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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">From Chemistry Towards Technology Step-By-Step</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">From Chemistry Towards Technology Step-By-Step</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>От химии к технологии шаг за шагом</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="online">2782-1900</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">119502</article-id>
   <article-id pub-id-type="doi">10.52957/2782-1900-2026-7-1-125-135</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>Научные статьи</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>Scientific articles</subject>
    </subj-group>
    <subj-group>
     <subject>Научные статьи</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">Synthesis of 2,4,7,9-tetraphenyl-4,4a,9,9a-tetrahydrothiopyrano[2,3-g]thiochromene-5,10(5aH,10aH)-dione and analysis of its biological activity</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Synthesis of 2,4,7,9-tetraphenyl-4,4a,9,9a-tetrahydrothiopyrano[2,3-g]thiochromene-5,10(5aH,10aH)-dione and analysis of its biological activity</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Немиров</surname>
       <given-names>Даниил Михайлович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Nemirov</surname>
       <given-names>Daniil Mihaylovich</given-names>
      </name>
     </name-alternatives>
     <email>dmnemirov@bk.ru</email>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Овчинников</surname>
       <given-names>Константин Львович</given-names>
      </name>
      <name xml:lang="en">
       <surname>Ovchinnikov</surname>
       <given-names>Konstantin L'vovich</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>кандидат химических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>candidate of chemical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Ярославский государственный технический университет</institution>
    </aff>
    <aff>
     <institution xml:lang="en">Yaroslavl State Technical University</institution>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2026-04-02T18:39:38+03:00">
    <day>02</day>
    <month>04</month>
    <year>2026</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2026-04-02T18:39:38+03:00">
    <day>02</day>
    <month>04</month>
    <year>2026</year>
   </pub-date>
   <volume>7</volume>
   <issue>1</issue>
   <fpage>125</fpage>
   <lpage>135</lpage>
   <history>
    <date date-type="received" iso-8601-date="2026-01-29T00:00:00+03:00">
     <day>29</day>
     <month>01</month>
     <year>2026</year>
    </date>
    <date date-type="accepted" iso-8601-date="2026-03-16T00:00:00+03:00">
     <day>16</day>
     <month>03</month>
     <year>2026</year>
    </date>
   </history>
   <self-uri xlink:href="https://ystu.editorum.ru/en/nauka/article/119502/view">https://ystu.editorum.ru/en/nauka/article/119502/view</self-uri>
   <abstract xml:lang="ru">
    <p>2,4,7,9-Tetraphenyl-4,4a,9,9a-tetrahydro-thiopyrano[2,3-g]thiocromene-5,10(5aH,10aH)-dione has been synthesised. Molecular docking with the GABAB(1) receptor was performed, and its affinity and toxicity were calculated. Computational studies were conducted using the PASS-Online programme to identify substance biological activities.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>2,4,7,9-Tetraphenyl-4,4a,9,9a-tetrahydro-thiopyrano[2,3-g]thiocromene-5,10(5aH,10aH)-dione has been synthesised. Molecular docking with the GABAB(1) receptor was performed, and its affinity and toxicity were calculated. Computational studies were conducted using the PASS-Online programme to identify substance biological activities.</p>
   </trans-abstract>
   <kwd-group xml:lang="en">
    <kwd>2H-thiopyranes</kwd>
    <kwd>molecular docking</kwd>
    <kwd>Diels–Alder heterocyclic reaction</kwd>
    <kwd>GABAB(1) receptor</kwd>
    <kwd>affinity</kwd>
    <kwd>toxicity</kwd>
    <kwd>PASS-Online</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
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 </body>
 <back>
  <ref-list>
   <ref id="B1">
