Abstract
Two novel and two known compounds, 4-quinolylaldoxime and indole-3-aldehyde, were isolated from a reaction mixture consisting of D-glucose and L-tryptophan at physiological temperature and pH. The chemical structures of the two novel compounds were elucidated by spectroscopic analysis such as X-ray crystallography. One of the novel compound and the indole-3-aldehyde showed mutagenicity toward Salmonella typhimurium YG1024 with S9 mix. Furthermore, 4-quinolylaldoxime was detected from streptozotocin-induced diabetic rat plasma by LC-MS/MS analysis; however, the isolated compounds were not detected in rat diet extracts. To our knowledge, this is the first report in which 4-quinolylaldoxime was detected in rat plasma. These results suggest that amino-carbonyl reaction products may be formed in diabetic condition and induce genetic damage.
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Imahori, D., Matsumoto, T., Kojima, N., Hasei, T., Sumii, M., Sumida, T., … Watanabe, T. (2018). Chemical structures of novel maillard reaction products under hyperglycemic conditions. Chemical and Pharmaceutical Bulletin, 66(4), 363–367. https://doi.org/10.1248/cpb.c17-00809
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