P7C3 for Health & Longevity - Quick Reference Sheet

P7C3 for Health & Longevity

Created on 10/11/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5.5 – Audit

P7C3 is a laboratory-made molecule, neither supplement nor licensed medicine, developed to keep nerve cells alive. No person has knowingly received it in a published study. Treated animals consistently kept more nerve cells, but when the broader idea was tested in people using a widely sold nutrient, those taking it fared worse than placebo. For longevity-focused adults, an open research story: no dose, safety record or approved product for humans. (Full Review)

Protocol

No established human regimen
None defined
No human dose, frequency, duration or route; animal mg/kg figures cannot be validly converted.
Longest primate regimen tested
10 mg/kg/day orally, 38 weeks
P7C3-A20 in rhesus monkeys; an animal regimen, not a human dose.
Rodent dose range tested
1–10 mg/kg/day
Mouse assays; liver studies used 20 mg/kg/day. Not human doses.
Time to effect
New-neuron survival
5–15 days
Of dosing in rodents; unknown in humans.
Recovery after brain injury
About 30 days
Of treatment in rodents; unknown in humans.
Bone changes
Weeks to months
In rodents; unknown in humans.

Benefits

Contraindications
  • Everyone outside a regulated clinical trial
  • Active or recently treated cancer
  • Pregnancy or breastfeeding
  • Children and adolescents
  • Hepatic (liver) impairment
Key Interactions
  • CYP2C19 substrates (theoretical): clopidogrel, omeprazole, escitalopram, voriconazole (caution)
  • CYP1A2 substrates (theoretical): caffeine, theophylline, clozapine, tizanidine (caution only)
  • Over-the-counter medications (theoretical): omeprazole, esomeprazole, paracetamol (acetaminophen) (monitor)
  • Glucose-lowering drugs and supplements (theoretical): insulin, sulfonylureas (glipizide, glibenclamide), glucagon-like peptide-1 agonists (semaglutide), berberine (caution)
  • Vitamin B3 forms (theoretical, additive): nicotinamide, nicotinamide riboside, nicotinamide mononucleotide, niacin (caution)
  • NAMPT inhibitors (theoretical, opposing): FK866 (avoid)
  • Cytotoxic chemotherapy (theoretical): monitor
  • Opioids (theoretical): caution only

Risk & Side Effects

  • High:
  • Medium:
  • Low:
  • Speculative: Nerve-fibre toxicity above a narrow concentration; unresolved effect on tumour biology; suppression of inflammatory immune cells; interference with drug-metabolising enzymes; off-target receptor binding; possible lowering of blood glucose

Monitoring

Marker Target Why
Blood NAD⁺ (energy-transfer coenzyme) metabolite panel No established target; track change from own baseline Expected to change; direct pathway output
ALT (alanine aminotransferase), with AST (aspartate aminotransferase) and bilirubin ALT 7–56 U/L Safety check; cleared by the liver, a rise would pause or stop use
Complete blood count with differential Haemoglobin 13.5–17.5 g/dL (men), 12.0–15.5 g/dL (women); neutrophils 1.5–8.0 ×10⁹/L Safety check; a falling count would stop use
Fasting glucose 70–99 mg/dL Expected to change; safety check for glucose falling too low
Plasma p-tau217 (a phosphorylated form of the tau protein) No established target; track change from own baseline Expected to change where brain injury or Alzheimer-type pathology is present

Cadence: No human monitoring protocol exists; first-in-human logic: baseline, 1, 4 and 12 weeks, then every 3–6 months; earlier if any new symptom.

Qualitative Assessment

  • Memory and word-finding in daily tasks, recorded in a diary
  • Mood and motivation
  • Physical function: grip, stair climbing, walking distance
  • Any new numbness, tingling or burning in hands and feet