    <label>1.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Mousavi-Ebadia M., Safaei-Ghomi J., Nejad M.J. Synthesis of thiopyran derivativesvia [4+2] cycloaddition reactions. RSC Adv., 2025, 15(14), 11160-11188. DOI: 10.1039/D5RA01222H.</mixed-citation>
     <mixed-citation xml:lang="en">Mousavi-Ebadia M., Safaei-Ghomi J., Nejad M.J. Synthesis of thiopyran derivativesvia [4+2] cycloaddition reactions. RSC Adv., 2025, 15(14), 11160-11188. DOI: 10.1039/D5RA01222H.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B2">
    <label>2.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Storozhok N.M., Drulle A.Ya., Login I.Ya., Dregeris I.Ya., Khrapova N.G., Burlakova E.B. Antioxidant activity of natural and synthetic quinones. Issues of biomedical chemistry, 1995, 41(1), 16-21 (in Russian).</mixed-citation>
     <mixed-citation xml:lang="en">Storozhok N.M., Drulle A.Ya., Login I.Ya., Dregeris I.Ya., Khrapova N.G., Burlakova E.B. Antioxidant activity of natural and synthetic quinones. Issues of biomedical chemistry, 1995, 41(1), 16-21 (in Russian).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B3">
    <label>3.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Fedorov S.N., Bode A.M., Dong Z., Radchenko O.S., Shubina L.K., Stonik V.A. Patent of the Russian Federation No. 2411229, 2011 (in Russian).</mixed-citation>
     <mixed-citation xml:lang="en">Fedorov S.N., Bode A.M., Dong Z., Radchenko O.S., Shubina L.K., Stonik V.A. Patent of the Russian Federation No. 2411229, 2011 (in Russian).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B4">
    <label>4.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ibragimova T.V. Quinones and quinoid compounds. Izv. CHGPU, ser. 2. Natural and Technical Sciences, 2020, 104-107 (in Russian).</mixed-citation>
     <mixed-citation xml:lang="en">Ibragimova T.V. Quinones and quinoid compounds. Izv. CHGPU, ser. 2. Natural and Technical Sciences, 2020, 104-107 (in Russian).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B5">
    <label>5.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Stoikov I.I., Antipin I.S., Burilov V.A., et al. Organic Chemistry in Russian Universities. Achievements of Recent Years. Russ. J. Org. Chem., 2024, 60(8), 1361-1584. DOI: 10.31857/S0514749224020058.</mixed-citation>
     <mixed-citation xml:lang="en">Stoikov I.I., Antipin I.S., Burilov V.A., et al. Organic Chemistry in Russian Universities. Achievements of Recent Years. Russ. J. Org. Chem., 2024, 60(8), 1361-1584. DOI: 10.31857/S0514749224020058.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B6">
    <label>6.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Karpov I.D., Ovchinnikov K.L., Kolobov A.V. Single-reactor synthesis of 2H-thiopyranes from β aminoenones. Izv. AN, ser. chem., 2023, 72(5), 1279-1282 (in Russian).</mixed-citation>
     <mixed-citation xml:lang="en">Karpov I.D., Ovchinnikov K.L., Kolobov A.V. Single-reactor synthesis of 2H-thiopyranes from β aminoenones. Izv. AN, ser. chem., 2023, 72(5), 1279-1282 (in Russian).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B7">
    <label>7.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Merkulova E.A., Kolobov A.V., Ovchinnikov K.L. A convenient synthesis of 3,4-dihydro-2H-thiopyran-2,3-dicarboxylicacid derivatives. Rus. Chem. Bull., 2019, 68(3), 606-609. DOI: 10.1007/s11172-019-2462-y.</mixed-citation>
     <mixed-citation xml:lang="en">Merkulova E.A., Kolobov A.V., Ovchinnikov K.L. A convenient synthesis of 3,4-dihydro-2H-thiopyran-2,3-dicarboxylicacid derivatives. Rus. Chem. Bull., 2019, 68(3), 606-609. DOI: 10.1007/s11172-019-2462-y.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B8">
    <label>8.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Karakasa T., Motoki S. Chemistry of α,β-Unsaturated Thione Dimers. 2. Reactions of Thiochalcones and 2 Arylidene-1-thiotetralones with Some Olefins and the Parent Ketones of the Thiones. J. Org. Chem., 1979, 44(23), 4151-4155. DOI: 10.1021/jo01337a029.</mixed-citation>
