Three-Component Synthesis and Antibacterial Activity of 5-Aryl-4-Acyl-3-Hydroxy-1-(4-Methoxyphenyl)-3-Pyrroline-2-Ones
- Authors: Kasimova N.N.1, Maiamsina O.O.1,2, Dubrovina S.S.1, Gein V.L.1
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Affiliations:
- Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
- Perm State Medical University named after Academician E. A. Wagner of the Ministry of Health of the Russian Federation
- Issue: Vol 95, No 5-6 (2025)
- Pages: 191-198
- Section: Articles
- URL: https://ogarev-online.ru/0044-460X/article/view/304464
- DOI: https://doi.org/10.31857/S0044460X25050034
- EDN: https://elibrary.ru/fislvd
- ID: 304464
Cite item
Abstract
A series of new 5-aryl-4-acyl-3-hydroxy-1-(4-methoxyphenyl)-3-pyrrolin-2-ones was synthesized by the reacting of methyl esters of aroylpyruvic acids with a mixture of aromatic aldehyde and p-anisidine. Antibacterial activity of the obtained compounds was studied in vitro against Staphylococcus aureus and Escherichia coli strains.
About the authors
N. N. Kasimova
Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
Email: pufmail135@gmail.com
Perm, 614990 Russia
O. O. Maiamsina
Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation; Perm State Medical University named after Academician E. A. Wagner of the Ministry of Health of the Russian Federation
Email: pufmail135@gmail.com
Perm, 614990 Russia; Perm, 614990 Russia
S. S. Dubrovina
Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
Email: pufmail135@gmail.com
Perm, 614990 Russia
V. L. Gein
Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
Author for correspondence.
Email: pufmail135@gmail.com
Perm, 614990 Russia
References
- Afsah E.M., Abdelmageed S.M. // J. Heterocyclic Chem. 2020. Р. 1. doi: 10.1002/jhet.4098
- Manta S., Kollatos N., Mitsos C., Chatzieffraimidi G.-A., Papanastasiou I., Gallos J.K., Komiotis D. // Mini-Rev. Med. Chem. 2020. Vol. 20. N 10. P. 818. doi: 10.2174/1389557520666200103123114
- Гейн О.Н., Рубцова Д.Д., Гейн В.Л. // Хим.-фарм. ж. 2022. Т. 56. № 12. С. 35. doi: 10.30906/0023-1134-2022-56-12-35-37
- Cusumano A.Q., Pierce J.G. // Bioorg. Med. Chem. Lett. 2018. Vol. 28. N 16. P. 2732. doi: 10.1016/j.bmcl.2018.02.047
- Joksimović N., Petronijević J., Janković N., Baskić D., Popović S., Todorović D., Matic S., Bogdanovic G.A., Vranes M., Tot A., Bugarčić Z. // Bioorg. Chem. 2019. Vol. 88. P. 102954. doi: 10.1016/j.bioorg.2019.102954
- Ahankar H., Ramazani А., Slepokura К., Lis Т., Joo S.W. // Green Chem. 2016. N 18. P. 3582. doi: 10.1039/c6gc00157b
- Машковский М.Д. Лекарственные средства. М.: Новая волна, 2024. 1216 с.
- Paguigan N.D., Yan Y., Karthikeyan M., Chase K., Carter J., Leavitt L.S., Lim A.L., Lin Z., Memon T., Christensen S., Bentzen B.H., Schmitt N., Reilly C.A., Teichert R.W., Raghuraman S., Olivera B.M., Schmidt E.W. // ACS Chem. Biol. 2021. Vol. 16. N 9. P. 1654. doi: 10.1021/acschembio.1c00328
- Duncan L.F., Wang G., Ilyichova O.V., Dhouib R., Totsika M., Scanlon M.J., Heras B., Abbott B.M. // Bioorg. Med. Chem. 2021. Vol. 45. P. 116315. doi: 10.1016/j.bmc.2021.116315
- Brown D.W., Denman C., OʼDonnell H. // J. Chem. Soc. (C). 1971. P. 3195. doi: 10.1039/J39710003195
- Ma K., Wang P., Fu W., Wan X., Zhou L., Chu Y., Ye D. // Bioorg. Med. Chem. Lett. 2011. Vol. 21. N 22. P. 6724. doi: 10.1016/j.bmcl.2011.09.054
- Gein V.L., Chalkov D.V., Romanova A.V., Bobrovskaya O.V., Chashchina S.V., Dmitriev M.V. // Russ. J. Org. Chem. 2025. Vol. 61. N 1. P. 16. doi: 10.1134/S1070428025010026
- Гейн В.Л., Гейн Л.Ф., Безматерных Э.Н., Шуров С.Н. // ЖОХ. 2000. Т. 70. Вып. 10. С. 1692.
- Руководство по проведению доклинических исследований лекарственных средств / Под ред. А.Н. Миронова. М.: Гриф и К, 2012. Ч. 1. 944 с.
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