- PII
- 10.31857/S0044457X24050113-1
- DOI
- 10.31857/S0044457X24050113
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 69 / Issue number 5
- Pages
- 736-742
- Abstract
- This article proposes carbocyclic derivatives of N-acylated esters of L-amino acids with aromatic carboxylic acids as antiviral low-molecular agents. To increase the water solubility of inhibitors that are insoluble in aqueous solutions, the target compounds were used in the form of zinc(II) complexes. It has been shown that hydrophobic organic compounds in the form of zinc(II)-coordinated ligands are capable of suppressing the replication of an influenza A virus strain resistant to adamantane-type drugs. Zinc(II) chloride at the concentration used does not have antiviral or toxic effects in experiments in vitro.
- Keywords
- грипп А противовирусная активность растворимость в воде цинк L-аминокислоты ароматические карбоновые кислоты
- Date of publication
- 17.09.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 13
References
- 1. Sarkar A., Mandal K. // Angew. Chem. Int. Ed. Engl. 2021. V. 60. P. 23492. https://doi.org/10.1002/anie.202107481
- 2. Davies W.L., Grunnert R.R., Haff R.F. et al. // Science. 1964. V. 44. P. 862.
- 3. Togo Y., Hornick R.B., Dawkins A.T. // J. Am. Med. Assoc. 1968. V. 203. P. 1089.
- 4. Wendel H.A., Snyder M.T., Pell S. // Clin. Pharmacol. Ther. 1966. V. 7. P. 38.
- 5. Okada A., Miura T., Takeuchi H. // Biochemistry. 2001. V. 40. P. 6053.
- 6. Avdeeva V.V., Garaev T.M., Malinina E.A. et al. // Russ. J. Inorg. Chem. 2022. V. 67. P. 28. https://doi.org/10.1134/S0036023622010028
- 7. Shibnev V.A., Deryabin P.G., Garaev T.M. et al. // Russ. J. Bioorg. Chem. 2017. V. 43. P. 517.
- 8. Garaev T.M., Odnovorov A.I., Grebennikova T.V. et al. // Adv. Pharm. Bull. 2021. V. 11. P. 700.
- 9. Shibnev V.A., Garaev T.M., Finogenova M.P. et al. // Pharm. Chem. J. 2012. V. 46. P. 36.
- 10. Шибнев В.А., Гараев Т.М., Финогенова М.П. и др. Пат. RU 2461544 С1. 2012.
- 11. Климочкин Ю.Н., Леонова М.В., Ширяев А.К. Пат. RU 2553991 С1. 2008.
- 12. Шибнев В.А., Дерябин П.Г., Бурцева Е.И. Пат. RU 2572102 С1. 2014.
- 13. Caetano-Silva M.E., Cilla A., Bertoldo-Pacheco M.T. et al. // J. Food Comp. Anal. 2018. V. 68. P. 95. https://doi.org/10.1016/j.jfca.2017.03.010
- 14. Lebedeva N.S., Mal’kova E.A., Pavlycheva N.A. et al. // Russ. J. Coord. Chem. 2004. V. 30. P. 864. https://doi.org/10.1007/s11173-005-0006-5
- 15. Zhdanova K.A., Savel’eva I.O., Usanev A.Yu. et al. // Russ. J. Inorg. Chem. 2022. V. 67. P. 1756. https://doi.org/10.1134/S0036023622601209
- 16. Dojer B., Golobič A., Babič N. et al. // J. Mol. Struct. 2022. V. 1265. P. 133393. https://doi.org/10.1016/j.molstruc.2022.133393
- 17. Chuprin A.S., Dudkin S.V., Vologzhanina A.V. et al. // Russ. J. Inorg. Chem. 2023. V. 68. P. 713. https://doi.org/10.1134/S003602362360065X
- 18. Jacob W., Mukherjee R. // Inorg. Chim. Acta. 2006. V. 359. P. 4565. https://doi.org/10.1016/j.ica.2006.07.003
- 19. Leite S.M.G., Lima L.M.P., Gama S. et al. // Inorg. Chem. 2016. V. 55. P. 11801. https://doi.org/10.1021/acs.inorgchem.6b01884
- 20. Wei Liao, Ziwei Zhu, Chenglian Feng et al. // J. Environ. Sci. 2023. V. 127. P. 495. https://doi.org/10.1016/j.jes.2022.06.002
- 21. Gur’eva Y.A., Zalevskaya O.A., Kuchin A.V. // Russ. J. Coord. Chem. 2023. V. 49. P. 631. https://doi.org/10.1134/S1070328423700665
- 22. Uvarova M.A., Novikova M.V., Eliseenkova V.A. et al. // Russ. J. Coord. Chem. 2023. V. 49. P. 680. https://doi.org/10.1134/S1070328423600419
- 23. Betancourth J.G., Sánchez-Rodríguez N.E., Giraldo-Dávila D. et al. // Russ. J. Inorg. Chem. 2022. V. 67. P. 2200. https://doi.org/10.1134/S0036023622600782
- 24. Ivanova I.S., Tsebrikova G.S., Ilyukhin A.B. et al. // Russ. J. Inorg. Chem. 2023. https://doi.org/10.1134/S0036023623601393
- 25. Ermakova E.A., Golubeva Y.A., Smirnova K.S. et al. // Russ. J. Coord. Chem. 2023. V. 49. P. 593. https://doi.org/10.1134/S1070328423600158
- 26. Garaev T.M., Yudin I.I., Breslav N.V. et al. // Tetrahedron. 2023. V. 151. № 133785.
- 27. Garaev T., Breslav N., Grebennikova T. et al. // Proc. 9th Int. Electron. Conf. Med. Chem., 1–30 November 2023, MDPI: Basel, Switzerland. https://doi.org/10.3390/ECMC2023–15805
- 28. Garaev T.M., Yudin I.I., Breslav N.V. et al. // Curr. Pharm. Res. 2023 (in press).
- 29. Shibnev V.A., Garaev T.M., Finogenova M.P. et al. // Pharm. Chem. J. 2012. V. 46. P. 1.
- 30. Бурцева Е.И., Шевченко Е.С., Ленева И.А. и др. // Вопр. вирусологии. 2007. № 2. С. 24.
- 31. Лeнeвa И.A., Фaдeeвa Н.И., Фeдякинa И.T. и др. // Хим.-фарм. журн. 1994. № 9. C. 4.
- 32. Шибнев В.А., Дерябин П.Г., Бурцева Е.И. Пат. RU 2624906 С1. 2015.