     <mixed-citation xml:lang="en">Karakasa T., Motoki S. Chemistry of α,β-Unsaturated Thione Dimers. 2. Reactions of Thiochalcones and 2 Arylidene-1-thiotetralones with Some Olefins and the Parent Ketones of the Thiones. J. Org. Chem., 1979, 44(23), 4151-4155. DOI: 10.1021/jo01337a029.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B9">
    <label>9.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Mloston G., Urbaniak K., Urbaniak P., Marko A., Linden A., Heimgartner H. First thia-Diels–Alder reactions of thiochalcones with 1,4-quinones. Beilstein J. Org. Chem., 2018, 14(1), 1834-1839. DOI: 10.3762/bjoc.14.156.</mixed-citation>
     <mixed-citation xml:lang="en">Mloston G., Urbaniak K., Urbaniak P., Marko A., Linden A., Heimgartner H. First thia-Diels–Alder reactions of thiochalcones with 1,4-quinones. Beilstein J. Org. Chem., 2018, 14(1), 1834-1839. DOI: 10.3762/bjoc.14.156.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B10">
    <label>10.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Neese F. The ORCA program system. WIRES Comput. Molec. Sci., 2012, 2(1), 73-78. DOI: 10.1002/wcms.81.</mixed-citation>
     <mixed-citation xml:lang="en">Neese F. The ORCA program system. WIRES Comput. Molec. Sci., 2012, 2(1), 73-78. DOI: 10.1002/wcms.81.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B11">
    <label>11.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Neese F., Wennmohs F., Becker U., Riplinger C. The ORCA quantum chemistry program package. J. Chem. Phys., 2020, 152, 224108. DOI: 10.1063/5.0004608.</mixed-citation>
     <mixed-citation xml:lang="en">Neese F., Wennmohs F., Becker U., Riplinger C. The ORCA quantum chemistry program package. J. Chem. Phys., 2020, 152, 224108. DOI: 10.1063/5.0004608.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B12">
    <label>12.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Neese F. Software update: The ORCA program system – Version 6.0. WIRES Comput. Molec. Sci., 2025, 15(2). e70019. DOI: 10.1002/wcms.70019.</mixed-citation>
     <mixed-citation xml:lang="en">Neese F. Software update: The ORCA program system – Version 6.0. WIRES Comput. Molec. Sci., 2025, 15(2). e70019. DOI: 10.1002/wcms.70019.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B13">
    <label>13.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Perdew J.P. Burke K., Ernzerhof M. Generalized Gradient Approximation Made Simple. Phys. Rev. Lett., 1996, 77(18), 3865-3868. DOI: 10.1103/PhysRevLett.77.3865.</mixed-citation>
     <mixed-citation xml:lang="en">Perdew J.P. Burke K., Ernzerhof M. Generalized Gradient Approximation Made Simple. Phys. Rev. Lett., 1996, 77(18), 3865-3868. DOI: 10.1103/PhysRevLett.77.3865.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B14">
    <label>14.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ernzerhof, M. Scuseria G.E. Assessment of the Perdew-Burke-Ernzerhof exchange-correlation functional. J. Chem. Phys., 1999, 110(11), 5029. DOI: 10.1063/1.478401.</mixed-citation>
     <mixed-citation xml:lang="en">Ernzerhof, M. Scuseria G.E. Assessment of the Perdew-Burke-Ernzerhof exchange-correlation functional. J. Chem. Phys., 1999, 110(11), 5029. DOI: 10.1063/1.478401.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B15">
    <label>15.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Caldeweyher E., Ehlert S., Hansen A., Neugebauer H., Spicher S., Bannwarth C., Grimme S.A. Generally applicable atomic-charge dependent London dispersion correction. J. Chem. Phys., 2019, 150(15), 154122. DOI: 10.1063/1.5090222.</mixed-citation>
     <mixed-citation xml:lang="en">Caldeweyher E., Ehlert S., Hansen A., Neugebauer H., Spicher S., Bannwarth C., Grimme S.A. Generally applicable atomic-charge dependent London dispersion correction. J. Chem. Phys., 2019, 150(15), 154122. DOI: 10.1063/1.5090222.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B16">
    <label>16.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Caldeweyher E., Mewes J.M., Ehlert S., Grimme S. Extension and evaluation of the D4 London-dispersion model for periodic systems. Phys. Chem. Chem. Phys., 2020, 22(16), 8499-8512. DOI: 10.1039/D0CP00502A.</mixed-citation>
