<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">dan</journal-id><journal-title-group><journal-title xml:lang="ru">Доклады Национальной академии наук Беларуси</journal-title><trans-title-group xml:lang="en"><trans-title>Doklady of the National Academy of Sciences of Belarus</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1561-8323</issn><issn pub-type="epub">2524-2431</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">10.29235/1561-8323-2025-69-5-384-391</article-id><article-id custom-type="elpub" pub-id-type="custom">dan-1272</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>ХИМИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CHEMISTRY</subject></subj-group></article-categories><title-group><article-title>Противовирусная активность производных эпоксиизоиндолов по результатам квантово-химических расчетов</article-title><trans-title-group xml:lang="en"><trans-title>Antiviral activity of epoxyisoindole derivatives on the results of quantum chemical calculations</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>Дикусар</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Dikusar</surname><given-names>E. A.</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>Dikusar Evgenij A. – 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 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 – науч. cотрудник.</p><p>Ул. Сурганова, 13, 220072, Минск</p></bio><bio xml:lang="en"><p>Akishina Ekaterina A. – 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>Колесник</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kolesnik</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Колесник Ирина Андреевна – канд. хим. наук, ст. науч. сотрудник.</p><p>Ул. Сурганова, 13, 220072, Минск</p></bio><bio xml:lang="en"><p>Kolesnik Irina A. – Ph. D. (Chemistry), Senior Researcher.</p><p>13, Surganov Str., 220072, Minsk</p></bio><email xlink:type="simple">irynakolesnik93@gmail.com</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>Маргун</surname><given-names>Е. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Margun</surname><given-names>E. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Маргун Екатерина Николаевна – мл. науч. сотрудник.</p><p>Ул. Сурганова, 13, 220072, Минск</p></bio><bio xml:lang="en"><p>Margun Ekaterina N. – Junior Researcher.</p><p>13, Surganov Str., 220072, Minsk</p></bio><email xlink:type="simple">margynen0555@gmail.com</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>Алексеева</surname><given-names>К. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Alekseeva</surname><given-names>K. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Алексеева Ксения Александровна – аспирант.</p><p>Ул. МиклухоМаклая, 6, 117198, Москва</p></bio><bio xml:lang="en"><p>Alekseeva Kseniia A. – Postgraduate Student.</p><p>6, Miklukho-Maklai Str., 117198, Moscow</p></bio><email xlink:type="simple">ka_alekseeva@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Логвиненко</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Logvinenko</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Логвиненко Никита Александрович – студент.</p><p>ул. Миклухо-Маклая, 6, 117198, Москва</p></bio><bio xml:lang="en"><p>Logvinenko Nikita A. – Student.</p><p>6, Miklukho-Maklai Str., 117198, Moscow</p></bio><email xlink:type="simple">n.a.log291003@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бормотов</surname><given-names>Н. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Bormotov</surname><given-names>N. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бормотов Николай Иванович – вед. науч. сотрудник.</p><p>П. Кольцово, 630559, Новосибирская область</p></bio><bio xml:lang="en"><p>Bormotov Nikolai I. – Leading Researcher.</p><p>Koltsovo, 630559, Novosibirsk Region</p></bio><email xlink:type="simple">bormotov_ni@vector.nsc.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Серова</surname><given-names>О. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Serova</surname><given-names>O. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Серова Ольга Алексеевна – науч. сотрудник.