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Mendeleev Communications, 2013, Volume 23, Issue 4, Pages 202–203
DOI: https://doi.org/10.1016/j.mencom.2013.07.007
(Mi mendc2661)
 

This article is cited in 19 scientific papers (total in 19 papers)

Communications

Target synthesis of bioactive thioglycolurils, based on QSAR predictions

G. A. Gazievaa, Yu. B. Vikharevb, L. V. Anikinab, T. B. Karpovaa, A. N. Kravchenkoa, E. A. Permyakova, I. Svitankoacd

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b Institute of Technical Chemistry, Ural Branch of the Russian Academy of Sciences, Perm, Russian Federation
c Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
d Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
Abstract: Target synthesis of substituted thioglycolurils possessing sedative activity predicted by preliminary 3D-QSAR simulation of bioactive structures has been carried out.
Document Type: Article
Language: English


Citation: G. A. Gazieva, Yu. B. Vikharev, L. V. Anikina, T. B. Karpova, A. N. Kravchenko, E. A. Permyakov, I. Svitanko, “Target synthesis of bioactive thioglycolurils, based on QSAR predictions”, Mendeleev Commun., 23:4 (2013), 202–203
Linking options:
  • https://www.mathnet.ru/eng/mendc2661
  • https://www.mathnet.ru/eng/mendc/v23/i4/p202
  • This publication is cited in the following 19 articles:
    1. M. P. Egorov, V. P. Ananikov, E. G. Baskir, S. E. Boganov, V. I. Bogdan, A. N. Vereshchagin, V. A. Vil', I. L. Dalinger, A. D. Dilman, O. L. Eliseev, S. G. Zlotin, E. A. Knyazeva, V. M. Kogan, L. O. Kononov, M. M. Krayushkin, V. B. Krylov, L. M. Kustov, V. V. Levin, B. V. Lichitsky, M. G. Medvedev, N. E. Nifantiev, O. A. Rakitin, A. M. Sakharov, I. V. Svitanko, G. A. Smirnov, A. Yu. Stakheev, M. A. Syroeshkin, A. O. Terent'ev, Yu. V. Tomilov, E. V. Tretyakov, I. V. Trushkov, L. L. Fershtat, V. A. Chaliy, V. Z. Shirinian, “Current trends in organic chemistry: contribution of the N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences”, Russ Chem Bull, 73:9 (2024), 2423  crossref
    2. I. V. Svitanko, T. S. Pivina, “Molecular modeling in synthesis: from statistical methods to quantum chemistry and practical applications”, Russ Chem Bull, 73:5 (2024), 1093  crossref
    3. L. V. Saloutina, V. I. Saloutin, O. N. Chupakhin, “Synthesis of fluorine-containing N-,O-,S-heterocycles based on perfluorobiacetyl”, Russ Chem Bull, 72:8 (2023), 1725  crossref
    4. Alexei N. Izmest'ev, Galina A. Gazieva, Lada V. Anikina, Sergey A. Pukhov, Valentina A. Karnoukhova, Natalya G. Kolotyrkina, Angelina N. Kravchenko, “Synthesis and evaluation of the antiproliferative activity of new heterylmethylidene derivatives of imidazothiazolotriazinones”, New J. Chem., 45:27 (2021), 12271  crossref
    5. Sergei A. Serkov, Marina A. Es'kova, Natalya V. Sigay, Natalya N. Kostikova, Tatyana N. Volkhina, Natalya G. Kolotyrkina, Galina A. Gazieva, “Synthesis of 1,3-dialkyl-4-[(arylmethylidene)amino]glycolurils”, Chem Heterocycl Comp, 57:6 (2021), 646  crossref
    6. I. Yu. Titov, V. S. Stroylov, P. V. Rusina, I. Svitanko, “Preliminary modelling as the first stage of targeted organic synthesis”, Russian Chem. Reviews, 90:7 (2021), 831–867  mathnet  mathnet  crossref  isi  scopus
