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Alkaptonuria Alkaptonuria is a rare autosomal recessive disorder caused by defects in the gene encoding an enzyme, homogentisic acid oxidase, involved in the catabolism of phenylalanine and tyrosine

doi: 10.3390/antiox8090378 38 WanJRenHWangJ

This makes MOTS-c more targeted and less likely to produce off-target gastrointestinal side effects common with metformin

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Scientific References Journal of Pharmaceutical Sciences Analysis of the antimicrobial efficacy and stability of benzyl alcohol in aqueous solutions