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Like many emerging therapies, BPC-157 exists in an area where scientific interest has moved faster than the clinical evidence
"Conformational changes on substrate binding to methylmalonyl CoA mutase and new insights into the free radical mechanism"
Its most distinctive physicochemical property is hydrolytic stability at low pH, unlike almost every peptide of comparable length, BPC-157 resists degradation in human gastric juice, a characteristic emphasised throughout the published work of Sikiric and colleagues (Curr Med Chem, 2012)
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