Side-by-side comparison of mechanisms, dosing, interactions, and stacking potential.
| NAC (N-Acetyl Cysteine) | NMN (Nicotinamide Mononucleotide) | |
|---|---|---|
| Category | Supplements | Supplements |
| Standard Dose | 600-1200mg daily | 500-1000mg daily |
| Timing | On empty stomach for best absorption, 30 min before meals. Split doses if >600mg. | Morning on empty stomach. Sublingual absorption bypasses first-pass metabolism. |
| Cycle Duration | Cycle 8 weeks on, 2 weeks off (to avoid potential downregulation of endogenous GSH production) | ongoing |
| Evidence Level | strong_human | moderate_human |
NAC is a precursor to L-cysteine, the rate-limiting substrate for glutathione (GSH) synthesis via glutamate-cysteine ligase. It directly replenishes intracellular GSH, the master endogenous antioxidant. NAC also modulates glutamatergic neurotransmission by stimulating the cystine-glutamate antiporter (system Xc-), influencing extrasynaptic glutamate levels. Additionally, it acts as a mucolytic by cleaving disulfide bonds in mucus glycoproteins.
600-1200mg daily
On empty stomach for best absorption, 30 min before meals. Split doses if >600mg.
Cycle 8 weeks on, 2 weeks off (to avoid potential downregulation of endogenous GSH production)
NMN is a direct biosynthetic precursor to NAD+ via the salvage pathway enzyme nicotinamide phosphoribosyltransferase (NAMPT). Elevated NAD+ activates sirtuins (SIRT1-7), PARP DNA repair enzymes, and CD38/CD157 signaling. SIRT1 activation deacetylates PGC-1alpha (mitochondrial biogenesis), FOXO transcription factors (stress resistance), and NF-kB (anti-inflammatory). NMN also enters cells via the Slc12a8 transporter, recently identified in the gut.
500-1000mg daily
Morning on empty stomach. Sublingual absorption bypasses first-pass metabolism.
ongoing
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