Date published: 2025-9-28

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sarcosine dehydrogenase Inhibitors

Sarcosine dehydrogenase inhibitors are a class of compounds that target and inhibit the activity of sarcosine dehydrogenase, an enzyme primarily involved in the oxidative demethylation of sarcosine (N-methylglycine). Sarcosine dehydrogenase is a key component of the mitochondrial folate one-carbon metabolic pathway, which plays a role in converting sarcosine into glycine while releasing formaldehyde. This reaction is crucial in the broader context of amino acid metabolism, particularly within methylation cycles and the regulation of cellular levels of compounds like S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH). By inhibiting sarcosine dehydrogenase, these inhibitors interfere with the enzyme's ability to modulate sarcosine levels, thus potentially altering the balance of glycine and formaldehyde production, which can have downstream effects on cellular metabolic processes.

The inhibition of sarcosine dehydrogenase can lead to the accumulation of sarcosine and disruption of the folate one-carbon cycle, which could affect the methylation capacity of cells, as well as the biosynthesis of nucleotides and other methyl group donors. Inhibitors of this enzyme are of particular interest in studies exploring the regulation of metabolic fluxes in systems that depend on finely tuned methylation reactions, such as the maintenance of nucleic acid synthesis, energy production, and protein metabolism. These compounds are valuable for understanding the role of sarcosine in cellular metabolic networks and its impact on mitochondrial function, particularly in relation to oxidative stress and the production of reactive intermediates such as formaldehyde during the demethylation process.

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