1. 2023
  2. Synthesis of N-heterocyclic amides based on (+)-camphoric acid and study of their antiviral activity and pharmacokinetics

    Yarovaya, O. I., Baranova, D. V., Sokolova, A. S., Nemolochnova, A. G., Sal'nikova, O. P., Fat'anova, A. V., Rogachev, A. D., Volobueva, A. S., Zarubaev, V. V., Pokrovsky, A. G. & Salakhutdinov, N. F., Mar 2023, In: Russian Chemical Bulletin. 72, 3, p. 807-818 12 p.

    Research output: Contribution to journalArticlepeer-review

  3. Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors

    Mozhaitsev, E. S., Suslov, E. V., Rastrepaeva, D. A., Yarovaya, O. I., Borisevich, S. S., Khamitov, E. M., Kolybalov, D. S., Arkhipov, S. G., Bormotov, N. I., Shishkina, L. N., Serova, O. A., Brunilin, R. V., Vernigora, A. A., Nawrozkij, M. B., Agafonov, A. P., Maksyutov, R. A., Volcho, K. P. & Salakhutdinov, N. F., 1 Jan 2023, In: Viruses. 15, 1, 29.

    Research output: Contribution to journalArticlepeer-review

  4. Synthesis of conjugates of (aR,7S)-colchicine with monoterpenoids and investigation of their biological activity

    Shchegravina, E. S., Usova, S. D., Baev, D. S., Mozhaitsev, E. S., Shcherbakov, D. N., Belenkaya, S. V., Volosnikova, E. A., Chirkova, V. Y., Sharlaeva, E. A., Svirshchevskaya, E. V., Fonareva, I. P., Sitdikova, A. R., Salakhutdinov, N. F., Yarovaya, O. I. & Fedorov, A. Y., 1 Jan 2023, In: Russian Chemical Bulletin. 72, 1, p. 248-262 15 p.

    Research output: Contribution to journalArticlepeer-review

  5. Synthesis of non-symmetric N-benzylbispidinol amides and study of their inhibitory activity against the main protease of the SARS-CoV-2 virus

    Dalinger, A. I., Baev, D. S., Yarovaya, O. I., Chirkova, V. Y., Sharlaeva, E. A., Belenkaya, S. V., Shcherbakov, D. N., Salakhutdinov, N. F. & Vatsadze, S. Z., 1 Jan 2023, In: Russian Chemical Bulletin. 72, 1, p. 239-247 9 p.

    Research output: Contribution to journalArticlepeer-review

  6. Corrigendum: The main protease 3CLpro of the SARS-CoV-2 virus: how to turn an enemy into a helper

    Belenkaya, S. V., Merkuleva, I. A., Yarovaya, O. I., Chirkova, V. Y., Sharlaeva, E. A., Shanshin, D. V., Volosnikova, E. A., Vatsadze, S. Z., Khvostov, M. V., Salakhutdinov, N. F. & Shcherbakov, D., 2023, In: Frontiers in Bioengineering and Biotechnology. 11, 1294266.

    Research output: Contribution to journalArticlepeer-review

  7. The main protease 3CLpro of the SARS-CoV-2 virus: how to turn an enemy into a helper

    Belenkaya, S. V., Merkuleva, I. A., Yarovaya, O. I., Chirkova, V. Y., Sharlaeva, E. A., Shanshin, D. V., Volosnikova, E. A., Vatsadze, S. Z., Khvostov, M. V., Salakhutdinov, N. F. & Shcherbakov, D. N., 2023, In: Frontiers in Bioengineering and Biotechnology. 11, 1187761.

    Research output: Contribution to journalArticlepeer-review

  8. 2022
  9. Nitrogen-Containing Heterocyclic Compounds Obtained from Monoterpenes or Their Derivatives: Synthesis and Properties

    Chernyshov, V. V., Popadyuk, I. I., Yarovaya, O. I. & Salakhutdinov, N. F., Oct 2022, In: Topics in current chemistry (Cham). 380, 5, p. 42 1 p., 42.

    Research output: Contribution to journalReview articlepeer-review

  10. 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 journalArticlepeer-review

  11. Design, Synthesis, and Biological Evaluation of (+)-Camphor- and (−)-Fenchone-Based Derivatives as Potent Orthopoxvirus Inhibitors

    Sokolova, A. S., Kovaleva, K. S., Kuranov, S. O., Bormotov, N. I., Borisevich, S. S., Zhukovets, A. A., Yarovaya, O. I., Serova, O. A., Nawrozkij, M. B., Vernigora, A. A., Davidenko, A. V., Khamitov, E. M., Peshkov, R. Y., Shishkina, L. N., Maksuytov, R. A. & Salakhutdinov, N. F., 20 Jun 2022, In: ChemMedChem. 17, 12, p. e202100771 26 p., e202100771.

    Research output: Contribution to journalArticlepeer-review

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