</p><p>П. Кольцово, 630559, Новосибирская область</p></bio><bio xml:lang="en"><p>Serova Olga A. – Researcher.</p><p>Koltsovo, 630559, Novosibirsk Region</p></bio><email xlink:type="simple">serova_oa@vector.nsc.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шишкина</surname><given-names>Л. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Shishkina</surname><given-names>L. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шишкина Лариса Николаевна – д-р биол. наук, вед. науч. сотрудник.</p><p>П. Кольцово, 630559, Новосибирская область</p></bio><bio xml:lang="en"><p>Shishkina Larisa Nikolaevna – D. Sc. (Biology), Leading Researcher.</p><p>Koltsovo, 630559, Novosibirsk Region</p></bio><email xlink:type="simple">shish@vector.nsc.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Яровая</surname><given-names>О. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Yarovaya</surname><given-names>O. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Яровая Ольга Ивановна – д-р хим. наук, вед. науч. сотрудник.</p><p>Пр-т Лаврентьева, 9, 9630090, Новосибирск</p></bio><bio xml:lang="en"><p>Yarovaya Olga I. – D. Sc. (Chemistry), Leading Researcher.</p><p>9, Lavrentiev Ave., 630090, Novosibirsk</p></bio><email xlink:type="simple">ooo@nioch.nsc.ru</email><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Поткин</surname><given-names>В. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Potkin</surname><given-names>V. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Поткин Владимир Иванович – академик, д-р хим. наук, профессор, заведующий лабораторией.</p><p>Ул. Сурганова, 13, 220072, Минск</p></bio><bio xml:lang="en"><p>Potkin Vladimir I. – Academician, D. Sc. (Chemistry), Professor, Head of the Laboratory.</p><p>13, Surganov Str., 220072, Minsk</p></bio><email xlink:type="simple">potkin@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><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Российский университет дружбы народов</institution></aff><aff xml:lang="en"><institution>Peoples’ Friendship University of Russia named after Patrice Lumumba</institution></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Государственный научный центр вирусологии и биотехнологии «Вектор» Федеральной службы по надзору в сфере защиты прав потребителей и благополучия человека</institution></aff><aff xml:lang="en"><institution>State Research Center of Virology and Biotechnology “Vector” of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing</institution></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>Новосибирский институт органической химии имени Н. Н. Ворожцова Сибирского отделения Российской академии наук</institution></aff><aff xml:lang="en"><institution>N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of the Siberian Branch of the Russian Academy of Sciences</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>06</day><month>11</month><year>2025</year></pub-date><volume>69</volume><issue>5</issue><fpage>384</fpage><lpage>391</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Дикусар Е.А., Акишина Е.А., Колесник И.А., Маргун Е.Н., Алексеева К.А., Логвиненко Н.А., Бормотов Н.И., Серова О.А., Шишкина Л.Н., Яровая О.И., Поткин В.И., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Дикусар Е.А., Акишина Е.А., Колесник И.А., Маргун Е.Н., Алексеева К.А., Логвиненко Н.А., Бормотов Н.И., Серова О.А., Шишкина Л.Н., Яровая О.И., Поткин В.И.</copyright-holder><copyright-holder xml:lang="en">Dikusar E.A., Akishina E.A., Kolesnik I.A., Margun E.N., Alekseeva K.A., Logvinenko N.A., Bormotov N.I., Serova O.A., Shishkina L.N., Yarovaya O.I., Potkin V.I.