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All peptides
Research vial labelled NAD+, a Mitochondrial and metabolic peptide studied in preclinical and clinical literature

NAD+

Wide interest in NAD biology, with most clinical work on oral precursors rather than injected NAD+ itself.

Flushing on fast administration is consistently reported.

General profile

Class
Mitochondrial and metabolic
Evidence
Mixed or moderate evidence
Studied dose range
50–100 mg
Frequency in protocols
3–5× weekly
Route
Subcutaneous, slow push
Half life
Short, rapidly metabolised
Reconstitution
5 mL bacteriostatic water per 500 mg vial
Storage
Refrigerated, ~30 days

Timing and cycling in the literature

Usually dosed in the morning window

Three to five times weekly

Administration is uncomfortable and commonly causes flushing, so a slow morning push is easier to tolerate. Late dosing is frequently reported as sleep-disrupting.

Reported cycle: 4 weeks on, 4 weeks off

Most clinic protocols are short intensive blocks followed by a long gap, because tolerance to the flushing and the cost both climb.

Watch for: Chest tightness and flushing during the push, which is dose rate dependent. Slow down rather than pushing through.

What it conflicts with

Three separate questions, kept separate. A hard stop means the mechanisms must not run together at all and timing does not fix it. A syringe rule means the same day is fine but one barrel is not. Redundancy is not dangerous, it is paying twice to hit one target.

No named pair conflicts are on file for this compound. That is missing data, not clearance: with no compatibility data the default is separate syringes, and you still introduce one new compound at a time.

Most syringe compatibility claims here are practice and expert consensus, not peer reviewed mixing studies. A clear liquid after mixing does not prove the compounds are still active, and cloudiness, particles or gelling means discard. Active cancer, pregnancy, major cardiac care and heavy immunosuppression override every stack preference on this page.

See how NAD+ fits your week

The injection scheduler spaces doses using the clinical timing data, flags the pairs above before you draw them, and tells you why.

Model this in the injection scheduler

The studies

Human trials: Small trials of nicotinamide riboside and NMN on NAD levels, with modest functional endpoints.

Open questions: Injected NAD+ protocols are almost entirely clinic practice rather than trial data.

Published papers

Indexed from Europe PMC and refreshed weekly. Each link opens the paper itself.

Search the full literature