CLASSIFICATION: METABOLIC COFACTOR / NAD+ PRECURSOR
ACTIVE SUBSTANCE: NICOTINAMIDE ADENINE DINUCLEOTIDE
FORM: LYOPHILIZED POWDER (2 ML VIAL x 500 MG)
ACTIVE HALF-LIFE: APPROX. 1–2 HOURS
DOSAGE: 100–300 MG/WEEK (RESEARCH USE)
ACNE: NO
WATER RETENTION: NO
HBR: NO
HEPATOTOXICITY: NONE
AROMATIZATION: NO
MANUFACTURER: PEPTIDE HUBS
Peptide Hubs presents its premium research-grade NAD+ 500 mg, offering the highest concentration of Nicotinamide Adenine Dinucleotide available for advanced investigative studies into cellular metabolism, mitochondrial function, and the biology of aging. NAD+ is not a peptide but a fundamental coenzyme present in every cell, crucial for over 500 enzymatic reactions, including those central to energy production (ATP synthesis), DNA repair, and cellular defense. With age and metabolic stress, NAD+ levels decline precipitously, a phenomenon linked to reduced mitochondrial efficiency, cellular senescence, and increased vulnerability to disease. Our high-dose 500 mg lyophilized powder provides researchers with a potent tool to explore the effects of NAD+ repletion on energy metabolism, exercise performance, cognitive function, and systemic rejuvenation. Sourced and manufactured under rigorous controls in a USA facility, this product represents the forefront of accessible, high-purity metabolic research compounds.
NAD+ functions as a vital electron carrier in redox reactions, shuttling electrons during the conversion of nutrients into cellular energy (ATP) within the mitochondria. Its role extends far beyond energy production. NAD+ is the required substrate for critical longevity-associated enzymes called sirtuins (SIRT1-7), which regulate gene expression, DNA repair, and stress resistance. It also fuels PARP enzymes involved in DNA repair and CD38 for calcium signaling. In research settings, elevating NAD+ levels has been associated with profound effects:
NAD+ 500 mg is typically administered via intravenous (IV) drip, intramuscular (IM), or subcutaneous (SubQ) injection in research settings, with the route significantly impacting bioavailability and effect profile. IV administration provides the most immediate and complete systemic saturation but requires specialized equipment. For laboratory studies, intramuscular or subcutaneous protocols are more common. Research dosages vary widely based on the model and objective. Common investigative ranges are between 50 mg to 500 mg per administration. For high-dose protocols, the 500 mg vial allows for efficient dosing. Reconstitution is performed with sterile bacteriostatic water or saline. For example, adding 2.5 mL to the 500 mg vial yields a concentration of 200 mg/mL. A 0.5 mL (100 mg) injection would then be drawn from this solution. Frequency can range from daily to 2-3 times per week, depending on the research design aimed at maintaining elevated NAD+ levels. Strict aseptic technique is non-negotiable.
Given its role in fundamental cellular processes, NAD+ research cycles can be highly variable. For studying acute effects on energy and recovery, short cycles of 2-4 weeks with frequent dosing may be used. For investigating longer-term impacts on gene expression and anti-aging biomarkers, cycles of 8-12 weeks or longer are common. NAD+ synergizes powerfully with other compounds that support mitochondrial health and longevity. Researchers often combine it with Epitalon 50 mg to study synergistic effects on telomere maintenance and pineal gland regulation. For comprehensive cellular protection and antioxidant support, stacking with L-Glutathione 600 mg is logical. To explore enhanced metabolic and endurance adaptations, combination with MOTS-C 10 mg, a mitochondrial-derived peptide, is a cutting-edge area of study. For research focused on tissue repair and inflammation modulation post-exercise, adding BPC 157 can create a robust recovery protocol. Furthermore, to support the structural health of joints and connective tissues under metabolic stress, Chonluten 20 mg can be incorporated into the research design.
In research models, NAD+ is generally well-tolerated as it is an endogenous molecule. However, rapid administration, particularly via IV, can cause transient side effects related to vasodilation and the flushing of metabolites. These may include a warm flushing sensation in the face and chest, mild nausea, lightheadedness, or fatigue, which typically pass within 30-60 minutes. Slower infusion rates or switching to IM/SubQ routes often mitigate these effects. There is no evidence of androgenic, estrogenic, or progestogenic activity—no acne, water retention, or HBP from hormonal mechanisms. On the contrary, it may support cardiovascular health. It is not hepatotoxic; in fact, it may support liver function. There is no aromatization or HPTA suppression. Researchers should monitor for signs of localized irritation at injection sites. The primary consideration is that high doses may temporarily alter redox state, so comprehensive metabolic monitoring is advised. This compound is strictly for controlled laboratory research.
The interest in NAD+ supplementation in research is directly tied to its central role in countering several recognized "hallmarks of aging." The age-related decline in NAD+ contributes to:
By repleting NAD+, researchers are investigating interventions that may simultaneously address multiple of these pathways, making it a cornerstone molecule in the field of geroscience and performance longevity.
The stability and potency of NAD+ are paramount for credible research. Peptide Hubs' NAD+ 500 mg is synthesized to the highest pharmaceutical standards, lyophilized to ensure long-term stability, and sealed under inert gas to prevent oxidation. Each batch is subjected to rigorous analytical testing via HPLC to confirm purity (>99%) and the absence of degradation products like nicotinamide. Mass spectrometry verifies molecular identity. This commitment to quality ensures that researchers are working with a fully active, reliable coenzyme, allowing for the generation of reproducible and meaningful data in the study of cellular energetics and longevity science.
