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In heterodimeric GST complexes such as those formed by the cytosolic mu and alpha classes, however, the cleft between the two subunits is home to an additional high-affinity nonsubstrate xenobiotic binding site, which may account for the enzymes' ability to form heterodimers

By specifically binding to cardiolipin to form a stable complex, it not only enhances the damage resistance of the mitochondrial membrane, effectively defending against the invasion of -amyloid toxic oligomers, but also optimizes the efficiency of the electron transport chain, reducing the generation of reactive oxygen species at the source.Concurrently, it upregulates the activity of endogenous antioxidant enzymes, alleviates oxidative damage to neuronal membranes and organelles, significantly mitigates the neurotoxicity of -amyloid, and inhibits further expansion of fibrillar plaques

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Legal Status CJC-1295 is currently classified as a research chemical with no formally recognized use