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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2026 |
| 1. |
N. E. Astakhova, M. S. Kuzmina, D. A. Vasilenko, D. A. Shashurin, V. Yu. Vasileva, A. V. Sudarikova, N. A. Zefirov, E. B. Averina, V. I. Chubinskiy-Nadezhdin, E. R. Milaeva, O. S. Medvedev, O. N. Zefirova, “Substituted 3-aryl-4-nitroisoxazoles as potential blockers of the transport protein GLUT5: molecular design, synthesis and primary biotesting”, Mendeleev Commun., 36:1 (2026), 12–14  |
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2025 |
| 2. |
N. A. Zefirov, E. V. Nurieva, I. A. Elisseev, Sh. A. Khasanov, M. A. Niukalova, V. V. Zarubaev, O. N. Zefirova, “New adamantane-containing compounds targeting rimantadine-resistant influenza virus A/PR/8/34: molecular design, synthesis and SAR study”, Mendeleev Commun., 35:1 (2025), 50–53   |
1
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2024 |
| 3. |
E. V. Nurieva, O. Yu. Kravtsova, A. V. Sydoriuk, E. V. Britikova, V. V. Britikov, N. A. Zefirov, E. R. Milaeva, O. N. Zefirova, “The homodimer approach to the design of a new long-acting depot prodrug of abiraterone”, Mendeleev Commun., 34:4 (2024), 502–504 |
1
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2023 |
| 4. |
E. V. Nurieva, A. A. Alexeev, N. A. Zefirov, E. R. Milaeva, N. V. Kovaleva, A. N. Proshin, G. F. Makhaeva, O. N. Zefirova, “Annulated bicyclic isothioureas: identification of active and selective butyrylcholinesterase inhibitors”, Mendeleev Commun., 33:1 (2023), 77–79 |
7
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2022 |
| 5. |
A. A. Alexeev, E. V. Nurieva, I. A. Elisseev, E. R. Milaeva, K. A. Lyssenko, O. N. Zefirova, “Bicyclic isothioureas for conjugation with tubulin targeted anticancer agents”, Mendeleev Commun., 32:6 (2022), 766–768 |
| 6. |
N. A. Zefirov, A. Glassl, E. V. Radchenko, A. N. Borovik, V. V. Stanishevskiy, E. R. Milaeva, S. A. Kuznetsov, O. N. Zefirova, “Podophyllotoxin esters with alicyclic residues: an insight into the origin of microtubule-curling effect in cancer cells”, Mendeleev Commun., 32:2 (2022), 173–175 |
10
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2021 |
| 7. |
A. V. Evdokimova, A. A. Alexeev, E. V. Nurieva, E. R. Milaeva, S. A. Kuznetsov, O. N. Zefirova, “N-(4-Methoxyphenyl)-substituted bicyclic isothioureas: effect on morphology of cancer cells”, Mendeleev Commun., 31:3 (2021), 288–290 |
6
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2020 |
| 8. |
E. V. Nurieva, N. A. Zefirov, N. Fritsch, E. R. Milaeva, S. A. Kuznetsov, O. N. Zefirova, “Molecular design and synthesis of new heterobivalent compounds based on chlorambucil and colchicine”, Mendeleev Commun., 30:6 (2020), 706–708 |
5
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| 9. |
N. A. Zefirov, Yu. A. Evteeva, A. I. Krasnoperova, A. V. Mamaeva, E. R. Milaeva, S. A. Kuznetsov, O. N. Zefirova, “Tubulin targeted antimitotic agents based on adamantane lead compound: synthesis, SAR and molecular modeling”, Mendeleev Commun., 30:4 (2020), 421–423 |
13
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| 10. |
E. V. Nurieva, A. A. Alexeev, Yu. K. Grishin, V. A. Tafeenko, O. N. Zefirova, “New compounds with 4-azatricyclo[4.3.1.1<sup>3,8</sup>]undecane framework”, Mendeleev Commun., 30:2 (2020), 145–146 |
