An Interaction Study of Chloro and Alkyl Substituted Benzylamine with DPPH● through UV Spectrophotometric and Physicochemical Methods at T = (298.15, 303.15 and 308.15) K
- 1 School of Chemical Sciences, Central University of Gujarat, Gandhinagar, India
- 2 School of Chemical Sciences, Central University of Gujarat, Gandhinagar, India
- 3 School of Chemical Sciences, Central University of Gujarat, Gandhinagar, India
Abstract
Radical scavenging activity (RSA) of chloro and methyl substituted benzylamine derivatives (BADs) has been studied using 1, 1-diphenyl-2-picrylhydrazyl free radical (DPPH?) through spectrophotometric and physico - chemical techniques at T = (298.15, 303.15 and 308.15) K. New experimental data on the density, sound velocity, isentropic and apparent molal compressibility of selected BADs + DPPH ● solutions as a function of temperature and concentration are reported. The results are discussed with regards to structure-activity relationship (SAR) principles of BADs. The relative deviations in RSAs varied with structural potentials of BADs which were ana lyzed by making a comparative study for both the spectrophotometric and physicochemical results.
- F. Pourmorad, S. J. Hosseinimehr and N. Shahabimajd, African Journal of Biotechnology, Vol. 5, 2006, p. 1142.
- N. C. Cook and S. Samman, The Journal of Nutritional Biochemistry, Vol. 7, 1996, pp. 66-76. http://dx.doi.org/10.1016/0955-2863(95)00168-9
- D. Ku-mar, S. Kumar, J. Singh, Narender, Rashmi, B. D. Vashistha and N. Singh, Journal of Young Pharmacists, Vol. 2, 2010, pp. 365-368. http://dx.doi.org/10.4103/0975-1483.71627
- O. I. Aruoma, Free Radical Biology & Medicine, Vol. 20, 1996, p. 675. http://dx.doi.org/10.1016/0891-5849(95)02110-8
- B. Halliwell, Biochemical Pharmacology, Vol. 49, 1995, p. 1341. http://dx.doi.org/10.1016/0006-2952(95)00088-H
- J. Vaya and M. Aviram, Curr. Med. Chem.-Immunol. Endocr. Metab. Agents, Vol. 1, 2001, p. 99. http://dx.doi.org/10.2174/1568013013359168
- M. E. Camire, M. P. Dougherty and J. L. Briggs, Cereal Chemistry, Vol. 82, 2005, pp. 666-670. http://dx.doi.org/10.1094/CC-82-0666
- I. F. F. Benzie and J. J. Strain, Analytical Biochemistry, Vol. 239, 1996, pp. 70-76. http://dx.doi.org/10.1006/abio.1996.0292
- A. Dapkevicius, R. Venskutonis, T. A. Beek and J. P. H. Linssen, Journal of the Science of Food and Agriculture, Vol. 77, 1998, p. 140. http://dx.doi.org/10.1002/(SICI)1097-0010(199805)77:1 3.0.CO;2-K
- B. H. J. Bielski, Journal of Physical and Chemical Reference Data, Vol. 14, 1985, pp. 1041-1091. http://dx.doi.org/10.1063/1.555739
- T. Finkel and N. J. Holbrook, Nature, London, Vol. 239, 2000, p. 408.
- C. A. Rice-Evans, N. J. Miller and G. Paganga, Free Radical Biology & Medicine, Vol. 20, No. 7, 1996, p. 933. http://dx.doi.org/10.1016/0891-5849(95)02227-9
- C. Jianguo, X. Xian, C. Xuefei, X. Jianbo and W. Quanxi, Food and Chemical Toxicology, Vol. 51, 2013, pp. 242- 250. http://dx.doi.org/10.1016/j.fct.2012.09.039
- A. Huber, P. Thongphasuk, G. Erbenc, W. D. Lehmann, S. Tuma, W. Stremmel and W. Chamulitra, Biochimica et Biophysica Acta, 2008, pp. 837-847.
- M. M. Sanaa Shanab, S. M. Soha Mostafa, A. Emad Shalaby and I. Ghada Mahmoud, Asian Pacific Journal of Tropical Biomedicine, 2012, pp. 608-615.
- R. K. Ameta, M. Singh and R. K. Kale, Journal of Coordination Chemistry, Vol. 66, 2013, pp. 551-567. http://dx.doi.org/10.1080/00958972.2013.763230