Evidence Codex is an educational reference, not medical advice. Many compounds listed are unapproved or have limited human evidence. Read the medical disclaimer.
Energy & Endurance
Limited / unverified Limited / unverified Limited / unverified Mitochondrial Neuroprotective
Educational reference only. Read the full disclaimer. The protocols below are not automatically an FDA-approved or clinically verified regimen unless explicitly marked as label-verified or clinical-trial above.

Overview

Route(s): Subcutaneous

Typical vial sizes: 10 mg

Dosing window: Anytime

Receptor / target: Mitochondrial Receptors

Properties: Not stated

Pre-mixed: No

Unverified protocol notes

Standard Protocol

TimeframeDoseNotes
Weeks 1-62mg - 5mg twice weeklyUnder-researched compared to MOTS-c; dose conservatively.

Unverified protocol note; not label dosing unless graded otherwise on this page.

Protocol logic check

Protocol context: Energy protocols are usually about mitochondrial or metabolic signaling. The logic is timing around meals/training, avoiding late-day stimulation, and watching sleep, glucose, blood pressure, and overtraining signals. Entry context: target (Mitochondrial Receptors); route Subcutaneous; timing Anytime. Limited-evidence dosing tables are hypotheses, not recommendations.

Independent evidence

Independent safety notes: No independent approved-label regimen is listed for this entry. Dosing notes remain unverified.

Regulatory status: no approved label identified

Storage

No independently verified storage guidance found. Treat any unverified storage claim as unverified, and see the general storage guidance in the FAQ.

Contraindications (limited evidence)

  • Active malignancy: Humanin's potent anti-apoptotic mechanisms (Bcl-2 upregulation, Bax inhibition, cytochrome c suppression) that protect healthy cells from death are mechanistically identical to the pathways cancer cells exploit to become chemotherapy-resistant; exogenous Humanin may protect tumor cells from apoptosis-inducing therapy. Limited / unverified
  • Concurrent cytotoxic chemotherapy: Humanin's anti-apoptotic activity directly opposes the mechanism of action of most chemotherapy agents, which rely on triggering apoptosis in rapidly dividing cells. Limited / unverified
  • Known hypersensitivity to Humanin or peptide excipients. Limited / unverified
  • Pregnancy: mitochondrial-encoded peptide signaling in fetal development is not characterized; safety not established. Limited / unverified
  • Breastfeeding: no data. Limited / unverified
  • Pediatric use: no safety data. Limited / unverified
  • Severe cardiac arrhythmia: IGF-1 receptor and STAT3 pathway activation by Humanin may affect cardiac electrophysiology at high doses; limited human data. Limited / unverified

Side effects (limited evidence)

  • Injection site reactions: redness, soreness, mild swelling at subcutaneous injection site; standard peptide injection response; expected and manageable. Limited / unverified
  • Under-documented adverse effects: Humanin has the least human safety data of any compound in Category IV; all side effect characterization derives from animal studies and early-stage human observation; unknown adverse effects may exist that have not yet been documented. Limited / unverified
  • Theoretical protection of cancer cells from apoptosis: the mechanistically most significant theoretical adverse effect; Bcl-2 upregulation and Bax inhibition are the same pathways that confer chemotherapy resistance in cancer; not observed as a clinical adverse event but represents the primary safety concern. Limited / unverified
  • Mild fatigue: reported anecdotally in early weeks of use; possibly related to mitochondrial membrane signaling adjustments. Limited / unverified
  • Mild headache: uncommon; not well characterized. Limited / unverified
  • Potential IGF-1 receptor pathway modulation: Humanin signals through the IGF-1 receptor at certain concentrations; theoretical implications for insulin-sensitive conditions warrant monitoring in diabetic subjects. Limited / unverified
  • No documented endocrine disruption, receptor desensitization, or hormonal suppression in available preclinical literature. Limited / unverified

Compatibility

The relationships below come from the source site's internal engine and were not verified independently. Treat them as a starting point for a conversation with a clinician. They carry no safety guarantee.

Reported synergistic:

Reported contraindicated combinations:

None listed.

Sources