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NAD+ (100mg / 500mg)

NAD+ is examined across mitochondrial, metabolic and longevity-focused research models.
  • purity_percentage Icon 99% Purity
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$88
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NAD+ (100mg / 500mg)
Nicotinamide Adenine Dinucleotide for Mitochondrial, Metabolic, and Aging Research

NAD+ (Nicotinamide Adenine Dinucleotide) is a critical coenzyme present in all living cells, playing a vital role in energy metabolism, redox reactions, and cellular repair mechanisms. It is widely utilized in scientific research exploring mitochondrial function, DNA repair, and age-related cellular decline.

Product Overview
Supplied in 100mg and 500mg lyophilized vials, NAD+ is synthesized at pharmaceutical-grade purity (>99%). It is a fundamental component in studies focusing on oxidative phosphorylation, NAD+/NADH balance, and sirtuin pathway activation.

Key Research Attributes:

  • Mitochondrial Support: Essential for electron transport chain function and ATP production in cellular respiration models.
  • Cellular Longevity: Investigated for its regulatory role in sirtuin activation, genomic stability, and oxidative stress resistance.
  • Metabolic Efficiency: Involved in numerous enzymatic reactions governing energy utilization and cellular adaptation.
  • Neuroprotection: Studied in models of neuronal repair, neuroinflammation, and brain aging processes.


Applications in Scientific Research

  • Studies on aging, DNA repair, and cellular senescence
  • Mitochondrial biogenesis and function models
  • Redox state and metabolic regulation experiments
  • Sirtuin pathway and NAD+-dependent deacetylase assays
  • Neurodegenerative disease mechanism research

Format and Storage
Form: Lyophilized powder
Purity: >99%
Storage: Store at -20°C in a dry, light-protected container
Reconstitution: Reconstitute with sterile water in a sterile lab setting

Disclaimer: NAD+ (100mg / 500mg) is provided strictly for scientific and laboratory research purposes only. It is not intended for human or veterinary use. Researchers must follow all applicable regulations and institutional protocols.



Chemical Makeup

Molecular Formula

  • NAD+: C21H27N7O14P2

Molecular Weight

  • NAD+: 663.4 g/mol

Structure

  • NAD+: Composed of two nucleotides joined through phosphate groups – one with an adenine base and the other with nicotinamide

Other Known Titles

  • NAD+: Nicotinamide Adenine Dinucleotide, β-NAD, NAD Oxidized Form
 

NAD+ (100mg / 500mg) is available exclusively for licensed scientific research use. All orders must adhere to our Terms and Conditions.

Purity Percentage 99% Purity
Volume 500MG
Bought This Week 55
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Nicotinamide Adenine Dinucleotide (NAD+): Effects, Benefits, and Side Effects

Nicotinamide adenine dinucleotide (NAD+) is a ubiquitous cellular coenzyme involved in energy metabolism, redox reactions, and multiple signaling pathways. Interest has grown around maintaining or restoring NAD+ levels with precursors and supplements in the context of aging, metabolic health, and cellular resilience. The sources below summarise proposed benefits, mechanisms, and reported side effects.

  • •
    Nicotinamide Riboside – Benefits, Side Effects, and Dosage
    Reviews nicotinamide riboside as a precursor, including potential metabolic and cellular benefits, dose ranges, and safety notes.
    Read more
  • •
    NAD Supplements – Benefits, Side Effects, and Efficacy
    Summarises evidence for NAD focused supplements in cellular health and aging, plus tolerability and side-effect considerations.
    Read more
  • •
    Physiological Effects of NAD Supplementation
    Discusses what occurs at the level of energy metabolism, fatigue, and general well-being when supplementing NAD related compounds.
    Read more
  • •
    NAD+ – Comprehensive Overview
    High level explanation of NAD+ roles in redox balance, sirtuin activity, DNA repair, and considerations around supporting its levels.
    Read more
  • •
    NADH – Uses, Side Effects, and More
    Covers potential applications of NADH, its relationship to cellular energy production, and documented side effects.
    Read more
  • •
    Maintaining NAD+ for Healthy Aging
    Outlines how preserving NAD+ status may support metabolic health, mitochondrial function, and resilience with age.
    Read more
  • •
    Health Benefits of NAD+ in Cellular Biology
    Explores NAD+ involvement in cellular signaling, repair pathways, and possible implications in chronic disease research.
    Read more
  • •
    NAD Supplementation – Claimed Benefits and Evidence
    Reviews marketed benefits for NAD oriented supplements, current human data, and side effect reports.
    Read more
  • •
    Nicotinamide Mononucleotide (NMN) – Background and Research
    Summarises NMN as a precursor compound, its role in NAD+ biosynthesis, and emerging research interest.
    Read more
  • •
    Health Benefits of Nicotinamide Adenine Dinucleotide
    Discusses NAD+ involvement in metabolism, aging biology, and considerations around supportive strategies.
    Read more
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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.
Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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