|
|
|
Публикации в базе данных Math-Net.Ru |
Цитирования |
|
2024 |
| 1. |
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
|
|
2023 |
| 2. |
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
|
|
2022 |
| 3. |
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 |
|
2021 |
| 4. |
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
|
|
2020 |
| 5. |
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
|
| 6. |
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
|
|
2019 |
| 7. |
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
|
|
2018 |
| 8. |
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
|
| 9. |
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
|
|
2017 |
| 10. |
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
|
|
2014 |
| 11. |
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
|
|
2013 |
| 12. |
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
|
|
2011 |
| 13. |
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
|
| 14. |
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
|
|
2010 |
| 15. |
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
|
|
2008 |
| 16. |
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
|
|
2007 |
| 17. |
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
|
|
2006 |
| 18. |
A. V. Eremkin, S. N. Molkov, O. V. Ershov, Ya. S. Kayukov, O. E. Nasakin, V. A. Tafeenko, E. V. Nurieva, “Synthesis of 2-halo-6-hydroxy-5,5-dimethyl(ethyl)-5,6-dihydro-1H-pyridine-3,4,4-tricarbonitriles by the reaction of tetracyanoethylene with aldehydes”, Mendeleev Commun., 16:2 (2006), 115–117 |
14
|
|