NAD+ is the active coenzyme itself. NMN (Nicotinamide Mononucleotide) and NR (Nicotinamide Riboside) are precursors that the body must convert into NAD+. Direct NAD+ administration bypasses these conversion steps, which can be rate-limited or inefficient, especially in aged models. Research using direct NAD+ allows for the study of immediate, potent elevation of systemic NAD+ levels, whereas precursor studies focus on sustained, oral-based elevation.
Yes, this is a significant area of inquiry. Anabolic cycles can place high metabolic demands on the liver and cellular energy systems. Research into NAD+ post-cycle may explore its role in supporting hepatic detoxification pathways, replenishing cellular energy (ATP) to combat fatigue, and activating sirtuin-mediated repair processes to aid in overall systemic recovery and homeostasis. It is a non-hormonal support agent.
The "flush" is a transient vasodulatory response, often experienced as warmth, redness, and sometimes mild itching in the face and upper body. It's believed to be caused by a temporary surge in prostaglandin release as NAD+ is metabolized. It is generally harmless and subsides within an hour. Slowing the injection/infusion rate or administering an antihistamine prior to dosing in a research setting can mitigate this effect. It is not an allergic reaction.
Absolutely. The brain is an energy-intensive organ highly susceptible to declining NAD+ levels. Research into NAD+'s role in supporting neuronal mitochondrial function, reducing neuroinflammation, and activating neuroprotective sirtuins (like SIRT1 and SIRT3) is well-established. For synergistic neurocognitive research, it is often paired with nootropic peptides like Semax or mitochondrial protectants like SS-31.
The lyophilized powder is stable for 2+ years when stored in a freezer at -20°C. After reconstitution with bacteriostatic water, the solution should be used promptly for optimal potency. If necessary, it can be stored refrigerated at 2-8°C for up to 7-10 days, but researchers should note that NAD+ in solution can gradually degrade. For best research practices, reconstitute single-use aliquots immediately before administration.
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CLASSIFICATION: METABOLIC COENZYME / ANTI-AGING PEPTIDE
ACTIVE SUBSTANCE: NICOTINAMIDE ADENINE DINUCLEOTIDE (NAD+)
FORM: 2 ML VIAL x 500 MG (LYOPHILIZED POWDER)
ACTIVE HALF-LIFE: APPROX. 2–4 HOURS
DOSAGE: 100–300 MG PER INJECTION, 1–3 TIMES PER WEEK
ACNE: NONE
WATER RETENTION: NONE
HIGH BLOOD PRESSURE (HBP): UNLIKELY
HEPATOTOXICITY: NONE
AROMATIZATION: NONE
MANUFACTURER: DRAGON PHARMA
CLASSIFICATION: METABOLIC COFACTOR / NAD+ PRECURSOR
ACTIVE SUBSTANCE: NICOTINAMIDE ADENINE DINUCLEOTIDE
FORM: LYOPHILIZED POWDER (2 ML VIAL x 100 MG)
ACTIVE HALF-LIFE: APPROX. 1–2 HOURS
DOSAGE: 100–300 MG/WEEK (RESEARCH USE)
ACNE: NO
WATER RETENTION: NO
HIGH BLOOD PRESSURE (HBP): NO
HEPATOTOXICITY: NONE
AROMATIZATION: NO
MANUFACTURER: PEPTIDE HUBS
LABORATORY TESTED: VIEW LAB RESULTS
CLASSIFICATION: RECOMBINANT HUMAN GROWTH HORMONE (rHGH)
ACTIVE SUBSTANCE: SOMATROPIN
FORM: 1 PRE-FILLED PEN x 36 IU (12 MG)
ACTIVE HALF-LIFE: ~3.5 HOURS (SUBQ)
DOSAGE: 1–4 IU/DAY FOR ANTI-AGING; 4–8 IU/DAY FOR FAT LOSS OR PERFORMANCE
WATER RETENTION: POSSIBLE (DOSE DEPENDENT)
HEPATOTOXICITY: NONE
AROMATIZATION: NO
MANUFACTURER: PFIZER
CLASSIFICATION: RECOMBINANT HUMAN GROWTH HORMONE (r-hGH)
ACTIVE SUBSTANCE: SOMATROPIN (R-HGH)
FORM: 1 CARTRIDGE x 15 MG
ACTIVE HALF-LIFE: ~2–3 HOURS
DOSAGE: MEN 4-10 IU/DAY
ACNE: POSSIBLE
WATER RETENTION: POSSIBLE
HIGH BLOOD PRESSURE (HBP): MAY INCREASE VIA FLUID RETENTION
HEPATOTOXICITY: NONE TYPICAL
AROMATIZATION: NONE
MANUFACTURER: NOVO NORDISK
CLASSIFICATION: GONADOTROPIN (LH RECEPTOR AGONIST)
ACTIVE SUBSTANCE: HUMAN CHORIONIC GONADOTROPIN
FORM: 1 LYOPHILIZED VIAL x 5000 IU + PROVIDED SOLVENT
ACTIVE HALF-LIFE: ~24–36 HOURS
DOSAGE: MEN 500-1000 IU
ACNE: POSSIBLE
WATER RETENTION: POSSIBLE
HIGH BLOOD PRESSURE (HBP): MONITOR IF AT CV RISK
HEPATOTOXICITY: NONE TYPICAL
AROMATIZATION: INDIRECT
MANUFACTURER: IBSA