</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://doklady.belnauka.by/jour/article/view/1272">https://doklady.belnauka.by/jour/article/view/1272</self-uri><abstract><p>Изучена противовирусная активность 12 азоти кислородсодержащих гетероциклических соединений в отношении вируса осповакцины в культуре клеток Vero и проведено сопоставление полученных данных с результатами квантово-химических расчетов ab initio методом DFT. Установлено, что показатель индекса селективности зависит от токсичности исследуемых соединений. В частности, соединения, содержащие 2,3-дихлорбензильную группу, оказались более токсичными и неперспективными в качестве противовирусных соединений, кроме того, биологическое тестирование показало, что (Е)-азометины, содержащие фрагмент 1,5-диметил-3-оксо-2-фенил-2,3-дигидро-1H-пиразола, противовирусную активность не проявляли. Наиболее перспективными в отношении вируса осповакцины оказались соединения – производные ванилина и ванилаля. Метод предварительного квантово-химического моделирования может позволить еще на стадии планирования работ по синтезу и биотестированию новых химических соединений произвести выявление неперспективных малоактивных структур.</p></abstract><trans-abstract xml:lang="en"><p>The antiviral activity of 12 nitrogenand oxygen-containing heterocyclic compounds was studied by screening against the vaccinia virus in Vero cell culture and the data obtained were compared with the results of ab initio quantum chemical calculations using the DFT (density functional theory) method. The index of selectivity was found to be contingent upon the toxicity of the compounds under study. Compounds containing a 2,3-dichlorobenzyl group were found to be more toxic and unpromising as antiviral compounds. In addition, biological testing showed that (E)-azomethines containing a fragment of 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole showed no antiviral activity. Compounds derived from vanillin and vanillal have proved to be the most promising in relation to the smallpox vaccine virus. The method of preliminary quantum chemical modeling can make it possible to identify unpromising, low-activity structures even at the planning stage of work on the synthesis and bioscreening of new chemical compounds.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>противовирусная активность</kwd><kwd>азотистые гетероциклы</kwd><kwd>квантово-химические расчеты</kwd><kwd>теория функционала плотности</kwd><kwd>граничные молекулярные орбитали</kwd><kwd>метод Фукуи</kwd><kwd>индекс селективности</kwd></kwd-group><kwd-group xml:lang="en"><kwd>antiviral activity</kwd><kwd>nitrogen heterocycles</kwd><kwd>quantum chemical calculations</kwd><kwd>density functional theory</kwd><kwd>frontier molecular orbitals</kwd><kwd>Fukui method</kwd><kwd>selectivity index</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена при финансовой поддержке Российского научного фонда (проект № 2343-10024) и Белорусского республиканского фонда фундаментальных исследований (проект № Х23РНФ-051). Биологические исследования проведены в рамках Государственного задания ФБУН ГНЦ ВБ «Вектор» Роспотребнадзора (№ ГЗ-40/21) и Государственного задания НИОХ СО РАН (№ 075-00365-25-00)</funding-statement><funding-statement xml:lang="en">This work was supported by the Russian Science Foundation (project no. 23-43-10024) and the Belarusian Republican Foundation for Fundamental Research (project no. Х23РНФ-051). Biological studies were conducted within the framework of the State Assignment of the Federal Budgetary Institution of Science State Research Center of Virology and Biotechnology “Vector” of Rospotrebnadzor (no. ГЗ-40/21) and the State Assignment of the Research Institute of Organic Chemistry SB RAS (no. 075-00365-25-00)</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Синтез формилфенил 1-оксо-1,2,3,6,7,7а-гекасагидро-3а,6-эпоксиизоиндол-7-карбоксилатов и их (E)-1,5-диметил-3-оксо-2-фенил-2,3-дигидро-1H-пиразол-4-илиминометильных производных / Е. А. Дикусар [и др.] // Журнал общей химии. – 2024. – Т. 94, № 7. – С. 786–804. https://doi.org/10.31857/S0044460X24070016</mixed-citation><mixed-citation xml:lang="en">Dikusar E. A., Akishina E. A., Zhukovskaya N. A., Kolesnik I. A., Margun E. N., Kovalskaya S. S., Alekseeva K. A., Logvinenko N. A., Menshikova D. I., Grigorev M. S., Potkin V. I. Synthesis of formylphenyl 1-oxo-1,2,3,6,7,7a-hexahydro-3a,6-epoxyisoindole-7-carboxylates ans their (E)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-yliminome-thyl derivatives. Zhurnal obshchei khimii = Journal of General Chemistry, 2024, vol. 94, no. 7, pp. 786–804 (in Russian). https://doi.org/10.31857/S0044460X24070016</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Руководство по экспериментальному (доклиническому) изучению новых фармакологических веществ / под общ. ред. Р. У. Хабриева. – 2-е изд., перераб. и доп. – М., 2005. – 832 с.