     <mixed-citation xml:lang="en">Caldeweyher E., Mewes J.M., Ehlert S., Grimme S. Extension and evaluation of the D4 London-dispersion model for periodic systems. Phys. Chem. Chem. Phys., 2020, 22(16), 8499-8512. DOI: 10.1039/D0CP00502A.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B17">
    <label>17.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Weigend, F., Ahlrichs R. Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy. Phys. Chem. Chem. Phys., 2005, 7(18), 3297-3305. DOI: 10.1039/B508541A.</mixed-citation>
     <mixed-citation xml:lang="en">Weigend, F., Ahlrichs R. Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy. Phys. Chem. Chem. Phys., 2005, 7(18), 3297-3305. DOI: 10.1039/B508541A.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B18">
    <label>18.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Rappoport, D., Furche F. Property-optimized Gaussian basis sets for molecular response calculations. J. Chem. Phys., 2010, 133, 134105. DOI: 10.1063/1.3484283.</mixed-citation>
     <mixed-citation xml:lang="en">Rappoport, D., Furche F. Property-optimized Gaussian basis sets for molecular response calculations. J. Chem. Phys., 2010, 133, 134105. DOI: 10.1063/1.3484283.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B19">
    <label>19.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Rappoport, D. Property-optimized Gaussian basis sets for lanthanides. J. Chem. Phys, 2021, 155(12), 124102. DOI: 10.1063/5.0065611.</mixed-citation>
     <mixed-citation xml:lang="en">Rappoport, D. Property-optimized Gaussian basis sets for lanthanides. J. Chem. Phys, 2021, 155(12), 124102. DOI: 10.1063/5.0065611.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B20">
    <label>20.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Neese, F., Kossmann S. Efficient Structure Optimization with Second-Order Many-Body Perturbation Theory: The RIJCOSX-MP2 Method. J. Chem. Theory Comput., 2010, 6(8), 2325-2338. DOI: 10.1021/ct100199k.</mixed-citation>
     <mixed-citation xml:lang="en">Neese, F., Kossmann S. Efficient Structure Optimization with Second-Order Many-Body Perturbation Theory: The RIJCOSX-MP2 Method. J. Chem. Theory Comput., 2010, 6(8), 2325-2338. DOI: 10.1021/ct100199k.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B21">
    <label>21.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Weigend, F. Accurate Coulomb-Fitting Basis Sets for H to Rn. Phys. Chem. Chem. Phys, 2006, 8(9), 1057-1065. DOI: 10.1039/b515623h.</mixed-citation>
     <mixed-citation xml:lang="en">Weigend, F. Accurate Coulomb-Fitting Basis Sets for H to Rn. Phys. Chem. Chem. Phys, 2006, 8(9), 1057-1065. DOI: 10.1039/b515623h.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B22">
    <label>22.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Goldaeva K.V. Molecular docking in medicine. Literature review. JBG, 2024, 4(26), 1-14. DOI: 10.60797/jbg.2024.26.6 (in Russian).</mixed-citation>
     <mixed-citation xml:lang="en">Goldaeva K.V. Molecular docking in medicine. Literature review. JBG, 2024, 4(26), 1-14. DOI: 10.60797/jbg.2024.26.6 (in Russian).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B23">
    <label>23.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Agu P.C., Afiukwa C.A., Orji O.U. Molecular docking as a tool for the discovery of molecular targets of nutraceuticals in diseases management. Sci. Rep., 2023, 13(1), 13398. DOI: 10.1038/s41598-023-40160-2.</mixed-citation>
     <mixed-citation xml:lang="en">Agu P.C., Afiukwa C.A., Orji O.U. Molecular docking as a tool for the discovery of molecular targets of nutraceuticals in diseases management. Sci. Rep., 2023, 13(1), 13398. DOI: 10.1038/s41598-023-40160-2.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B24">
    <label>24.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Aghajani J., Farnia P. Molecular Dynamic Simulations and Molecular Docking as a Potential Way for Designed New Inhibitor Drug without Resistance. Tanaffos, 2022, 21(1), 1-14.</mixed-citation>
     <mixed-citation xml:lang="en">Aghajani J., Farnia P. Molecular Dynamic Simulations and Molecular Docking as a Potential Way for Designed New Inhibitor Drug without Resistance. Tanaffos, 2022, 21(1), 1-14.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B25">
