Copper(II) сomplexes with 2-hydrохy-5-ethylphenylphosphosphonic acid: synthesis, structure, cytotoxicity, and accumulation in HeLa cells

Capa

Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Acesso é pago ou somente para assinantes

Resumo

In order to study the physicochemical and biological properties of the coordination compounds of bioactive metal ions with 2-hydroxyphenylphosphonic acid derivatives, the reaction of 2-hydroxy-5-ethylphenylphosphonic acid (Н3L1) with copper(II) perchlorate, sulfate, nitrate, and acetate in water was studied for the first time. It has been established that, regardless of the ratio of reagents, in the case of copper(II) perchlorate, sulfate, and nitrate, a complex of the composition [Cu(H2L1)2(Н2О)2] is formed in high yield, while in the case of using copper(II) acetate a complex [Cu(HL1)(H2O)2] is formed, the composition of which is established on the basis of a combination of elemental analysis data, IR and electronic spectra. Quantum-chemical calculations of the structure of [Cu(H2L1)2(H2O)2] and [Cu(HL1)(H2O)2] complexes were performed for the first time by the density functional theory (DFT) method. The cytotoxic properties of H3L1 acid and copper complexes [Cu(HL1)(H2O)2] and [Cu(H2L1)2(H2O)2] with respect to HeLa tumor cells of human cervical adenocarcinoma were studied. The accumulation of the resulting copper(II) complexes in HeLa cells was proved by laser confocal microscopy.

Sobre autores

Yu. Rogacheva

Institute of Physiologically Active Substances of the Federal Research Center for Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

M. Lapshina

Institute of Physiologically Active Substances of the Federal Research Center for Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

V. Baulin

Institute of Physiologically Active Substances of the Federal Research Center for Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences

