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Common Name(s): N-acetylcarnosine,ophthalmic anti-glycation,bioavailable carnosine

CAS Number: 56353-15-2

DESCRIPTION

What It Does: Provides carnosinase-resistant anti-glycation with superior topical bioavailability.

Why It's Used: Bioavailability-protected carnosine โ€” acetylcarnosine's n-acetyl group blocks carnosinase enzymatic hydrolysis that rapidly degrades topical carnosine in skin, providing sustained delivery of carnosine's anti-glycation and antioxidant activity at the dermal level.

How It Works: N-acetyl-beta-alanyl-l-histidine: carnosinase resistant (carnosinase requires free n-terminus). hydrolysis in cells: intracellular acetylase โ†’ carnosine released inside cell. ophthalmic: clinically studied for cataract (mark babizhayev n-acetylcarnosine eye drops). anti-glycation: same carnosine mechanisms. superior tissue penetration from acetyl group lipophilicity.

Typically Found In: Anti-glycation stable products,ophthalmic-grade anti-aging

TECHNICAL DETAILS

Primary Category: Active ingredient โ€“ signal peptide

Secondary Functions: Collagen stimulation,skin firming,anti-aging

Application Areas:

Facial Skincare

Body Care

Hair Care

Beard Care

Color Cosmetics (Makeup)

Dietary/Oral Supplements

Typical Concentration Range: 0.5%โ€“3%

SOURCING & ETHICS

Vegan Status: Yes โ€“ synthetic

Halal Status: Yes

Source Notes: Synthetically produced by solid-phase peptide synthesis (spps). may be palmitoylated for stability.

SKIN COMPATIBILITY

Irritancy Rating: 1/5 โ€“ very low

Comedogenicity Rating: 0/5 โ€“ non-comedogenic

Sensitivity Concerns: Non-irritating; suitable for all skin types.

Safe for Sensitive Skin: Yes

SAFETY & COMPATIBILITY

Safety Profile: Exceptional safety profile. ewg score: 1.

Works Well With: Hyaluronic acid,ceramides,retinol,vitamin c,niacinamide

Avoid Combining With: Avoid mixing with high-concentration ahas at same ph (may hydrolyze peptide bonds)

SCIENTIFIC NOTE

Acetylcarnosine's intracellular activation by deacetylation (cytoplasmic esterases remove the acetyl group) provides a prodrug-like intracellular activation: the acetyl group provides resistance to extracellular carnosinase (protecting during penetration) and slightly increased lipophilicity (improving sc penetration), then is cleaved inside the cell to release active carnosine exactly where its anti-glycation and antioxidant functions are needed. classic prodrug design principles applied to a natural peptide.

Last Verified: Cosing database,babizhayev n-acetylcarnosine ophthalmic studies

Primary Sources: 2026-03-12