    <label>25.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Tessaro F., Scapozza L. How ‘Protein-Docking’ Translates into the New Emerging Field of Docking Small Molecules to Nucleic Acids? Molecules, 2020, 25(12), 2749. DOI: 10.3390/molecules25122749.</mixed-citation>
     <mixed-citation xml:lang="en">Tessaro F., Scapozza L. How ‘Protein-Docking’ Translates into the New Emerging Field of Docking Small Molecules to Nucleic Acids? Molecules, 2020, 25(12), 2749. DOI: 10.3390/molecules25122749.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B26">
    <label>26.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Bender B.J., Gahbauer S., Luttens A. A practical guide to large-scale docking. Nat. Protoc., 2021, 16(10), 4799 4832. DOI: 10.1038/s41596-021-00597-z.</mixed-citation>
     <mixed-citation xml:lang="en">Bender B.J., Gahbauer S., Luttens A. A practical guide to large-scale docking. Nat. Protoc., 2021, 16(10), 4799 4832. DOI: 10.1038/s41596-021-00597-z.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B27">
    <label>27.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Meli R., Morris G.M., Biggin P.C. Scoring Functions for Protein-Ligand Binding Affinity Prediction using Structure-Based Deep Learning: A Review. Front. bioinform., 2022, 2, 885983. DOI: 10.3389/fbinf.2022.885983.</mixed-citation>
     <mixed-citation xml:lang="en">Meli R., Morris G.M., Biggin P.C. Scoring Functions for Protein-Ligand Binding Affinity Prediction using Structure-Based Deep Learning: A Review. Front. bioinform., 2022, 2, 885983. DOI: 10.3389/fbinf.2022.885983.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B28">
    <label>28.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ong J., Kerr D.I. Clinical Potential of GABAB Receptor Modulators. CNS Drug Rev., 2005, 11(3), 317-334. DOI: 10.1111/j.1527-3458.2005.tb00049.x.</mixed-citation>
     <mixed-citation xml:lang="en">Ong J., Kerr D.I. Clinical Potential of GABAB Receptor Modulators. CNS Drug Rev., 2005, 11(3), 317-334. DOI: 10.1111/j.1527-3458.2005.tb00049.x.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B29">
    <label>29.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Hvastkovs E.G., Rusling J.F. Modern Approaches to Chemical Toxicity Screening. Curr. Opin. Electrochem., 2017, 3(1), 18-22. DOI: 10.1016/j.coelec.2017.03.013.</mixed-citation>
     <mixed-citation xml:lang="en">Hvastkovs E.G., Rusling J.F. Modern Approaches to Chemical Toxicity Screening. Curr. Opin. Electrochem., 2017, 3(1), 18-22. DOI: 10.1016/j.coelec.2017.03.013.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B30">
    <label>30.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Eberhardt J., Santos-Martins D., Tillack A.F., Forli S. AutoDock Vina 1.2.0: New Docking Methods, Expanded Force Field, and Python Bindings. J. Chem. Inf. Model, 2021, 61(8), 3891-3898. DOI: 10.1021/acs.jcim.1c00203.</mixed-citation>
     <mixed-citation xml:lang="en">Eberhardt J., Santos-Martins D., Tillack A.F., Forli S. AutoDock Vina 1.2.0: New Docking Methods, Expanded Force Field, and Python Bindings. J. Chem. Inf. Model, 2021, 61(8), 3891-3898. DOI: 10.1021/acs.jcim.1c00203.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B31">
    <label>31.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Trott O., Olson A.J. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem., 2010, 31(2), 455-461. DOI: 10.1002/jcc.21334.</mixed-citation>
     <mixed-citation xml:lang="en">Trott O., Olson A.J. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem., 2010, 31(2), 455-461. DOI: 10.1002/jcc.21334.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B32">
    <label>32.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Banerjee P., Kemmler E., Dunkel M., Preissner R. ProTox 3.0: a webserver for the prediction of toxicity of chemicals. NAR, 2024, 52(1), 513–520.DOI: 10.1093/nar/gkae303.</mixed-citation>
     <mixed-citation xml:lang="en">Banerjee P., Kemmler E., Dunkel M., Preissner R. ProTox 3.0: a webserver for the prediction of toxicity of chemicals. NAR, 2024, 52(1), 513–520.DOI: 10.1093/nar/gkae303.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B33">
