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Fisetin

Aliases: Fisatin

Last verified: 2026-09-23

Clinical trialsModerate evidenceSmall moleculesLow interest

The short version

A flavonoid (strawberries, apples) — the most potent natural senolytic in preclinical screens; extends mouse lifespan. RCTs ongoing (AFFIRM-Lite etc.). Status: in clinical trials. Legal supplement.

Identity & type

Molecular type
mali molekul
Origin
A flavonoid (strawberries, apples) — the most potent natural senolytic in preclinical screens; extends mouse lifespan.

Mechanism of action

Senolytic + antioxidant/anti-inflammatory action; inhibition of multiple pro-aging pathways (mTOR, NF-κB).

Dosing & routes

Official / clinical context

No approved official document exists for Fisetin. Any protocols mentioned are to be read as information, not as a recommendation.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

Trials: ~20 mg/kg/day for 2 days (intermittent); supplements 100–500 mg/day. Popular as a "safe senolytic": subtle effects on energy and joints at intermittent high doses; cheap and available.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Popular as a "safe senolytic": subtle effects on energy and joints at intermittent high doses; cheap and available.

Protocol — official vs community

Official / label

No approved use. Senolytic-flavored trials used high intermittent doses (~20 mg/kg/day for 2–3 consecutive days) extrapolated from mouse work.

  1. 01Intermittent high-dose days only

Duration: Course-based, months between courses in trials.

The intermittent pattern distinguishes senolytic intent from generic antioxidant use.

Community (anecdotal)

Either continuous low-dose (100–500 mg/day) or intermittent high-dose (1,000–2,000 mg/day ×2–3 days) 'senolytic pulse'.

Cycle:
Pulse courses every 1–6 months.
Break:
Built into the pulse schedule.

The two community patterns (chronic low vs intermittent high) reflect two different theories of fisetin — nobody knows which is right.

Human evidence

Mayo Clinic RCT program; preclinical lifespan extension ~10%.

Preclinical evidence

Preclinical literature preceded the clinical trials; details vary by compound.

Known risks

  • Excellent tolerability.characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Long-term safety in off-label use

Frequently asked questions

References

Systematic references are being expanded; verify sources directly before any decision.