Synthesis and antiproliferative activity of 2-aryl-aminopyrimidine amides of benzimidazole-substituted phenylcarboxylic acid – new potential protein kinase inhibitors
- 作者: Koroleva E.V.1, Ermolinskaya A.L.1, Ignatovich Z.V.1, Panibrat O.V.2, Hoang T.3, Huynh T.3, Nguyen T.3
-
隶属关系:
- Institute of Chemistry of New Materials, NAS of Belarus
- Institute of Bioorganic Chemistry, NAS of Belarus
- Institute of Chemical Technology, Vietnam Academy of Science and Technology
- 期: 卷 61, 编号 2 (2025)
- 页面: 159-166
- 栏目: Articles
- URL: https://permmedjournal.ru/0514-7492/article/view/684319
- DOI: https://doi.org/10.31857/S0514749225020053
- EDN: https://elibrary.ru/DGIXKF
- ID: 684319
如何引用文章
详细
The results of a study on the synthesis and antiproliferative activity of new phenylcarboxylic acid amides, the structure of which contains pharmacophoric fragments of nitrogen-containing heterocycles – 2-aminopyrimidine, benzimidazole, pyridine, are presented. The synthesis was carried out by acylation of substituted 2-arylaminopyrimidine phenylenediamines with p-benzimidazole-phenylcarboxylic acid chloride or by aminolysis of p-benzimidazolephenylcarboxylic acid with 2-arylaminopyrimidinephenylenediamines. The potential inhibitory activity of the synthesized amides was assessed by in vitro screening of the compounds for antiproliferative activity in models of stable human tumor cell lines K562, HL-60, RPMI 1788, HeLa.
全文:

作者简介
E. Koroleva
Institute of Chemistry of New Materials, NAS of Belarus
编辑信件的主要联系方式.
Email: evk@ichnm.by
ORCID iD: 0000-0002-0300-8011
白俄罗斯, ul. F. Skoriny, 36, Minsk, 220084
A. Ermolinskaya
Institute of Chemistry of New Materials, NAS of Belarus
Email: evk@ichnm.by
ORCID iD: 0000-0002-7228-1900
白俄罗斯, ul. F. Skoriny, 36, Minsk, 220084
Zh. Ignatovich
Institute of Chemistry of New Materials, NAS of Belarus
Email: evk@ichnm.by
ORCID iD: 0000-0003-0259-4140
白俄罗斯, ul. F. Skoriny, 36, Minsk, 220084
O. Panibrat
Institute of Bioorganic Chemistry, NAS of Belarus
Email: evk@ichnm.by
ORCID iD: 0000-0001-7896-4430
白俄罗斯, ul. Kuprevicha, 5, Minsk, 220084
Thi-Kim-Dung Hoang
Institute of Chemical Technology, Vietnam Academy of Science and Technology
Email: evk@ichnm.by
越南, No.1A, Thanh Loc Street, Thanh Loc Ward, District 12, Ho Chi Minh City, 70000
Thi-Kim-Chi Huynh
Institute of Chemical Technology, Vietnam Academy of Science and Technology
Email: evk@ichnm.by
越南, No.1A, Thanh Loc Street, Thanh Loc Ward, District 12, Ho Chi Minh City, 70000
Thi-Cam-Thu Nguyen
Institute of Chemical Technology, Vietnam Academy of Science and Technology
Email: evk@ichnm.by
越南, No.1A, Thanh Loc Street, Thanh Loc Ward, District 12, Ho Chi Minh City, 70000
参考
- Medina-Franco J.L., Giulianotti M.A., Welmaker G. S. Houghten R.A. Drug Discovery. Today. 2013, 18 (9–10), 495–501. doi: 10.1016/j.drudis.2013.01.008
- Proschak E., Stark H., Merk D. J. Med. Chem. 2019, 62, 420–444. doi: 10.1021/acs.jmedchem. 8b00760
- Morphy R. J. Med. Chem. 2010, 53, 1413–1437. doi: 10.1021/jm901132v
- Rodríguez-Soacha D.A., Scheiner M., Decker M. Eur. J. Med. Chem. 2019, 180, 690–706. doi: 10.1016/j.ejmech.2019.07.040
- Kerru N., Singh P., Koorbanally N., Raj R., Kumar V. Eur. J. Med. Chem. 2017, 142, 179–212. doi: 10.1016/j.ejmech.2017.07.033
- Liu T., Wan Y., Xiao Y., Xia C., Duan G. J. Med. Chem. 2020, 63 (17), 8977–9002. doi: 10.1021/acs.jmedchem.0c00491
- Ma X., Lv X., Zhang J. Eur. J. Med. Chem. 2018, 143, 449–463. doi: 10.1016/j.ejmech.2017.11.049
- Borsari Ch., Trader D.J., Tait A., Costi M.P. J. Med. Chem. 2020, 63 (5), 1908–1928. doi: 10.1021/acs.jmedchem.9b01456
- Королева Е.В., Игнатович Ж.И., Синютич Ю.В., Гусак К.Н. ЖОрХ. 2016, 52, 159–196. [Koroleva E.V., Ignatovich Zh.I., Sinyutich Yu.V., Gusak K.N. Russ. J. Org. Chem. 2016, 52, 139–177.] doi: 10.1134/S1070428016020019
- Ertl P., Altmann E., McKenna J.M. J. Med. Chem. 2020, 63 (15), 8408−8418. doi: 10.1021/acs.jmedchem.0c00754
- Meng L., Shan G., Yong W., Xinying Y., Hao F., Xuben H. J. Med. Chem. 2024, 67 (17), 15098–15117. doi: 10.1021/acs.jmedchem.4c00729
- Гросс Э., Майенхоффер И. Пептиды. Основные методы образования пептидных связей М.: Мир. Москва: 1983. 421 с.
- Chan L.C., Cox B.G. J. Org. Chem. 2007, 72 (23), 8863–8869. doi: 10.1021/jo701558y
- Zhang L., Wang X., Wang J., Grinberg N., Krishnamurthy D., Senanayake C.H. Tetrahedron Lett. 2009, 50, 2964–2966. doi: 10.1016/j.tetlet.2009.03.220
- Huynh T.K.C., Nguyen T., Trand N.H.S., Nguyen T.D., Hoang T.K.D. J. Chem. Sci. 2020, 132, 84–91. doi: 10.1007/s12039-020-01783-4
- Королева Е.В., Игнатович Ж.В., Ермолинская А.Л., Синютич Ю.В., Барановский А.В., Махнач С.А. Изв. НАН Беларуси. сер. хим. наук. 2013, 3, 79–84. [Koroleva E.V., Ignatovich Zh.I., Ermolinskaya A.L. Sinyutich Yu.V., Baranovskii A.V., Makhnach S.A. Izvestiya NAN Belarusi. ser. chem.sci. 2013, 3, 79–84.]
- Al-Nasiry S., Geusens N., Hanssens M., Luyten C., Pijnenborg R. Human. Reproduction. 2007, 22, 1304–1309. doi: 10.1093/humrep/dem011
