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Research into 5-Amino-1MQ has showcased its ability to increase NAD+ concentrations, leading to enhanced cellular metabolism, particularly within fat cells

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To this end, we synthesized a number of permethylated quinolinium analogues[17] guided by in silico calculation of partition coefficient (clogP).[26] Addition of hydrophobic methyl group substitutions around the quinolinium scaffold (previously shown to negatively impact NNMT inhibitory activity)[17] only slightly improved membrane permeability via passive transport as indicated by the low, but non-zero, permeability values for 1,8-diMQ and 1,2,4,8-tetraMQ (Table 1)

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Song R (2016) Mechanism of metformin: a tale of two sites