ряду аналогов этого глипролина. Представлены экспериментальные доказательства способности ГЗК-111 метаболизироваться с образованием цикло-пролилглицина, идентичного эндогенному циклическому дипептиду. Приведены данные о токсикологических и фармакокинетических исследованиях ГЗК-111.</p></abstract><trans-abstract xml:lang="en"><p>Thе article represents a review of our own researches, which describes the design, synthesis and pharmacological properties of linear substituted glyproline GZK-111, a potential drug for the complex treatment of psychiatric pathologies, including anxiety, depressive disorders, and cognitive impairment. The relationship between structure and activity in a series of this glyproline analogs is described. The experimental evidence of the GZK-111 ability to metabolized with the formation of cycloprolylglycine, which is identical to the endogenous cyclic dipeptide, is presented. The data on toxicological and pharmacokinetic studies of GZK-111 are presented.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>этиловый эфир N-фенилацетилглицил-L-пролина</kwd><kwd>ГЗК-111</kwd><kwd>цикло-пролилглицин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>N-phenylacetylglycyl-L-proline ethyl ester</kwd><kwd>GZK-111</kwd><kwd>cyclo-prolyl-glycine</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">Гудашева Т.А., Островская Р.У., Максимова Ф.В. и др. Топологические аналоги пирацетама на основе пролина и их ноотропная активность. Химико-фармацевтический журнал. 1989;23(3):276–281.</mixed-citation><mixed-citation xml:lang="en">Гудашева Т.А., Островская Р.У., Максимова Ф.В. и др. Топологические аналоги пирацетама на основе пролина и их ноотропная активность. 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DOI: 10.47056/0365-9615-2021-172-11-618-621.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
