Compound Reference

NAD+

Nicotinamide Adenine Dinucleotide — Essential Coenzyme

NAD+ molecular structure
Molecular structure — illustrative reference.

Class

Nicotinamide Adenine Dinucleotide — Essential Coenzyme

Molecular Weight

663.4 Da

Half-life

Cellular turnover ~1 hour; systemic varies

Purity

≥98% (HPLC)

Form

Lyophilized powder

Storage

Lyophilized, protected from light and moisture at −20°C

Reconstitution

Sterile water or PBS (pH 7.4)

Mechanism of action

NAD+ is an essential coenzyme found in all living cells, participating in hundreds of metabolic redox reactions as an electron carrier. In longevity and cellular health research, NAD+ serves as a substrate for Sirtuins (SIRT1–7, NAD+-dependent deacetylases), PARP enzymes (DNA damage repair), and CD38/CD157 (cyclic ADP-ribose signaling). NAD+ levels decline markedly with age — by 50%+ in many tissues between young adulthood and middle age.

⚠️ For Research Use Only — described exclusively for in vitro and laboratory research by qualified researchers. Not for human or veterinary use. Informational only; does not constitute medical advice or imply efficacy in humans.

Research highlights

−50%

Age-related NAD+ decline in many tissues

SIRT1

Sirtuin activation: DNA repair, mitochondrial function

PARP

DNA damage repair enzyme substrate

Muscle

Improved function in aged mouse models

Research notes

  • Age-related decline: NAD+ levels fall 50%+ between young adulthood and middle age in animal models of aging.
  • Sirtuin activation: SIRT1 and SIRT3 activation linked to improved mitochondrial biogenesis, reduced inflammation, and enhanced DNA repair.
  • Muscle function: Aged mice treated with NAD+ precursors showed improved muscle strength, endurance, and reduced fatigue.
  • Neuroprotection: Neuronal models show NAD+ replenishment protects against degeneration and supports axonal integrity.
  • PARP activation: Adequate NAD+ supports genomic stability under oxidative and genotoxic stress conditions.

For Qualified Researchers

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