4
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| 11. |
N. A. Zefirov, L. Gädert, A. R. Fatkulin, V. M. Shibilev, G. M. Butov, V. M. Mokhov, S. A. Kuznetsov, O. N. Zefirova, “Tubuloclustin analogues with ether moiety: synthesis and evaluation of tubulin clustering and antimitotic activity in cancer cells”, Mendeleev Commun., 30:1 (2020), 106–108 |
10
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| 12. |
N. A. Lozinskaya, N. A. Maximova, D. R. Bazanov, S. E. Sosonyuk, B. Wobith, N. A. Zefirov, E. V. Kharitonashvili, O. N. Zefirova, S. A. Kuznetsov, M. V. Proskurnina, “Synthesis and biotesting of new carrier prodrugs of 2-methoxyestradiol”, Mendeleev Commun., 30:1 (2020), 7–9 |
3
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2019 |
| 13. |
A. A. Alexeev, E. V. Nurieva, T. P. Trofimova, E. A. Chesnakova, Yu. K. Grishin, K. A. Lyssenko, M. V. Filimonova, O. N. Zefirova, “Bicyclic bridged isothioureas: synthesis and evaluation of activity in a model of lipopolysaccharide-induced septic shock”, Mendeleev Commun., 29:1 (2019), 14–16 |
12
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2018 |
| 14. |
N. A. Zefirov, A. Kruth, B. Wobith, E. V. Nurieva, S. Riyaz, Ch. Venkata Ramana Reddy, S. A. Kuznetsov, O. N. Zefirova, “Novel bridged and caged C<sup>4</sup>-podophyllotoxin derivatives as microtubule disruptors: synthesis, cytotoxic evaluation and structure–activity relationship”, Mendeleev Commun., 28:5 (2018), 475–478 |
7
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| 15. |
E. V. Nurieva, T. P. Trofimova, A. A. Alexeev, A. N. Proshin, E. A. Chesnakova, Yu. K. Grishin, K. A. Lyssenko, M. V. Filimonova, S. O. Bachurin, O. N. Zefirova, “Synthesis and antihypotensive properties of 2-amino-2-thiazoline analogues with enhanced lipophilicity”, Mendeleev Commun., 28:4 (2018), 390–392 |
12
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| 16. |
N. A. Zefirov, M. Hoppe, I. V. Kuznetsova, N. A. Chernyshov, Yu. K. Grishin, O. A. Maloshitskaya, S. A. Kuznetsov, O. N. Zefirova, “Homologous series of novel adamantane–colchicine conjugates: synthesis and cytotoxic effect on human cancer cells”, Mendeleev Commun., 28:3 (2018), 308–310 |
10
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2017 |
| 17. |
E. V. Nurieva, N. A. Zefirov, A. V. Mamaeva, Yu. K. Grishin, S. A. Kuznetsov, O. N. Zefirova, “Synthesis of non-steroidal 2-methoxyestradiol mimetics based on the bicyclo[3.3.1]nonane structural motif”, Mendeleev Commun., 27:3 (2017), 240–242 |
6
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| 18. |
D. A. Vasilenko, E. B. Averina, N. A. Zefirov, B. Wobith, Yu. K. Grishin, V. B. Rybakov, O. N. Zefirova, T. S. Kuznetsova, S. A. Kuznetsov, N. S. Zefirov, “Synthesis and antimitotic activity of novel 5-aminoisoxazoles bearing alkoxyaryl moieties”, Mendeleev Commun., 27:3 (2017), 228–230 |
20
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2014 |
| 19. |
D. V. Shishov, E. V. Nurieva, N. S. Zefirov, A. V. Mamaeva, O. N. Zefirova, “Synthesis of 5-hydroxy-4-methoxytricyclo[7.3.1.0<sup>2,7</sup>]trideca-2,4,6-trien- 8-one – precursor of putative bioisosteric colchicine analogues”, Mendeleev Commun., 24:6 (2014), 370–371 |
4
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2013 |
| 20. |
