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The peptides can be designed for transcription factors, specific receptors, and tumor suppressor proteins to disrupt the regulation of timing/rate of gene expression and cell cycle progression

The molecule contains a cysteine-linked disulfide bridge that constrains the peptide into a cyclic conformation, an important feature for maintaining its signaling profile in biochemical and adipocyte-based assays

By blocking NNMT, 5-amino-1MQ stimulates an increase in nicotinamide adenine dinucleotide (NAD+), a cofactor that is central to cellular metabolism, thereby increasing metabolic rate and activating a gene called sirtuin-1 (SIRT1)

This reaction catalyzes the hydroxylation of hundreds of structurally diverse drugs, whose only common characteristic is high lipid solubility

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