</mixed-citation><mixed-citation xml:lang="en">Habriev R. U., ed. Guidelines for Experimental (Preclinical) Studies of New Pharmacological Substances. Moscow, 2005. 832 p. (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">General atomic and molecular electronic-structure system / M. W. Shmidt, K. K. Baldridge, J. A. Boatz [et al.] // Journal of Computational Chemistry. − 1993. − Vol. 14, N 11. − P. 1347–1363. https://doi.org/10.1002/jcc.540141112</mixed-citation><mixed-citation xml:lang="en">Shmidt M. W., Baldridge K. K., Boatz J. A., Elbert S. T., Gordon M. S., Jensen J. H., Koseki S., Matsunaga N., Nguyen K. A., Su S., Windus T. L., Dupuis M., Montgomery J. A. General atomic and molecular electronic structure system. Journal of Computational Chemistry, 1993, vol. 14, no. 11, pp. 1347–1363. https://doi.org/10.1002/jcc.540141112</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Gaussian Basis Sets for Molecular Calculations / ed. by S. Huzinaga. − Amsterdam, 1984. − Vol. 16. − 426 p.</mixed-citation><mixed-citation xml:lang="en">Huzinaga S., ed. Gaussian Basis Sets for Molecular Calculations. Amsterdam, 1984, vol. 16. 426 p.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Putz, M. V. DFT chemical reactivity driven by biological activity: applications for the toxicological fate of chlorinated PAHs / M. V. Putz, A. M. Putz // Applications of density functional theory to biological and bioinorganic chemistry. – Berlin, 2013. – P. 181-231. https://doi.org/10.1007/978-3-642-32750-6_6</mixed-citation><mixed-citation xml:lang="en">Putz M. V., Putz A. M. DFT chemical reactivity driven by biological activity: applications for the toxicological fate of chlorinated PAHs. Applications of Density Functional Theory to Biological and Bioinorganic Chemistry, Berlin, 2013, pp. 181-231. https://doi.org/10.1007/978-3-642-32750-6_6</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил} мочевин / Б. А. Селиванов, А. Я. Тихонов, Е. Ф. Беланов [и др.] // Химико-фармацевтический журнал. – 2017. – Т. 51, № 6. – С. 13–17. https://doi.org/10.30906/0023-1134-2017-51-6-13-17</mixed-citation><mixed-citation xml:lang="en">Selivanov B. A., Tikhonov A. Ya., Belanov E. F., Bormotov N. I., Kabanov A. S., Mazurkov O. Yu., Serova O. A., Shishkina L. N., Agafonov A. P., Sergeev A. N. Synthesis and antiviral activity of 1-aryl-3-{3,5-dioxo-4-azatetracyclo[5.3.2.02,6.08,10]-dodec-11-en-4-yl}ureas. Khimiko-farmatsevticheskii zhurnal = Chemical-Pharmaceutical Journal, 2017, vol. 52, no. 6, pp. 13–17 (in Russian). https://doi.org/10.30906/0023-1134-2017-51-6-13-17</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Smallpox (Variola Virus) Infection: Developing Drugs for Treatment or Prevention: Guidance for Industry / U. S. Department of Health and Human Services. – 2019. – November. – P. 13. URL: https://www.fda.gov/media/132623/download (date of access: 29 January 2025).</mixed-citation><mixed-citation xml:lang="en">U. S. Department of Health and Human Services. Smallpox (Variola Virus) Infection: Developing Drugs for Treatment or Prevention: Guidance for Industry. 2019, November, pp. 13. Available at: https://www.fda.gov/media/132623/download (accessed 29 January 2025).</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Дьюар, M. Теория возмущений молекулярных орбиталей / М. Дьюар. – М., 1977. – 696 с.</mixed-citation><mixed-citation xml:lang="en">Ďjuar M. Molecular Orbital Perturbation Theory. Moscow, 1977. 