Synthesis, Structure, and Study of the Cytotoxic Activity of Zinc(II) Complex with 5-Benzyltetrazole and 1,10-Phenanthroline
- 作者: Ermakova E.A.1, Golubeva Y.A.1, Smirnova K.S.1, Klyushova L.S.2, El’tsov I.V.3, Lider E.V.1
 - 
							隶属关系: 
							
- Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia
 - Research Institute of Molecular Biology and Biophysics, Federal Research Center of Fundamental and Translational Medicine, Novosibirsk, Russia
 - Novosibirsk National Research State University, Novosibirsk, Russia
 
 - 期: 卷 49, 编号 9 (2023)
 - 页面: 582-589
 - 栏目: Articles
 - URL: https://vietnamjournal.ru/0132-344X/article/view/667484
 - DOI: https://doi.org/10.31857/S0132344X22600631
 - EDN: https://elibrary.ru/WAENNY
 - ID: 667484
 
如何引用文章
详细
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).
关键词
作者简介
E. Ermakova
Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia
														Email: lisalider@ngs.ru
				                					                																			                												                								Россия, Новосибирск						
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						
I. El’tsov
Novosibirsk National Research State University, 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
- Vallee B.L., Auld D.S. // Proc. Natl. Acad. Sci. USA. 1990. V. 87. № 1. P. 220.
 - Ostrovskii V.A., Koldobskii G.I., Trifonov, R.E. Comprehensive Heterocyclic Chemistry III / Eds. Elsevier. Oxford, 2008. P. 259.
 - Ostrovskii V.A., Trifonov R.E., Popova E.A. // Russ. Chem. Bull. 2012. V. 61. № 4. P. 768.
 - Dofe V.S., Sarkate A.P., Kathwate S.H. et al. // Heterocycl. Commun. 2017. V. 23. № 4. P. 325.
 - Chohan Z.H., Supuran C.T., Scozzafava A. // J. Enzyme Inhib. Med. Chem. 2008. V. 19. № 1. P. 79.
 - Brand S.R., Degenhardt T.P., Person K. et al. // Am. J. Obstet. Gynecol. 2017. V. 217. № 6. P. 715.
 - Hoekstra W.J., Hargrove T.Y., Wawrzak Z. et al. // Antimicrob. Agents Chemother. 2015. V. 60. № 2. P. 1058.
 - Gonzalez-Lara M.F., Sifuentes-Osornio J., Ostrosky-Zeichner L. // Drugs. 2017. V. 77. № 14. P. 1505–1518.
 - Warrilow A.G.S., Parker J.E., Price C.L. et al. // Antimicrob. Agents Chemother. 2016. V. 60. № 8. P. 4530–4538.
 - May B.C.H., Abell A.D. // Tetrahedron Lett. 2001. V. 42. № 33. P. 5641.
 - May B.C.H., Abell A.D. // Perkin Trans. 2002. V. 2. № 2. P. 172.
 - Popova E.A., Protas A.V., Trifonov R.E. // Anticancer. Agents Med. Chem. 2017. V. 17. № 14. P. 1856.
 - Romagnoli R., Baraldi P.G., Salvador M.K. et al. // J. Med. Chem. 2012. V. 55. № 1. P. 475.
 - Jedhe G.S., Paul D., Gonnade R.G. et al. // Bioorganic Med. Chem. Lett. 2013. V. 23. № 16. P. 4680.
 - Beale T.M., Allwood D.M., Bender A. et al. // ACS Med. Chem. Lett. 2012. V. 3. № 3. P. 177.
 - Subba Rao A.V., Swapna K., Shaik S.P. et al. // Bioorganic Med. Chem. 2017. V. 25. № 3. P. 977.
 - Mohite P.B., Bhaskar V.H. // Int. J. PharmTech Res. 2011. V. 3. № 3. P. 1557.
 - Eremina J.A., Smirnova K.S., Klyushova L.S. et al. // J. Mol. Struct. 2021. V. 1245. P. 131024.
 - Bruker Apex3 Software Suite: Apex3, SADABS-2016/2 and SAINT. Version 2018.7-2. Madison (WI, USA): Bruker AXS Inc., 2017.
 - Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. P. 3.
 - Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.
 
补充文件
				
			
						
						
						
						
					









