⬡ THIRD-PARTY HPLC TESTED⬡ >98% PURITY GUARANTEED⬡ CERTIFICATE OF ANALYSIS INCLUDED⬡ PREMIUM GRADE COMPOUNDS⬡ FAST TRACKED SHIPPING⬡ 24 PREMIUM PEPTIDES⬡ THIRD-PARTY HPLC TESTED⬡ >98% PURITY GUARANTEED⬡ CERTIFICATE OF ANALYSIS INCLUDED⬡ PREMIUM GRADE COMPOUNDS⬡ FAST TRACKED SHIPPING⬡ 24 PREMIUM PEPTIDES⬡ THIRD-PARTY HPLC TESTED⬡ >98% PURITY GUARANTEED⬡ CERTIFICATE OF ANALYSIS INCLUDED⬡ PREMIUM GRADE COMPOUNDS⬡ FAST TRACKED SHIPPING⬡ 24 PREMIUM PEPTIDES⬡ THIRD-PARTY HPLC TESTED⬡ >98% PURITY GUARANTEED⬡ CERTIFICATE OF ANALYSIS INCLUDED⬡ PREMIUM GRADE COMPOUNDS⬡ FAST TRACKED SHIPPING⬡ 24 PREMIUM PEPTIDES
HomePeptidesNAD+ 500mg
NAD+ Nicotinamide Adenine Dinucleotide 500mg
Cellular Energy
HPLC Tested
CoA Included
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Longevity

NAD+ Nicotinamide Adenine Dinucleotide 500mg

The Master Coenzyme Driving Cellular Energy, DNA Repair & Sirtuin Activation

NAD+ is the foundational coenzyme of life — found in every living cell and essential for over 500 enzymatic reactions. Its decline with age represents one of the most significant molecular events underlying the aging process, making it a critical target in longevity and metabolic science.

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Size
500mg
Purity
>98% (HPLC)
CAS
53-84-9
Form
Lyophilized Powder
Testing
Third-Party CoA
Category
Longevity

The Master Coenzyme Driving Cellular Energy, DNA Repair & Sirtuin Activation

Nicotinamide adenine dinucleotide (NAD+) has emerged from decades of relative obscurity to become one of the most important molecules in aging science. Concentrations of NAD+ fall by approximately 50% between youth and middle age, and this decline correlates with the hallmark features of metabolic dysfunction, mitochondrial deterioration, and genomic instability seen in aging tissues. Research led by pioneers like David Sinclair at Harvard has established NAD+ as the key activator of sirtuin proteins (SIRT1–7) — epigenetic regulators that govern gene expression, mitochondrial biogenesis, inflammation control, and DNA repair.

NAD+ 500mg Documented Benefits: 6 Documented Mechanisms

1

Sirtuin Pathway Activation

NAD+ is the essential substrate for SIRT1, SIRT3, and other sirtuin enzymes that regulate hundreds of age-related metabolic and epigenetic processes. Restoring NAD+ allows sirtuins to function at youthful activity levels.

2

Mitochondrial Biogenesis & Function

SIRT1 and SIRT3 activation by NAD+ drives PGC-1α expression — the master regulator of mitochondrial biogenesis — resulting in more numerous, efficient mitochondria and improved cellular energy output.

3

DNA Repair via PARP Activation

PARP enzymes that detect and repair DNA strand breaks are NAD+-dependent. Adequate NAD+ availability ensures rapid, accurate DNA repair — preventing mutation accumulation that drives cancer and aging.

4

Metabolic Rate & Insulin Sensitivity

Research in obese rodent models shows NAD+ restoration dramatically improves insulin sensitivity and metabolic rate, with implications for body composition optimization and metabolic syndrome science.

5

Neurological Protection & Cognitive Research

NAD+ supports neuron survival through sirtuin-mediated protection and PARP-mediated repair. Research in neurodegeneration models shows preservation of cognitive function with NAD+ restoration protocols.

6

Circadian Rhythm Synchronization

SIRT1 and CLOCK proteins are interdependent — NAD+ levels fluctuate circadianly and help drive the molecular clock that synchronizes metabolism, sleep cycles, and cellular maintenance windows.

How NAD+ 500mg Works: Molecular Mechanism & Pathway

NAD+ operates as a hydride ion (H-) carrier in the electron transport chain, shuttling electrons from metabolic substrates to Complex I of the mitochondria for ATP synthesis. As a signaling molecule, it serves as the rate-limiting substrate for CD38 (which depletes NAD+ with age), PARP enzymes (DNA repair), and sirtuins (metabolic regulation). The NAD+/NADH ratio acts as a cellular redox sensor that modulates transcription of hundreds of genes in response to metabolic state.

Key Highlights

  • David Sinclair (Harvard) studies show NAD+ restoration reverses vascular aging in mice
  • NMN and NR precursor studies consistently show 40–90% NAD+ tissue restoration in animal models
  • PARP knockout studies demonstrate NAD+ depletion is central to aging-related DNA damage accumulation
  • Human trials with NAD+ precursors show improvements in muscle function and metabolic markers in older adults

Ideal For

  • Aging biology and longevity science
  • Metabolic syndrome investigation
  • Mitochondrial function studies
  • Sirtuin pathway science
  • Circadian biology
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Third-party tested · CoA included

⚠ For Lab Use Only

Intended for laboratory use only. Not for human or animal consumption. Not FDA approved. Handle in appropriate lab settings only.

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