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Am J Physiol 272:G943G953

Sage J, Mulligan GJ, Attardi LD, Miller A, Chen S, Williams B et al

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In this work, small molecule fragments obtained by X-ray crystallography are ligated and partially optimized as non-covalent, and orally bioavailable inhibitors of TGR

To this end, we synthesized peptides 1910, 2009, 2010, and 1913 with substitutions at these positions (Table 1)

213 Kapoor et al illustrated that naringin treatment on endometrial cells significantly inhibited the expression of the Nrf2 protein and its downstream HO-1 and NQO1