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BiologicalX

Comparison

Nicotinamide Riboside vs Rapamycin

Side-by-side of Nicotinamide Riboside and Rapamycin. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

Nicotinamide Riboside

  • Most-studied NAD+ precursor in human trials; the original Niagen formulation by Chromadex
  • Plasma NAD+ rises 30-60% at 250-1,000 mg/day across multiple human PK trials
  • Martens 2018 reported reduced BP and arterial stiffness at 500 mg/day for 6 weeks
  • Dollerup 2018 found no insulin sensitivity change despite plasma NAD+ rise
  • Tissue NAD+ rise inconsistent; hard clinical endpoints not yet measured
  • Larger human safety database than NMN; comparable mechanistic effects

Rapamycin

  • Inhibits mTORC1 signaling by binding FKBP12, reducing protein synthesis and relieving autophagy suppression
  • ITP mouse program reproduced lifespan extension of ~10 to 25% across multiple genetic backgrounds and sexes
  • Mannick trials showed improved influenza vaccine response in elderly adults using analogs of rapamycin
  • PEARL human trial reported acceptable safety at 5 to 10 mg weekly with some functional and lean-mass signals
  • Common dose-limiting adverse effects include stomatitis, acne-like rash, and mildly elevated lipid markers
  • CYP3A4 substrate: grapefruit, ketoconazole, and clarithromycin substantially raise rapamycin exposure

Side-by-side

Attribute Nicotinamide Riboside Rapamycin
Category supplement pharmaceutical
Also known as NR, Niagen, nicotinamide riboside chloride Sirolimus, Rapamune
Half-life (hr) 8 62
Typical dose (mg) 500 6
Dosing frequency daily, typically morning weekly (longevity protocols); daily for transplant indication
Routes oral oral
Onset (hr) 1 1
Peak (hr) 4 2
Molecular weight 255.25 914.17
Molecular formula C11H15N2O5 C51H79NO13
Mechanism NAD+ precursor via salvage pathway. Phosphorylated to NMN by nicotinamide riboside kinase (NRK), then converted to NAD+. Substrate for sirtuins, PARPs, and CD38. Binds FKBP12, and the resulting complex inhibits mTORC1, reducing protein synthesis and autophagy suppression downstream of nutrient and growth-factor signaling.
Legal status OTC dietary supplement Prescription only (off-label for longevity)
WADA status allowed allowed
DEA / Rx OTC supplement Rx only (not a controlled substance)
Pregnancy Insufficient data at supplement doses Not recommended
CAS 1341-23-7 53123-88-9
PubChem CID 439924 5284616
Wikidata Q3343054 Q410174

Safety profile

Nicotinamide Riboside

Common side effects

  • mild GI upset (rare)
  • headache (rare)

Contraindications

  • pregnancy / lactation (insufficient data)
  • active cancer (theoretical, no contraindicating data)

Interactions

  • pterostilbene: complementary sirtuin pathway (Basis combination)(minor)
  • TMG (trimethylglycine): methylation support during high NAD+ precursor dosing(minor)

Rapamycin

Common side effects

  • mouth ulcers (stomatitis)
  • acne-like rash
  • GI upset
  • altered lipid panel
  • delayed wound healing

Contraindications

  • active infection
  • severe hepatic impairment
  • planned surgery (delayed wound healing)
  • pregnancy
  • live vaccines within dosing window

Interactions

  • strong CYP3A4 inhibitors (ketoconazole, clarithromycin, grapefruit): substantially raises rapamycin levels, toxicity risk(major)
  • strong CYP3A4 inducers (rifampin, St John's wort): lowers rapamycin levels, reduced effect(major)
  • ACE inhibitors: increased risk of angioedema(moderate)
  • live vaccines: reduced vaccine efficacy due to immunosuppression(major)

Which Should You Take?

Nicotinamide Riboside comes out ahead for most readers on the criteria we weight: 3 catalogued goals, OTC dietary supplement, oral dosing, with a Tier-A outcome catalogued. Rapamycin is the right call when one of the conditionals below applies.

Edge case: If you want to avoid prescription-only, Nicotinamide Riboside is the more accessible choice.

Default choice: Nicotinamide Riboside. Lower friction to source, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for Rapamycin only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between Nicotinamide Riboside and Rapamycin?

Nicotinamide Riboside and Rapamycin differ in category (supplement vs pharmaceutical), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, Nicotinamide Riboside or Rapamycin?

Nicotinamide Riboside half-life is 8 hours; Rapamycin half-life is 62 hours.

Can you stack Nicotinamide Riboside with Rapamycin?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

Go deeper