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Description
Oleocanthal Oleocanthal (Oc), a dialdehydic derivative of decarboxymethyl elenolic acid bound to Tyr, ( p -HPEA-EDA) was shown in vitro to inhibit both COX-1 and COX-2, inflammatory enzymes involved in the biosynthesis of inflammatory prostaglandins in a dose-dependent manner, and to be more effective than ibuprofen in inhibiting these enzymes at equimolar concentrations [260] (see Figure 1)

This research has been supported by the National Key Research and Development Program of China (grant no

doi: 10.1016/j.leukres.2016.07.010
BPC-157 is explicitly named on the WADA Prohibited List (Section S0) since 2022

Membrane-associated LRRK2 stimulates Beclin-1 and suppresses autophagy by interacting with TAB2

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