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  1. 2019

  2. 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

  3. 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

  4. 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

  5. 2022

  6. Conjugates of an antimicrobial peptide and usnic acid derivatives targeting resistant cancer cells

    O’Flaherty, S., Krier, Y., Varbanov, M., Лузина, О. А., Покровский, М. А., Покровский, А. Г., Dyrkheeva, N. S., Zakharenko, A. L., Лаврик, О. И., Волчо, К. П., Салахутдинов, Н. Ф. & Devocelle, M., Aug 2022, In: Journal of peptide science. 28, S3, P324.

    Research output: Contribution to journal › Meeting Abstract › peer-review

  7. 2023

  8. SYNTHESIS AND EVALUATION OF THE CYTOTOXICITY OF FURANOLABDANOIDS CONTAINING A 3-AMINOPROPANOYL SUBSTITUENT IN THE FURAN RING

    YU.V., KHARITONOV., D.A., PETROVA., E.E., SHULTS., M.A., POKROVSKII. & A.G., POKROVSKII., 2023, In: Chemistry for Sustainable Development. 31, 6, p. 715-723 9 p.

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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 2024

  14. 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

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