    7. V. A. Ivolgina, L. D. Popov, G. A. Gazieva, A. N. Kravchenko, “Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines”, Russ Chem Bull, 69:11 (2020), 2215  crossref
    8. Vladimir V. Baranov, Anton A. Galochkin, Yulia V. Nelyubina, Angelina N. Kravchenko, Nina N. Makhova, “Synthesis and Structure of 1-Substituted Semithioglycolurils”, Synthesis, 52:17 (2020), 2563  crossref
    9. L. V. Anikina, G. A. Gazieva, A. N. Kravchenko, “Nootropic activity of N-(2-acetylaminoethyl)glycolurils”, Russ Chem Bull, 69:3 (2020), 563  crossref
    10. N. N. Makhova, L. I. Belen'kii, G. A. Gazieva, I. L. Dalinger, L. S. Konstantinova, V. V. Kuznetsov, A. N. Kravchenko, M. M. Krayushkin, O. A. Rakitin, A. M. Starosotnikov, L. L. Fershtat, S. A. Shevelev, V. Z. Shirinian, V. N. Yarovenko, “Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems”, Russian Chem. Reviews, 89:1 (2020), 55–124  mathnet  mathnet  crossref  isi  scopus
    11. L.V. Saloutina, A.Ya. Zapevalov, M.I. Kodess, I.N. Ganebnykh, V.I. Saloutin, O.N. Chupakhin, “Synthesis of trifluoromethyl – containing oxo(thioxo)imidazothiazolones and thioglycolurils based on perfluorobiacetyl”, Journal of Fluorine Chemistry, 212 (2018), 144  crossref
    12. G. A. Gazieva, T. V. Nechaeva, N. N. Kostikova, N. V. Sigay, S. A. Serkov, S. V. Popkov, “Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils”, Russ Chem Bull, 67:6 (2018), 1059  crossref
    13. A. N. Kravchenko, V. V. Baranov, G. A. Gazieva, “Synthesis of glycolurils and their analogues”, Russian Chem. Reviews, 87:1 (2018), 89–108  mathnet  mathnet  crossref  isi  scopus
    14. G. A. Gazieva, T. B. Karpova, T. V. Nechaeva, A. N. Kravchenko, “Ring contraction of 1,2,4-triazine derivatives in the synthesis of imidazoles”, Russ Chem Bull, 65:9 (2016), 2172  crossref
    15. Galina A. Gazieva, Lada V. Anikina, Sergei A. Pukhov, Tatyana B. Karpova, Yulia V. Nelyubina, Angelina N. Kravchenko, “Substituted N-aminothioglycolurils containing thiosemicarbazone moiety and their cytotoxic activity in vitro”, Mol Divers, 20:4 (2016), 837  crossref
    16. Galina A. Gazieva, Tatyana B. Karpova, Leonid D. Popov, Yulia V. Nelyubina, Angelina N. Kravchenko, “Synthesis of New Substituted Thioglycolurils via a Tandem Hydrazone Formation‐ Ring Contraction Reaction”, Journal of Heterocyclic Chem, 52:5 (2015), 1390  crossref
    17. Vladimir V. Baranov, Yulia V. Nelyubina, Angelina N. Kravchenko, Natalya G. Kolotyrkina, Ksenia A. Biriukova, “New access to thioglycolurils by condensation of 4,5-dihydroxyimidazolidin-2-ones(thiones) with HSCN”, Tetrahedron Letters, 56:44 (2015), 6085  crossref
    18. E. I. Prokhorov, A. V. Bekker, A. V. Perevoznikov, M. Kumskov, I. Svitanko, “Combining 3D-QSAR and molecular docking for the virtual screening of PARP inhibitors”, Mendeleev Commun., 25:3 (2015), 214–215  mathnet  crossref
    19. I. S. Ryzhkina, Yu. V. Kiseleva, L. I. Murtazina, O. A. Mishina, A. P. Timosheva, S. Yu. Sergeeva, V. V. Baranov, A. N. Kravchenko, A. I. Konovalov, “Self-organization and chirality in the high dilution solutions of glycoluril enantiomers with (R)- and (S)-methionine moieties”, Mendeleev Commun., 25:1 (2015), 72–74  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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