Side-by-side comparison: effects, dosing ranges, side effects, regulatory status, and reconstitution.
Peptide A
Longevity
Synthetic pineal tetrapeptide that activates telomerase and modulates melatonin production.
Peptide B
Longevity
Mitochondrial-derived peptide that mimics exercise and regulates metabolic homeostasis.
Typical vial
10 mg
Typical dose
5000-10000 mcg
Half-life
~30 minutes (short half-life but biological effects persist due to gene expression changes)
FDA status
Not FDA approved for human use. No clinical trials submitted…
Typical vial
5 mg
Typical dose
5000-10000 mcg
Half-life
Not well characterized in humans (estimated hours based on peptide size)
FDA status
Not FDA approved. Investigational compound with no clinical …
Epithalon effects
MOTS-c effects
Epithalon side effects
MOTS-c side effects
Epithalon dosing ranges
Anti-aging and telomere support
5-10 mg · Once daily (SubQ) · 10-20 days, repeated 1-2 times per year
MOTS-c dosing ranges
Metabolic optimization and longevity
5-10 mg · Three to five times weekly (SubQ) · 4-8 weeks
Epithalon: Synthetic pineal tetrapeptide that activates telomerase and modulates melatonin production. Typical dose 5000-10000 mcg. MOTS-c: Mitochondrial-derived peptide that mimics exercise and regulates metabolic homeostasis. Typical dose 5000-10000 mcg. Both fall under the Longevity category.
Stacking Epithalon with MOTS-c is a protocol-design question best raised with a clinician — it depends on your goal, current bloodwork, and whether both peptides target overlapping mechanisms. Both peptides should be tracked independently with separate injection sites and timing. PinnyPeptide supports multi-peptide stacks with automatic injection site rotation.
Epithalon is typically dosed: Once daily (SubQ) for Anti-aging and telomere support. MOTS-c is typically dosed: Three to five times weekly (SubQ) for Metabolic optimization and longevity.
Epithalon: Not FDA approved for human use. No clinical trials submitted to the FDA. MOTS-c: Not FDA approved. Investigational compound with no clinical trials completed for regulatory submission.
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