Synthesis, Structure, and Study of the Cytotoxic Activity of Zinc(II) Complex with 5-Benzyltetrazole and 1,10-Phenanthroline

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Abstract

The complex [Zn(Phen)(H2O)L2] (I), where HL is 5-benzyltetrazole, Phen is 1,10-phenanthroline,
was synthesized. The compound was characterized by standard physicochemical methods (elemental
analysis, powder X-ray diffraction, IR spectroscopy). According to X-ray diffraction data (CCDC no.
2220597), zinc coordination environment in the crystal structure of I corresponds to a distorted trigonal
bipyramid. The ligand HL is monodentate and is coordinated via tetrazolate ring nitrogen. The stability of
complex I was studied by NMR spectroscopy in DMSO. The cytotoxic properties of the compound were
assessed against HepG-2 (hepatocellular carcinoma) and MRC-5 (noncancerous human fibroblasts) cells.
Complex I exhibits weak cytotoxic properties in the studied concentration range (1–100 μM).

About the authors

E. A. Ermakova

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

Email: lisalider@ngs.ru
Россия, Новосибирск

Yu. A. Golubeva

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

Email: lisalider@ngs.ru
Россия, Новосибирск

K. S. Smirnova

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

Email: lisalider@ngs.ru
Россия, Новосибирск

L. S. Klyushova

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

Email: lisalider@ngs.ru
Россия, Новосибирск

I. V. El’tsov

Novosibirsk National Research State University, Novosibirsk, Russia

Email: lisalider@ngs.ru
Россия, Новосибирск

E. V. Lider

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

Author for correspondence.
Email: lisalider@ngs.ru
Россия, Новосибирск

References

  1. Vallee B.L., Auld D.S. // Proc. Natl. Acad. Sci. USA. 1990. V. 87. № 1. P. 220.
  2. Ostrovskii V.A., Koldobskii G.I., Trifonov, R.E. Comprehensive Heterocyclic Chemistry III / Eds. Elsevier. Oxford, 2008. P. 259.
  3. Ostrovskii V.A., Trifonov R.E., Popova E.A. // Russ. Chem. Bull. 2012. V. 61. № 4. P. 768.
  4. Dofe V.S., Sarkate A.P., Kathwate S.H. et al. // Heterocycl. Commun. 2017. V. 23. № 4. P. 325.
  5. Chohan Z.H., Supuran C.T., Scozzafava A. // J. Enzyme Inhib. Med. Chem. 2008. V. 19. № 1. P. 79.
  6. Brand S.R., Degenhardt T.P., Person K. et al. // Am. J. Obstet. Gynecol. 2017. V. 217. № 6. P. 715.
  7. Hoekstra W.J., Hargrove T.Y., Wawrzak Z. et al. // Antimicrob. Agents Chemother. 2015. V. 60. № 2. P. 1058.
  8. Gonzalez-Lara M.F., Sifuentes-Osornio J., Ostrosky-Zeichner L. // Drugs. 2017. V. 77. № 14. P. 1505–1518.
  9. Warrilow A.G.S., Parker J.E., Price C.L. et al. // Antimicrob. Agents Chemother. 2016. V. 60. № 8. P. 4530–4538.
  10. May B.C.H., Abell A.D. // Tetrahedron Lett. 2001. V. 42. № 33. P. 5641.
  11. May B.C.H., Abell A.D. // Perkin Trans. 2002. V. 2. № 2. P. 172.
  12. Popova E.A., Protas A.V., Trifonov R.E. // Anticancer. Agents Med. Chem. 2017. V. 17. № 14. P. 1856.
  13. Romagnoli R., Baraldi P.G., Salvador M.K. et al. // J. Med. Chem. 2012. V. 55. № 1. P. 475.
  14. Jedhe G.S., Paul D., Gonnade R.G. et al. // Bioorganic Med. Chem. Lett. 2013. V. 23. № 16. P. 4680.
  15. Beale T.M., Allwood D.M., Bender A. et al. // ACS Med. Chem. Lett. 2012. V. 3. № 3. P. 177.
  16. Subba Rao A.V., Swapna K., Shaik S.P. et al. // Bioorganic Med. Chem. 2017. V. 25. № 3. P. 977.
  17. Mohite P.B., Bhaskar V.H. // Int. J. PharmTech Res. 2011. V. 3. № 3. P. 1557.
  18. Eremina J.A., Smirnova K.S., Klyushova L.S. et al. // J. Mol. Struct. 2021. V. 1245. P. 131024.
  19. Bruker Apex3 Software Suite: Apex3, SADABS-2016/2 and SAINT. Version 2018.7-2. Madison (WI, USA): Bruker AXS Inc., 2017.
  20. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. P. 3.
  21. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.

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Copyright (c) 2023 Е.А. Ермакова, Ю.А. Голубева, К.С. Смирнова, Л.С. Клюшова, И.В. Ельцов, Е.В. Лидер