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  1. Synthesis and analgesic activity of octahydro-2H-chromenols, derivatives of aliphatic ketones

    Il’ina, I. V., Korchagina, D. V., Morozova, E. A., Tolstikova, T. G., Volcho, K. P. & Salakhutdinov, N. F., 1 May 2019, In: Russian Chemical Bulletin. 68, 5, p. 1061-1066 6 p.

    Research output: Contribution to journal › Article › peer-review

  2. Synthesis and analgesic activity of stereoisomers of 2-(3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols

    Pavlova, A., Mikhalchenko, O., Rogachev, A., Il'ina, I., Korchagina, D., Gatilov, Y., Tolstikova, T., Volcho, K. & Salakhutdinov, N., 28 Nov 2015, In: Medicinal Chemistry Research. 24, 11, p. 3821-3830 10 p.

    Research output: Contribution to journal › Article › peer-review

  3. Synthesis and antiviral activity of camphor-based 1,3-thiazolidin-4-one and thiazole derivatives as Orthopoxvirus-reproduction inhibitors

    Sokolova, A. S., Yarovaya, O. I., Bormotov, N. I., Shishkina, L. N. & Salakhutdinov, N. F., 1 Oct 2018, In: MedChemComm. 9, 10, p. 1746-1753 8 p.

    Research output: Contribution to journal › Article › peer-review

  4. Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles

    Oreshko, V. V., Kovaleva, K. S., Mordvinova, E. D., Yarovaya, O. I., Gatilov, Y. V., Shcherbakov, D. N., Bormotov, N. I., Serova, O. A., Shishkina, L. N. & Salakhutdinov, N. F., Aug 2022, In: Molecules. 27, 15, 4761.

    Research output: Contribution to journal › Article › peer-review

  5. Synthesis and biological activity of heterocyclic borneol derivatives

    Sokolova, A. S., Yarovaya, О. I., Shtro, A. A., Borisova, M. S., Morozova, E. A., Tolstikova, T. G., Zarubaev, V. V. & Salakhutdinov, N. F., 1 Mar 2017, In: Chemistry of Heterocyclic Compounds. 53, 3, p. 371-377 7 p.

    Research output: Contribution to journal › Article › peer-review

  6. Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position

    Popadyuk, I. I., Markov, A. V., Morozova, E. A., Babich, V. O., Salomatina, O. V., Logashenko, E. B., Zenkova, M. A., Tolstikova, T. G. & Salakhutdinov, N. F., Nov 2017, In: Steroids. 127, p. 1-12 12 p.

    Research output: Contribution to journal › Article › peer-review

  7. Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors

    Zakharova, O., Luzina, O., Zakharenko, A., Sokolov, D., Filimonov, A., Dyrkheeva, N., Chepanova, A., Ilina, E., Ilyina, A., Klabenkova, K., Chelobanov, B., Stetsenko, D., Zafar, A., Eurtivong, C., Reynisson, J., Volcho, K., Salakhutdinov, N. & Lavrik, O., 15 Aug 2018, In: Bioorganic and Medicinal Chemistry. 26, 15, p. 4470-4480 11 p.

    Research output: Contribution to journal › Article › peer-review

  8. Synthesis and evaluation of camphor and cytisine-based cyanopyrrolidines as DPP-IV inhibitors for the treatment of type 2 diabetes mellitus

    Kuranov, S. O., Tsypysheva, I. P., Khvostov, M. V., Zainullina, L. F., Borisevich, S. S., Vakhitova, Y. V., Luzina, O. A. & Salakhutdinov, N. F., 15 Aug 2018, In: Bioorganic and Medicinal Chemistry. 26, 15, p. 4402-4409 8 p.

    Research output: Contribution to journal › Article › peer-review

  9. Synthesis and Hypoglycemic Activity of Aryl(Hetaryl)Propenoic Cyanopyrrolidine Amides

    Kuranov, S. O., Blokhin, M. E., Borisov, S. A., Khvostov, M. V., Luzina, O. A. & Salakhutdinov, N. F., 1 Sept 2019, In: Russian Journal of Bioorganic Chemistry. 45, 5, p. 374-380 7 p.

    Research output: Contribution to journal › Article › peer-review

  10. Synthesis and Inhibitory Properties of Imines Containing Monoterpenoid and Adamantane Fragments Against DNA Repair Enzyme Tyrosyl-DNA Phosphodiesterase 1 (Tdp1)

    Zakharenko, A. L., Mozhaitsev, E. S., Suslov, E. V., Korchagina, D. V., Volcho, K. P., Salakhutdinov, N. F. & Lavrik, O. I., 1 Jul 2018, In: Chemistry of Natural Compounds. 54, 4, p. 672-676 5 p.

    Research output: Contribution to journal › Article › peer-review

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