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  1. 2024

  2. Novel Peptide–Drug Conjugates with Dual Anticancer Activity

    O’Flaherty, S., Luzina, O. A., Dyrkheeva, N. S., Krier, Y., Leprince, J., Zakharenko, A. L., Pokrovsky, M. A., Pokrovsky, A. G., Lavrik, O. I., Salakhutdinov, N. F., Varbanov, M., Devocelle, M. & Volcho, K. P., Nov 2024, In: International Journal of Molecular Sciences. 25, 22, 12411.

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

  3. Aminocarbonylation of 2-(N-substituted) 5-iodobenzoates: synthesis of glyoxylamido-anthranilates, their cytotoxicity and molecular modeling study

    Cheremnykh, K. P., Baev, D. S., Nacharova, E. A., Pokrovskii, M. A., Savelyev, V. A., Meshkova, Y. V., Marenina, M. K., Tolstikova, T. G., Pokrovskii, A. G. & Shults, E. E., Jun 2024, In: Chemical Papers. 78, 9, p. 5639-5656 18 p.

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

  4. 2023

  5. 7-ТРИАЗОЛИЛ-ЗАМЕЩЕННЫЕ ГИДРОКСИСПИРОСТАНЫ, ОБЛАДАЮЩИЕ, ЦИТОТОКСИЧЕСКОЙ АКТИВНОСТЬЮ В ОТНОШЕНИИ ОПУХОЛЕВЫХ КЛЕТОК ЧЕЛОВЕКА

    Миронов, М. Е., Покровский, М. А., Емаминиа, Ф., Покровский, А. Г., Шинкаренко, Е. М. & Шульц, Э. Э., 15 Jun 2023, Роспатент - Федеральная служба по интеллектуальной собственности, Patent No. 2798105, 20 Feb 2023, Priority date 20 Feb 2023, Priority No. 2023103830

    Research output: Patent › Patent for invention

  6. Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents

    Mironov, M. E., Rybalova, T. V., Pokrovskii, M. A., Emaminia, F., Gandalipov, E. R., Pokrovskii, A. G. & Shults, E. E., Feb 2023, In: Steroids. 190, 13 p., 109133.

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

  7. Mannich Reaction of Solasodine with Acetylenes and Formaldehyde. Cytotoxicity of N-Propargyl-Substituted Alkaloid Derivatives

    Finke, A. O., Mironov, M. E., Pokrovskii, M. A. & Shults, E. E., Jan 2023, In: Chemistry of Natural Compounds. 59, 1, p. 87-93 7 p.

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

  8. Синтез и оценка цитотоксичности фуранолабданоидов, содержащих 3-аминопропаноильный заместитель в фурановом цикле

    Харитонов, Ю. В., Петрова, Д. А., Шульц, Э. Э., Покровский, М. А. & Покровский, А. Г., 2023, In: Химия в интересах устойчивого развития. 31, 6, p. 737-745 9 p.

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

  9. 2019

  10. 6-(4′-Aryl-1′,2′,3′-triazolyl)-spirostan-3,5-diols and 6-(4′-Aryl-1′,2′,3′-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity

    Mironov, M. E., Oleshko, O. S., Pokrovskii, M. A., Rybalova, T. V., Pechurov, V. K., Pokrovskii, A. G., Cheresis, S. V., Mishinov, S. V., Stupak, V. V. & Shults, E. E., 1 Nov 2019, In: Steroids. 151, p. 108460 10 p., 108460.

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

  11. Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin

    Lipeeva, A. V., Zakharov, D. O., Gatilov, Y. V., Pokrovskii, M. A., Pokrovskii, A. G. & Shults, E. E., 13 Sept 2019, In: ChemistrySelect. 4, 34, p. 10197-10201 5 p.

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

  12. Design, synthesis, cytotoxicity, and molecular modeling study of 2,4,6-trisubstituted pyrimidines with anthranilate ester moiety

    Cheremnykh, K. P., Savelyev, V. A., Pokrovskii, M. A., Baev, D. S., Tolstikova, T. G., Pokrovskii, A. G. & Shults, E. E., 15 Apr 2019, In: Medicinal Chemistry Research. 28, 4, p. 545-558 14 p.

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

  13. Synthetic Transformations of Higher Terpenoids. 37. Synthesis and Cytotoxicity of 4-(Oxazol-2-Yl)-18-Norisopimaranes

    Gromova, M. A., Kharitonov, Y. U. V., Pokrovskii, M. A., Bagryanskaya, I. Y., Pokrovskii, A. G. & Shul’ts, E. E., 15 Jan 2019, In: Chemistry of Natural Compounds. 55, 1, p. 52-59 8 p.

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

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