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During this conjugation process, an enzyme family called glutathione S-transferases (GSTs) catalyzes the physical attachment of the glutathione molecule directly to the toxic compound

The formulation combines Glycyl-L-histidyl-L-lysine copper(II) (GHK-Cu), Body Protection Compound-157 (BPC-157), Thymosin Beta-4 derivative (TB500), and the naturally occurring alpha-MSH cleavage derivative, KPV

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Both converge on reduced energy intake without sharing the same receptor target [6]