Chemistry & Structure

Acetylation

Acetylation is a chemical modification in which an acetyl group (CH3CO-) is added to the free amino group at a peptide's N-terminus. This eliminates the positive charge of the terminal amine and blocks recognition by aminopeptidases.

N-terminal acetylation is one of the most common modifications in synthetic research peptides. TB-500 (Thymosin Beta-4 analog) features an acetylated N-terminus (Ac-SDKP...), which contributes to its metabolic stability.

Acetylation can also occur on lysine side chains (epsilon-amino groups), which is a critical post-translational modification in protein biology. Sirtuin enzymes, which use NAD+ as a cofactor, catalyze deacetylation of lysine residues — a process central to research on NAD+ and cellular regulation.

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Research Use Only

FOR RESEARCH USE ONLY. Products sold by Healthy Aminos are intended strictly for in-vitro research and laboratory use. Not for human or animal consumption. Not FDA approved. By purchasing from Healthy Aminos, the buyer acknowledges that these products are not intended to diagnose, treat, cure, or prevent any disease. All products are sold as reference standards and research chemicals only.