Email: mager1988@gmail.com

Bibliografia

  1. Zhang C., Lippard S. // Curr. Opin. Chem. Biol. 2003. Vol. 7. P. 481. doi: 10.1016/s1367-5931(03)00081-4
  2. Hambley T. // Science. 2007. Vol. 318. P. 1392. doi: 10.1126/science.1150504
  3. Barry N., Sadler P. // ACS Nano. 2013. Vol. 7. P. 5654. doi: 10.1021/nn403220e.
  4. Patra M., Gasser G. // Chem. Bioсhem. 2012. Vol. 13. P. 1232. doi: 10.1002/cbic.201200159
  5. Yu G., Jiang M., Huang F., Chen X. // Curr. Opin. Chem. Biol. 2021. Vol. 61. P. 19. doi: 10.1016/j.cbpa.2020.08.0076
  6. Pöthig A., Casini A. // Theranostics. 2019. Vol. 9. P. 3150. doi: 10.7150/thno.31828-6
  7. Mehrotra R., Bohra R., Gaur D. Metal β-diketonates and allied derivatives. London; New York: Academic Press, 1978. P. 382.
  8. Solomon E., Heppner D., Johnston E., Ginsbach J., Cirera J., Qayyum M., Kieber-Emmons M., Kjaergaard C., Hadt R., Tian L. // Chem. Rev. 2014. Vol. 114. P. 3659. doi: 10.1021/cr400327t
  9. Hussain A., AlAjmi M., Rehman M., Rehman M., Amir S., Husain F., Alsalme A., Siddiqui M., AlKhedhairy A., Khan R. // Sci. Rep. 2019. Vol. 9. P. 5237. doi: 10.1038/s41598-019-41063-x
  10. Iakovidis I., Delimaris I., Piperakis S. // Mol. Biol. Int. 2011. P. 594529. doi: 10.4061/2011/594529
  11. Tabti1 R., Tounsi N., Gaiddon C., Bentouhami E., Désaubry L. // Med. Chem. 2017. Vol. 75. P. 875. doi: 10.4172/2161-0444.1000445
  12. Dalecki A., Crawford C., Wolschendorf F. // Rev. Adv. Microb. Physiol. 2017. Vol. 70. P. 193. doi: 10.1016/bs.ampbs.2017.01.007
  13. Arredondo M., Nunez M. // Mol. Aspects Med. 2005. Vol. 26. N 4-5. P. 313. doi: 10.1016/j.mam.2005.07.010
  14. Uriu-Adams J., Keen C. // Mol. Aspects Med. 2005. Vol. 26. N 4-5. P. 268. doi: 10.1016/j.mam.2005.07.015
  15. Crisponi G., Nurchi V., Fanni D., Gerosa C., Nemolato S., Faa G. // Coord Chem Rev. 2010. Vol. 254 P. 876. doi: 10.1016/j.ccr.2009.12.018
  16. Weder J., Dillon C., Hambley T., Kennedy T., Lay B., Biffin P., Regtop J., Davies H. // Coord Chem Rev. 2002. Vol. 232. P. 95. doi: 10.1016/s0010-545(02)00086-3.
  17. Muñoz C., López M., Olivares M., Pizarro F., Arredondo M., Araya M. // Eur. Cytokine Netw. 2005. Vol. 16. N 4. P. 261.
  18. Ott I, Gust R. // Arch. Pharm. Chem. Life Sci. 2007. Vol. 340. N 3. P. 117. doi: 10.1002/ardp.200600151
  19. González-Vílchez F., Vilaplana R. Metallotherapeutic Drugs and Metal-Based Diagnostic Agents. The Use of Metals in Medicine. New York: John Wiley & Sons, Ltd., 2005. P. 219. doi: 10.1002/0470864052.ch12
  20. Szymański P., Frączek T., Markowicz M., Mikiciuk-Olasik Е. // Biometals. 2012. Vol. 25. P. 1089. doi: 10.1007/s10534-012-9578-y
  21. Орлов А.П., Трофимова Т.П., Орлова М.А. // Изв. АН. Сер. хим. 2022. № 3. С. 415
  22. Orlov A.P., Trofimova T.P., Orlova M.A. // Russ. Chem. Bull. 2022. Vol. 71. N 3. Р. 415. doi: 10.1007/s11172-022-3429-y
  23. Ekinciz D., Senturk M., Kufrevioglu O. // Expert Opin Ther Pat. 2011. Vol. 21. N 12. P. 1831. doi: 10.1517/13543776.2011.636354
  24. Amann R., Peskar B. // Eur. J. Pharmacol. 2002. Vol. 447. P. 1. doi: 10.1016/s0014-2999(02)01828-9
  25. Egorova K., Gordeev E., Ananikov V. // Chem. Rev. 2017. Vol. 117. P. 7132. doi: 10.1021/acs.chemrev.6b00562
  26. Rodriguez-Aller M., Guillarme D., Veuthey J.-L., Gurny R. // J. Drug Deliv. Sci. Technol. 2015. Vol. 30. P. 342. doi: 10.1016/j.jddst.2015.05.009
  27. Баулин В.Е., Калашникова И.П., Вихарев Ю.Б., Вихарева Е.А., Баулин Д.В., Цивадзе А.Ю. // ЖОХ. 2018. № 9. C. 1438
  28. Baulin V.Е., Kalashnikova I.Р., Vikharev Yu.В., Vikharevа Е.А., Baulin D.V., Tsivadze A.Yu. // Russ. J. Gen. Chem. 2018. Vol. 88. N 9. P. 1786. doi: 10.1134/S0044460X18090044
  29. Иванова И.С., Цебрикова Г.С., Лапшина М.А., Рогачева Ю.И., Илюхин А.Б, Соловьев В.П., Пятова Е.Н., Баулин В.Е. // Изв. АН. Сер. хим. 2022. № 11. C. 2365
  30. Ivanova I.S., Tsebrikova G.S., Lapshina M.А., Rogacheva Yu.I., Ilyukhin A.B., Solov'ev V.P., Pyatova E.N., Baulin V.E. // Russ. Chem. Bulletin. Vol. 71. N 11. Р. 2365. doi: 10.1007/s11172-022-3664-2
  31. Иванова И.С., Цебрикова Г.С., Рогачева Ю.И., Илюхин А.Б., Соловьев В.П., Пятова Е.Н., Баулин В.Е. // ЖНХ. 2021. Т. 66. № 12. С. 1723
  32. Ivanova I.S., Tsebrikova G.S., Rogacheva Yu. I., Ilyukhin A.B., Solov'ev V.P., Pyatova E.N., Baulin V.E. // Russ. J. Inorg. Chem. 2021. Vol. 66. N 12. P. 1846. doi: 10.1134/S0036023621120068

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML
Baixar

Declaração de direitos autorais © Russian Academy of Sciences, 2023