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Reported biochemical potency against human NNMT is in the low-micromolar range with cellular EC values in the low-micromolar range for suppression of 1-MNA and lipogenesis, with selectivity over related methyltransferases and NAD-salvage enzymes [1,6,7]

That role is real and well described in biochemistry

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Research study findings indicate that the fragment seems to have the capacity to amplify lipolytic sensitivity following its introduction