Abstract
2,4,6-Trichlorophenyl hydrazones 1-35 were synthesized and their in vitro antiglycation potential was evaluated. Compounds 14 (IC50 = 27.2 ± 0.00 μM), and 18 (IC50 = 55.7 ± 0.00 μM) showed an excellent activity against glycation of protein, better than the standard (rutin, IC50 = 70 ± 0.50 μM). This study thus identified a novel series of antiglycation agents. A structure-activity relationship has been studied, and all the compounds were characterized by spectroscopic techniques. © 2011 Bentham Science Publishers.
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CITATION STYLE
Mohammed Khan, K., Shah, Z., Uddin Ahmad, V., Khan, M., Taha, M., Rahim, F., … Iqbal Choudhary, M. (2012). Synthesis of 2,4,6-Trichlorophenyl Hydrazones and their Inhibitory Potential Against Glycation of Protein. Medicinal Chemistry, 7(6), 572–580. https://doi.org/10.2174/157340611797928415
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