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. Author manuscript; available in PMC: 2020 Feb 1.
Published in final edited form as: Free Radic Biol Med. 2018 Dec 19;131:332–344. doi: 10.1016/j.freeradbiomed.2018.12.023

Figure 4.

Figure 4.

The formation of the methylglyoxal (MGO) conjugated metabolites of 4'-NH2-EGCG in mice. The LC chromatograms and the ESI-MS2 spectra of MGO-NH2-EGCG (m/z 528 [M-H]) (A) and N-MGO-NH2-EGCG (m/z 510 [M-H]) (B) of mouse fecal and urinary samples collected from EGCG (1) treated mice, 4'-NH2-EGCG (2) treated mice, and the sample collected from chemical incubation of 4'-NH2-EGCG (2) with MGO in phosphate buffer (pH 7.4) at 37 °C for 3 h.