    <label>33.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Filimonov D.A., Lagunin A.A., Gloriozova T.A., Rudik A.V., Druzhilovskii D.S., Pogodin P.V., Poroikov V.V. Prediction of the biological activity spectra of organic compounds using the PASS online web resource. Chem. Heterocycl. Compd., 2014, 50(3), 444-457. DOI:10.1007/s10593-014-1496-1.</mixed-citation>
     <mixed-citation xml:lang="en">Filimonov D.A., Lagunin A.A., Gloriozova T.A., Rudik A.V., Druzhilovskii D.S., Pogodin P.V., Poroikov V.V. Prediction of the biological activity spectra of organic compounds using the PASS online web resource. Chem. Heterocycl. Compd., 2014, 50(3), 444-457. DOI:10.1007/s10593-014-1496-1.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B34">
    <label>34.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Seok C., Baek M., Steinegger M., Park H., Lee G.R., Won J. Accurate protein structure prediction: what comes next? Bio Design, 2021, 9(3), 47-50. DOI: 10.34184/kssb.2021.9.3.47.</mixed-citation>
     <mixed-citation xml:lang="en">Seok C., Baek M., Steinegger M., Park H., Lee G.R., Won J. Accurate protein structure prediction: what comes next? Bio Design, 2021, 9(3), 47-50. DOI: 10.34184/kssb.2021.9.3.47.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B35">
    <label>35.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Shin W.H., Lee G.R., Heo L., Lee H., Seok C. Prediction of Protein Structure and Interaction by GALAXY protein modeling programs. Bio Design, 2014, 2(1), 1-11.</mixed-citation>
     <mixed-citation xml:lang="en">Shin W.H., Lee G.R., Heo L., Lee H., Seok C. Prediction of Protein Structure and Interaction by GALAXY protein modeling programs. Bio Design, 2014, 2(1), 1-11.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B36">
    <label>36.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ko J., Park H., Heo L., Seok C. Galaxy WEB server for protein structure prediction and refinement. Nucleic Acids Res. 2012, 40(1), 294-297. DOI: 10.1093/nar/gks493.</mixed-citation>
     <mixed-citation xml:lang="en">Ko J., Park H., Heo L., Seok C. Galaxy WEB server for protein structure prediction and refinement. Nucleic Acids Res. 2012, 40(1), 294-297. DOI: 10.1093/nar/gks493.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B37">
    <label>37.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Meng E.C., Polacco B.J., Babbitt P.C. Superfamily active site templates. PROTEINS, 2004, 55(4), 962-976. DOI: 10.1002/prot.20099.</mixed-citation>
     <mixed-citation xml:lang="en">Meng E.C., Polacco B.J., Babbitt P.C. Superfamily active site templates. PROTEINS, 2004, 55(4), 962-976. DOI: 10.1002/prot.20099.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B38">
    <label>38.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Becker G., Berger V., Domschke G. Organicum: Practicum in organ. Chemistry in 2 volumes. Moscow : Mir, 1979, 992 p. (in Russian).</mixed-citation>
     <mixed-citation xml:lang="en">Becker G., Berger V., Domschke G. Organicum: Practicum in organ. Chemistry in 2 volumes. Moscow : Mir, 1979, 992 p. (in Russian).</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B39">
    <label>39.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Cava M.P., Levinson M.I. Thionation reactions of Lawesson’s reagents. Tetrahedron, 1985, 41(22), 5061-5087.</mixed-citation>
     <mixed-citation xml:lang="en">Cava M.P., Levinson M.I. Thionation reactions of Lawesson’s reagents. Tetrahedron, 1985, 41(22), 5061-5087.</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B40">
    <label>40.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Pryanishnikov N.D. Practicum on organic chemistry. Moscow: State Scientific and Technical Publishing House of Chemical Literature, 1956, 244 p. (in Russian).</mixed-citation>
     <mixed-citation xml:lang="en">Pryanishnikov N.D. Practicum on organic chemistry. Moscow: State Scientific and Technical Publishing House of Chemical Literature, 1956, 244 p. (in Russian).</mixed-citation>
    </citation-alternatives>
   </ref>
  </ref-list>
 </back>
</article>
