Cytotoxic Copper(II) Complexes Based on 2,2'-Bipyridine/1,10- Phenanthroline and 5-(4-Chlorophenyl)-1H-tetrazole: Synthesis and Structures

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Five coordination compounds [Cu2(Bipy)2L4]·C2H5OH (Iа, Ib), [Cu2(Dmbipy)2L4] (II),
[Cu2(Phen)2L4]·H2O (IIIa), [Cu2(Dmphen)2L4] (IVa), and [Cu2(Phendione’)2L4]·2C2H5OH·2H2O (V) are
synthesized from 5-(4-chlorophenyl)-1H-tetrazole (HL), where Bipy is 2,2'-bipyridine, Dmbipy is 4,4'-
dimethyl-2,2'-bipyridine, Phen is 1,10-phenanthroline, Dmphen is 4,7-dimethyl-1,10-phenanthroline, and
Phendione’ is 6-ethoxy-6-hydroxy-1,10-phenanthrolin-5-one. The crystal structures of the complexes are
determined by X-ray diffraction (XRD) of single crystals (CIF files CCDC nos. 2225368 (Ia), 2225369 (Ib),
2225370 (II), 2225372 (IIIa), 2225373 (IVa), and 2225371 (V)). The compounds are binuclear due to the
bridging function of the tetrazolate anion, and the coordination number of copper is five in all synthesized
complexes. The cytotoxic activity of the complexes against the Hep2 and HepG2 cancer cell lines and noncancerous
human fibroblasts MRC-5 is studied. The complexes exhibit pronounced cytotoxic properties, and
compound V has the maximum selectivity index with respect to the cancer cells.

作者简介

Yu. Golubeva

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia

Email: lisalider@ngs.ru
Россия, Новосибирск

K. Smirnova

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia

Email: lisalider@ngs.ru
Россия, Новосибирск

L. Klyushova

Research Institute of Molecular Biology and Biophysics, Federal Research Center of Fundamental and Translational Medicine,
Novosibirsk, Russia

Email: lisalider@ngs.ru
Россия, Новосибирск

A. Berezin

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia

Email: lisalider@ngs.ru
Россия, Новосибирск

E. Lider

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia

编辑信件的主要联系方式.
Email: lisalider@ngs.ru
Россия, Новосибирск

参考

  1. Rosenberg B., VanCamp L., Trosko J.E. et al. // Nature. 1969. V. 222. № 5191. P. 385.
  2. Ferraro M.G., Piccolo M., Misso G. et al. // Pharmaceutics. 2022. V. 14. № 5. P. 954.
  3. González-Ballesteros M.M., Mejía C., Ruiz-Azuara L. // FEBS Open Bio. 2022. V. 12. № 5. P. 880.
  4. McGivern T.J.P., Afsharpour S., Marmion C.J. // Inorg. Chim. Acta. 2018. V. 472. P. 12.
  5. Erxleben A. // Coord. Chem. Rev. 2018. V. 360. P. 92.
  6. Molinaro C., Martoriati A., Pelinski L. et al. // Cancers. 2020. V. 12. № 10. P. 2863.
  7. Kalinowski D.S., Stefani C., Toyokuni S. et al. // Biochim. Biophys. Acta, Mol. Cell Res. 2016. V. 1863. № 4. P. 727.
  8. Jiang Y., Huo Z., Qi X. et al. // Nanomedicine. 2022. V. 17. № 5. P. 303.
  9. Pinheiro A.C., Busatto F.F., Schaefer B.T. et al. // J. Inorg. Biochem. 2022. V. 237. P. 112013.
  10. Dinev D., Popova K.B., Zhivkova T. et al. // Appl. Organomet. Chem. 2022. V. 36. № 10. P. e6862.
  11. Cao H.Z., Yang W.T., Zheng P.S. // BMC Cancer. 2022. V. 22. № 1. P. 1.
  12. Babahan-Bircan I., Emirdağ S., Özmen A. et al. // Appl. Organomet. Chem. 2022. V. 36. № 9. P. e6784.
  13. Afroz L., Khan M.H.M., Vagdevi H.M. et al. // Emergent Mater. 2021. V. 5. № 4. P. 1133.
  14. Khursheed S., Siddique H.R., Tabassum S. et al. // Dalton Trans. 2022. V. 51. № 31. P. 11713.
  15. Santini C., Pellei M., Gandin V. et al. // Chem. Rev. 2013. V. 114. № 1. P. 815.
  16. Krasnovskaya O., Naumov A., Guk D. et al. // Int. J. Mol. Sci. 2020. V. 21. P. 3965.
  17. Vitomirov T., Dimiza F., Matić I.Z. et al. // J. Inorg. Biochem. 2022. V. 235. P. 111942.
  18. Figueroa-Depaz Y., Pérez-Villanueva J., Soria-Arteche O. et al. // Molecules. 2022. V. 27. № 11. P. 3504.
  19. Karpagam S., Mamindla A., Kumar Sali V. et al. // Inorg. Chim. Acta. 2022. V. 531. P. 120729.
  20. Zehra S., Cirilli I., Silvestri S. et al. // Metallomics. 2021. V. 13. № 11. P. mfab064.
  21. Zehra S., Gómez-Ruiz S., Siddique H.R. et al. // Dalton Trans. 2020. V. 49. № 46. P. 16830.
  22. Paixão D.A., de Oliveira B.C.A., Almeida J.C. et al. // Inorg. Chim. Acta. 2020. V. 499. P. 119164.
  23. Karpagam S., Kartikeyan R., Paravai N.P. et al. // J. Coord. Chem. 2019. V. 72. № 18. P. 3102.
  24. Alvarez N., Mendes L.F.S., Kramer M.G. et al. // Inorg. Chim Acta. 2018. V. 483. P. 61.
  25. Figueroa-DePaz Y., Resendiz-Acevedo K., Dávila-Manzanilla S.G. et al. // J. Inorg. Biochem. 2022. V. 231. P. 111772.
  26. Kumari J., Mobin S.M., Mukhopadhyay S. et al. // Inorg. Chem. Commun. 2019. V. 105. P. 217.
  27. Stoll S., Schweiger A. // J. Magn. Reson. 2006. V. 178. № 1. P. 42.
  28. Bruker Apex3 Software Suite: Apex3, SADABS-2016/2 and SAINT. Version 2018.7-2. Madison (WI, USA): Bruker AXS Inc., 2017.
  29. CrysAlisPro 1.171.38.46. The Woodlands (TX, USA), Rigaku Oxford Diffraction, 2015.
  30. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. № 1. P. 3.
  31. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. № 1. P. 3.
  32. Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Crystallogr. 2009. V. 42. № 2. P. 339.
  33. Eremina J.A., Lider E.V., Samsonenko D.G. et al. // Inorg. Chim. Acta. 2019. V. 487. P. 138.
  34. Smirnova K.S., Golubeva Y.A., Lider E.V. // Crystallogr. Rep. 2022. V. 67. № 4. P. 575.
  35. Eremina J.A., Ermakova E.A., Smirnova K.S. et al. // Polyhedron. 2021. V. 206. P. 115352

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版权所有 © Ю.А. Голубева, К.С. Смирнова, Л.С. Клюшова, А.С. Березин, Е.В. Лидер, 2023