Rankings / Longevity — Peptides
Humanin
Longevity · Mitochondrial-derived peptide
Tier C+
Bottom line
Read Off Label grades Humanin as C+ (5.3/10) based on preclinical evidence, unknown / varies benefit magnitude, and a low-risk safety profile.
Declines ~60-70% from age 20 to 80 in humans.
Studied, labeled, or reported-use context: No standard clinical dose; usually studied 0. — Research chemical; not individualized guidance.
What the evidence says
Declines ~60-70% from age 20 to 80 in humans. Elevated in centenarians and their offspring. Preclinical: neuroprotective in Alzheimer's models. No human RCTs with hard endpoints — mostly observational biomarker work.
Mechanism
24-amino acid peptide from 16S rRNA; cytoprotective — blocks Bax-induced apoptosis; associated with insulin sensitivity and IGF-1 signaling; declines with age
Studied, labeled, or reported dose & route
No standard clinical dose; usually studied 0.5-2 mg/day in research
This records doses and routes described in studies, approved labeling, clinical practice, or documented use. It is not individualized guidance and does not establish safety; context changes with indication, formulation, health history, monitoring, and other medicines.
Citations
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Common questions
- What does the evidence show about Humanin's effects?
- Read Off Label rates the evidence for Humanin as Preclinical and the benefit magnitude as unknown / varies, producing an overall grade of C+ (5.3/10). Declines ~60-70% from age 20 to 80 in humans.
- What safety findings are reported for Humanin?
- Humanin has a low risk profile in the database. Low (limited safety data) Legal status: Research chemical.
- What doses or routes are reported for Humanin?
- No standard clinical dose; usually studied 0.5-2 mg/day in research This is context from studies, approved labeling, clinical practice, or documented use; it is not individualized guidance and does not establish safety.
- How does Humanin work?
- 24-amino acid peptide from 16S rRNA; cytoprotective — blocks Bax-induced apoptosis; associated with insulin sensitivity and IGF-1 signaling; declines with age
This is an independent synthesis of published research by a non-clinician. Scores are opinions supported by citations, not prescriptions. See the full disclaimer and methodology for how this score was produced and what it does and doesn't mean.