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First identified as a potential neuroprotective agent, in 2008, by researchers in Germany, [20] 9-me-BC was initially found to be of interest due to its ability to upregulate tyrosine hydroxylase, the enzyme responsible for converting the amino acid L-theanine into the dopamine precursor, L-DOPA

[29] [30] [31] Similar attacks on arachidonic acid produce a far larger set of products including various isoprostanes, hydroperoxy- and hydroxy- eicosatetraenoates, and 4-hydroxyalkenals

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