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Synthesis, Identification, Theoretical Study and Effect of Heterocyclic Compounds on the Activity of GOT and GPT Enzymes
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The present report describes the synthesis of heterocyclic compounds on creatinine ring, the synthetic route started from reaction creatinine with chloroacetyl chloride to give compound (1a). Compound (1a) react with urea/thiourea respectively to give compounds (2a-3a),Shiff bases were synthesized by the reaction compounds (2a-3a) with benzaldehyde andm- nitrobenzaldehyde, respectively to give compounds (4a-5a). Esterification of compounds (4a-5a) with α- chloroethylacetate to give compounds (6a-7a). Esters derivatives were synthesized by the reaction compounds (6a-7a) with semithiocarbazide respectivelyto give compounds (8a-9a). The compounds (8a-9a) reacts with NaOH to give compounds (10a-11a). The synthesized compounds characterized by FT-IR and1HNMR spectroscopy. Beside the experimental work, we worked theoretical study involving calculated the energies. Also this study was designed to show the effects of creatinine derivatives on the activities of some transferase enzymes such as: SGOT, and SGPT enzymes in sera.
Keywords
Creatinine, Shiff Base, FTIR, Transferase Enzymes, Dipole Moment, Spectra.
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- https://en.wikibooks.org/wiki/Human_Physiology/The_Urinary_System, 2017 (accessed 15.04.2017).
- N. N. Turner, N. Lameire, D. J. Goldsmith, C. G. Winearls, J. Himmelfarb, G. Remuzzi, W. G. Bennet, M.E. de Broe, J. R. Chapman, A. Covic, V. Jha, N. Sheerin, R. Unwin, A. Woolf, Oxford Textbook of Clinical Nephrology, fourth ed., Oxford: Oxford University Press, 2015.
- S. Gowda, P. B. Desai, S. S. Kulkarni, V. V. Hull, A. A. K. Math, S. N. Vernekar, Markers of renal function tests, North American Journal of Medical Sciences 2 (2010) 170–173.
- S. Gowda, P. B. Desai, S. S. Kulkarni, V. V. Hull, A. A. K. Math, S. N. Vernekar, Markers of renal function tests, North American Journal of Medical Sciences 2 (2010) 170–173.
- https://www.urmc.rochester.edu/encyclopedia/content.aspx?ContentTypeID=167andContentID=creatinine_ serum , 2017 (accessed 15.04.2017).
- C. S. Pundir, S. Yadav, A. Kumar, Creatinine sensors, Trends in Analytical chemistry 50 (2013) 42–52.
- M. Peake, M. Whiting, Measurement of Serum Creatinine –Current Status and Future Goals, Clin. Biochem. Rev. 27 (2006) 173 – 184.
- W. Marshall, Creatinine (serum, plasma), Association for Clinical Biochemistry(2012)1-5. http://www.acb.org.uk/Nat%20Lab%20Med%20Hbk/Creatinine.pdf.
- Vogel A.I., (1974) "A text book in practical organic chemistry" 3rd Ed Longman group limited, London, pp.389.
- Modi B.R., Vashi D.M., and Desai K.R., (1994) " Synthesis of 8- trizinylamino coumarin derivatives and their fluorescent properties" Indian Journal of Chemical Technology, Vol. 1, no.5, pp. 317-318.
- Pandeya, S., Sriram, D., Nath, G., Clercq, E., 2000. Eur. J. Med. Chem. 35, 249. 12. R. Charles Conard and A. Morris Dolliver, dibenzalacetone, Organic Syntheses, Coll., 2 (1943) 167, 12 (1932) 22.
- H. K. Salin, I. K. Jassim and S. Abdalsatar,” Synthesis and characterization of some new compounds derived from semicarbazide and 2-aminooxadiazole( monomer and polymers) and study their liquid of crystalline properties”, Journal of Al-Nahrain University , Vol.(10), No.(1), 2007, pp-18-24.
- M. Dobosz, M. Pitucha and A. Chudnicka,” reactions of cyclization of semicarbazide derivatives of 1,3-diphenyl-1,2,4-triazolin-5-thione-4-acetic acid”, Acta Poloniae Pharmaecuica Drug research, Vol.(59), No.(5), 2002, pp-371-377.
- Linweaver, H., Burke, D., 1934. The determination of enzyme dissociation constants. J. Am. Chem. Soc. 56, 658.
- J. Coates, Interpretation of Infrared Spectra, A Practical Approach, John Wiley and Sons Ltd, Chichester, 2000.
- Y. Ning, R. Ernst , Interpretation of Organic Spectra, Wiley; 1st edition, 2011.
- Satyanarayna, U., 2003. Biochemistry, second ed. Books and Allied (P) Ltd., India, p. 91.
- K. Singh, M. S. Barwa, B. P. Tyagi, Eur. J. Med. Chem. 2007,42, 394.
- K. Singh, M. Singh, B. P. Tyagi, Eur. J. Med. Chem. 2006, 41,147.
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