O. N. Zefirova, E. D. Plotnikova, E. V. Nurieva, D. I. Peregud, M. V. Onufriev, N. V. Gulyaeva, “Synthesis of 2-thia-4-azabicyclo[3.3.1]non-3-en-3-amine – bridged nitric oxide synthase inhibitor with enhanced lipophilicity”, Mendeleev Commun., 23:2 (2013), 76–77 |
11
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2012 |
| 21. |
O. N. Zefirova, T. Yu. Baranova, K. A. Lyssenko, N. A. Zefirov, N. V. Zyk, P. M. Vassiliev, D. S. Yakovlev, A. A. Spasov, “Synthesis and biological testing of conformationally restricted serotonin analogues with bridgehead moieties”, Mendeleev Commun., 22:2 (2012), 75–77 |
6
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2011 |
| 22. |
O. N. Zefirova, N. N. Moiseeva, E. V. Nurieva, T. P. Trofimova, A. N. Proshin, Yu. L. Slovokhotov, “Molecular and crystal structures of hetero-analogues of bicyclo[3.3.1]nonane with nitrogen and sulfur atoms”, Mendeleev Commun., 21:5 (2011), 247–249 |
6
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| 23. |
O. N. Zefirova, I. S. Raguzin, V. V. Gogol, E. V. Nurieva, M. S. Belenikin, “Phosphates of bridgehead alcohols as putative inositol monophosphatase inhibitors: molecular design and synthetic approach”, Mendeleev Commun., 21:5 (2011), 242–244 |
7
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2010 |
| 24. |
O. N. Zefirova, E. V. Nurieva, V. I. Chupakhin, I. S. Semenova, D. I. Peregud, M. V. Onufriev, N. V. Gulyaeva, “Design, synthesis and biotest of a bicyclo[3.3.1]nonane analogue of 2-amino-5,6-dihydro-4H-1,3-thiazine”, Mendeleev Commun., 20:6 (2010), 323–325 |
18
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2009 |
| 25. |
T. Yu. Baranova, N. V. Averina, N. V. Zyk, N. S. Zefirov, K. A. Lyssenko, M. Yu. Antipin, O. N. Zefirova, “Synthesis of indole derivatives fused with bicyclo[3.2.1]octane framework”, Mendeleev Commun., 19:1 (2009), 10–11 |
6
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2008 |
| 26. |
O. N. Zefirova, E. V. Nurieva, H. Lemcke, A. A. Ivanov, N. V. Zyk, D. G. Weiss, S. A. Kuznetsov, N. S. Zefirov, “Design, synthesis and bioactivity of simplified taxol analogues on the basis of bicyclo[3.3.1]nonane derivatives”, Mendeleev Commun., 18:4 (2008), 183–185 |
22
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2007 |
| 27. |
O. N. Zefirova, E. V. Nurieva, V. N. Nuriev, K. A. Potekhin, A. V. Maleev, N. V. Zyk, N. S. Zefirov, “Crystal structure of the tritylated product of 3-hydroxymethylbicyclo[3.3.1]nonan-2-on-7-ol ethylene acetal cyclization”, Mendeleev Commun., 17:6 (2007), 332–334 |
1
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2001 |
| 28. |
О. Н. Зефирова, Н. С. Зефиров, “Физиологически активные соединения, взаимодействующие с серотониновыми (5-гидрокситриптаминовыми) рецепторами”, Усп. хим., 70:4 (2001), 382–407 ; O. N. Zefirova, N. S. Zefirov, “Physiologically active compounds interacting with serotonin (5-hydroxytryptamine) receptors”, Russian Chem. Reviews, 70:4 (2001), 333–355 |
6
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1986 |
| 29. |
О. И. Левина, К. А. Потехин, Е. Н. Куркутова, Ю. Т. Стручков, О. Н. Зефирова, В. А. Палюлин, Н. С. Зефиров, “Кристаллическая и молекулярная структура комплекса $1:1$ $3{,}7$-диметил-$1{,}5$-дифенилбиспидона-$9$ с хлоридом меди $(\mathrm{II})$”, Докл. АН СССР, 289:4 (1986), 876–879 |
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