696 p. (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Изучение противовоспалительной активности серии азотистых гетероциклических соединений и сравнение полученных данных с результатами квантово-химических расчетов / Е. А. Дикусар, Е. А. Акишина, С. Г. Стёпин [и др.] // Доклады Национальной академии наук Беларуси. – 2024. – Т. 68, № 6. – С. 454–459. https://doi.org/10.29235/15618323-2024-68-6-454-459</mixed-citation><mixed-citation xml:lang="en">Dikusar E. A., Akishina E. A., Stepin S. G., Mukusheva G. K., Zhasymbekova A. R., Toigambekova N. N., Seidakhmetova R. B., Potkin V. I. Studying the anti-inflammatory activity of a series of nitrogenous heterocyclic compounds and comparison of the obtained data with the results of quantum chemical calculations. Doklady Natsional’noi akademii nauk Belarusi = Doklady of the National Academy of Sciences of Belarus, 2024, vol. 68, no. 6, pp. 454–459 (in Russian). https://doi.org/10.29235/1561-8323-2024-68-6-454-459</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Анализ зависимости биологической активности от некоторых расчетных физических параметров молекул бензоциклопентахинолинов и бензакридинов / В. С. Волобуев, Е. А. Дикусар, Е. А. Акишина, С. С. Шиканов // Веснік Магілёўскага дзяржаўнага ўніверсітэта імя А. А. Куляшова. Серыя В. Прыродазнаўчыя навукі: матэматыка, фізіка, біялогія. – 2024. – № 2 (64). – С. 74–83.</mixed-citation><mixed-citation xml:lang="en">Volobuev V. S., Dikusar E. A., Akishina E. A., Shikanov S. S. Analysis of the dependence of biological activity on some calculated physical parameters of benzocyclopentaquinoline and benzacridine molecules. Vesnіk Magіleўskaga dzyarzhaўnaga ўnіversіteta іmya A. A. Kulyashova. Seryya V. Pryrodaznaўchyya navukі: matematyka, fіzіka, bіyalogіya [Bulletin of the Mogilev State University named after A. A. Kuleshov. Series V. Natural Sciences: Mathematics, Physics, Biology], 2024, no. 2 (64), pp. 74–83 (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Анальгетическая активность серии азотистых гетероциклических соединений: эксперимент и сравнение полученных данных с результатами квантово-химических расчетов ab initio методом DFT / Е. А. Дикусар, Е. А. Акишина, И. А. Колесник [и др.] // Вестник фармации. – 2024. – № 2 (104). – С. 67–74.</mixed-citation><mixed-citation xml:lang="en">Dikusar E. A., Akishina E. A., Kolesnik I. A., Margun E. N., Stepin S. G., Mukusheva G. K., Zhasymbekova A. R., Toigambekova N. N., Nurmaganbetova M. S., Seidakhmetova R. B., Fedoseeva M. A., Simakova D. N., Potkin V. I. Analgesic activity of a series of nitrogenous heterocyclic compounds: experiment and comparison of the data obtained with the results of quantum chemical calculations ab initio using DFT method. Vestnik farmatsii = Pharmacy Bulletin, 2024, no. 2 (104), pp. 67–74 (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Яровая, О. И. Монои сесквитерпены в качестве стартовой платформы для создания противовирусных средств / О. И. Яровая, Н. Ф. Салахутдинов // Успехи химии. – 2021. – Т. 90, № 4. – С. 488–510.</mixed-citation><mixed-citation xml:lang="en">Yarovaya O. I., Salakhutdinov N. F. Monoand sesquiterpenes as a starting platform for the development of antiviral drugs. Russian Chemical Reviews, 2021, vol. 90, no. 4, pp. 488–510. https://doi.org/10.1070/rcr4969</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings / C. A. Lipinski, F. Lombardo, B. W. Dominy, P. J. Feeney // Advanced Drug Delivery Reviews. – 1997. – Vol. 23, N 1–3. – P. 3–25. https://doi.org/10.1016/s0169-409x(96)00423-1</mixed-citation><mixed-citation xml:lang="en">Lipinski C. A., Lombardo F., Dominy B. W., Feeney P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Advanced Drug Delivery Reviews, 2001, vol. 23, no. 1–3, pp. 3–25. https://doi.org/10.1016/s0169-409x(96)00423-1</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">New data on vanillin-based isothiazolic insecticide synergists / A. V. Kletskov, V. I. Potkin, E. A. Dikusar, R. M. Zolotar // Natural Product Communications. – 2017. – Vol. 12, N 1. – P. 105–106. https://doi.org/10.1177/1934578x1701200130</mixed-citation><mixed-citation xml:lang="en">Kletskov A. V., Potkin V. I., Dikusar E. A., Zolotar R. M. New data on vanillin-based isothiazolic insecticide synergists. Natural Product Communications, 2017, vol. 12, no. 1, pp. 105–106. https://doi.org/10.1177/1934578x1701200130</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>
