Abstract
Mixed ligand vanadyl(II) complexes of orotic acid and six different amino acids (isoleucine, threonine, proline, phenylalanine, lysine, and glutamine) have been synthesized. Vanadyl(II) orotate mixed ligand complexes are studied on the basis of conductivity, FTIR, UV-Vis, TG-DTG-DTA, magnetic moments, solid powder XRD, SEM, and TEM measurements. These non-electrolyte complexes are of 1 : 1 : 1 stochiometry. The major goal of this article is design and synthesis of new insulin alternative anti-diabetic drug. The insulin hormone and blood glucose level, lipid profile, liver and kidney functions, and superoxide dismutase antioxidant (SOD) are the factors to identify efficiency of the new synthesized compounds as antidiabetic drug agents.
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Bolkent, S., Bolkent, S., Yanardag, R., and Tunali, S., Diabetes Res. Clin. Pract., 2005, vol. 70, p. 103. https://doi.org/10.1016/j.diabres.2005.02.003
Zhang, H., Yi, Y., Feng, D., Wang, Y., and Qin, S., Evidence Based Complement Altern Med., 2011, vol. 69, p. 67. https://doi.org/10.1155/2011/691067
Chan, S.-Y., Ou, S.-M., Chen, Y.-T., and Shih, C.-J., Int. J. Cardiology, 2016, vol. 218, p. 170. https://doi.org/10.1016/j.ijcard.2016.05.062
Harper, E., Forde, H., Davenport, C., Rochfort, K.D., Smith, D., and Cummins, P.M., Vascular Pharmacology, 2016, vol. 82, p. 30. https://doi.org/10.1016/j.vph.2016.02.003
Zha, M.Q., Bing, Y., and Li, X., Synth. React. Inorg. Met.-Org. Chem., 2010, vol. 40, p. 447. https://doi.org/10.1080/15533174.2010.494272
Erer, H., Yesilel, O.Z., Darcan, C., and Buyukgungor, O., Polyhedron, 2009, vol. 28, p. 3087. https://doi.org/10.1016/j.poly.2009.06.052
Coats, A.W., and Redfern, J.P., Nature, 1964, vol. 201, p. 68. https://doi.org/10.1038/201068a0
Horowitz, H.W., and Metzger, G., Anal. Chem., 1963, vol. 35, p. 1464. https://doi.org/10.1021/ac60203a013
Hounsom, L., Horrobin, D., Tritschler, H., Corder, R., and Tomlinson, D., Diabetologia, 1998, vol. 41, p. 839. https://doi.org/10.1007/s001250050
Hussain, A.M., Am. En. J. Med. Sci., 2011, vol. 4, p. 84.
Siddiqui, M.R., Taha, A., Moorthy, K., Hussain, M.E., Basir, S.F., and Baquer, N.Z., J. Biosci., 2005, vol. 30, p. 483. https://doi.org/10.1007/BF02703722
Stone, S.H., Science, 1954, vol. 119, p. 100. https://doi.org/10.1126/science.119.3081.100
Woodhead, O., Otton, P., and Spake, L., Clin. Pharmacol., 1974, vol. 21, p. 11.
Carleton, H.M., Carleton’s Histological Technique, 4 ed., London: Oxford University Press, 1967.
Snedecor, G.W. and Cochran, W.G., Statistical Methods, 8 ed., Ames Iowa State University, 1982.
Refat, M.S., J. Mol. Struct., 2007, vol. 842, p. 24. https://doi.org/10.1016/j.molstruc.2006.12.006
Lever, A.B.P., Inorganic Electronic Spectroscopy, Amsterdam: Elsevier, 1986.
Valentina, U., Felicia, B.S., Victoria, A., Corina-Cristina, A., Mihaela, B., Rodica, O., and Dana, M., Molecules, 2010, vol. 15, p. 1578. https://doi.org/10.3390/molecules15031578
Nakamoto, K., Infrared and Raman Spectra of Inorganic and Coordination Compounds, New York: Wiley-Interscience, 1978.
Sandhu, G.K. and Verma, S.P., Polyhedron, 1987, vol. 6, p. 587. https://doi.org/10.1016/S0277-5387(00)81029-3
Husseiny, E.I., and Diefallah, M., Thermochim Acta, 1992, vol. 202, p. 1. https://doi.org/10.1016/0040-6031(92)85144-K
Miyauchi, A. and Okabe, T.H., Materials Transactions, 2010, vol. 51, p. 1102. https://doi.org/10.2320/matertrans.M2010027
Bolkent, S., Bolkent, S., Yanardag, R., and Tunali, S., Diabetes Res Clin Pract., 2005, vol. 70, p. 103. https://doi.org/10.1016/j.diabres.2005.02.003
Braunwald, Evaluation of liver function. in Harrison’s Principles of Internal Medicine, Braunwald, E. et al., Eds., New York: McGraw-Hill, 2001, p. 1711.
Sh, A.A. and Zari, T.A., Boletin Latinoamericanoy del Caribe de Plantas Medicinales y Aromaticas, 2009, vol. 8, p. 86.
Edwards, N.L., Crystal Deposition Diseases, in Cecil Medicine, Goldman, L. and Schafer, A.I., Eds., 24th ed., Philadelphia: Saunders Elsevier, 2011, p. 281.
Butt, A.A., Michaels, S., Greer, D., Clark, R., Kissinger, P., and Martin, D.H., AIDS Read, 2002, vol. 12, p. 317.
Gad, Z.M., Ehssan, A.N., Ghiet, H.M., and Wahman, F.L., Int. J. Diabetes Metab., 2010, vol. 18, p. 132.
Wu, D. and Cederbaum, I., Alcohol Res Health., 2003, vol. 27, p. 277.
Rajasekaran, S., Sivagnanam, K., and Subramanian, S., Biol. Trace Elem. Res., 2005, vol. 108, p. 185. https://doi.org/10.1385/BTER:108:1-3:185.
Tunali, S., and Yanardag, R., Pharm Res., 2006, vol. 53, p. 271. https://doi.org/10.1016/j.phrs.2005.12.004
Eddouks, M., Lemhadri, A., and Michel, J.B., J. Ethnopharmacol., 2005, vol. 98, p. 345. https://doi.org/10.1016/j.jep.2005.01.053
Ahmadi, S., Karimian, S., Sotoudeh, M., and Bahadori, M., Med. J. Islam Repub. Iran, 2002, vol. 16, p. 173.
Ramesh, B. and Pugalendi, K.V., J. Med. Food, 2006, vol. 9, p. 562. https://doi.org/10.1089/jmf.2006.9.562
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This work was funded by the Deanship of Scientific Research at Princess Nourah bint Abdulrahman University, through the Research Groups Program (grant no. RGP-1440-0003).
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Al-Wasidi, A.S., Al-Jafshar, N.M., Al-Anazi, A.M. et al. Synthesis, Characterization, and Anti-Diabetic Therapeutic Activity of New Vanadyl(II) Complexes with Orotic Acid and Different Amino Acids Mixed Ligands. Russ J Gen Chem 89, 2121–2128 (2019). https://doi.org/10.1134/S1070363219100219
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DOI: https://doi.org/10.1134/S1070363219100219