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The fragment was named for its proposed "body protection compound" activity in early rat gastric-lesion models (Sikiric et al., 2018
In animal models the parent compound is described as relatively short-lived in plasma but with effects persisting longer than the systemic exposure window a profile the Zagreb group attributes to its stability in the gastrointestinal lumen and to downstream signaling cascades (Sikiric et al., 2018)
As deficiency deepens, it becomes more persistent
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