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Specimen Atlas of Research Peptides30 plates · MIT
Side-by-side · Research reference

EpitalonvsMK-677

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

AHuman-MechanisticDraft8/37 cited
BPhase 2Reviewed13/45 cited
Epitalon
Pineal bioregulator · Telomerase activator
5–10 mgPer cycle doseKhavinson 2003
HumanMechanisticKhavinson 2003
HoursHalf-life (est)
SQ or IM · Abdomen · Daily for 10–20 days
MK-677
Oral GHS · Ibutamoren
10–25 mgDaily dose (oral)Nass 2008
Phase 2Evidence levelMurphy 1998Nass 2008
~24 hrHalf-lifeNass 2008
Oral capsule · 1×/day

01Mechanism of Action

Parameter
Epitalon
MK-677
Primary target
Telomerase activity (proposed); pineal melatonin axis modulationKhavinson 2003
Ghrelin receptor (GHS-R1a)Murphy 1998
Pathway
Activation of telomerase reverse transcriptase (hTERT) in somatic cells; pineal-axis modulation supports endogenous melatoninKhavinson 2003
GHS-R1a → Gαq → Ca²⁺ → sustained GH pulses across 24 hrNass 2008
Downstream effect
Telomere elongation, improved sleep architecture, reported lifespan extension in aged miceKhavinson 2003
Sustained GH + IGF-1 elevation; appetite stimulation; lean mass preservationNass 2008
Feedback intact?
Pulsatile pattern preserved despite long half-lifeMurphy 1998
Origin
Synthetic 4-AA peptide derived from epithalamin (a natural pineal extract)Khavinson 2003
Non-peptide spiroindane-piperidine small molecule designed at MerckMurphy 1998
Antibody development

02Dosage Protocols

Parameter
Epitalon
MK-677
Standard dose
5–10 mg / day for 10–20 days, 1–2× per yearKhavinson 2003
Anecdotal community protocol. Russian clinical literature uses similar cycling.
10–25 mg / day oralNass 2008
25 mg used in Nass 2008 elderly trial; 10–15 mg common community dose.
Frequency
Once daily during a cycle
Once daily, oral
Lower / starter dose
2.5 mg / day
5 mg / day
Evidence basis
In-vitro telomerase + Russian clinical trialsKhavinson 2003
Phase 2 trials (Nass 2008, Murphy 1998)Nass 2008Murphy 1998
Duration
10–20 day cycles, 1–2× per year
8–16 weeks per cycle (off-cycle to reset receptor sensitivity)
Reconstitution
Bacteriostatic water
Oral, no reconstitution
Timing
Pre-sleep preferred (pineal alignment)
Pre-sleep preferred for natural GH pulse alignment
Half-life
Hours (estimated)
~24 hrNass 2008
Once-daily dosing covers 24 hours.

04Side Effects & Safety

Parameter
Epitalon
MK-677
Injection site reaction
Mild irritation
Sleep architecture
Improved subjective sleep quality (anecdotal)
Cancer risk
Theoretical via telomerase activation in pre-malignant cells
Contraindicated in active malignancy (GH/IGF-1 axis)
Long-term safety
Limited Western RCT data
Pregnancy / OB
Avoid
Avoid
Antibody formation
Not reported
Increased appetite
Strong appetite increase via ghrelin agonism
Water retention
Mild edema, paresthesias
Glucose tolerance
↑ HbA1c +0.3–0.5% in 2-yr elderly trialNass 2008
IGF-1 elevation
+50–100% sustainedNass 2008
Cardiovascular
No clear adverse signal in trials; congestive heart failure caution
Drowsiness
Common, especially during initial weeks
Absolute Contraindications
Epitalon
  • ·Pregnancy / breastfeeding
  • ·Active malignancy or pre-malignant state
MK-677
  • ·Active malignancy
  • ·Pregnancy / breastfeeding
  • ·Disrupted hypothalamic-pituitary axis
  • ·Congestive heart failure (caution)
Relative Contraindications
Epitalon
  • ·Family history of cancer
MK-677
  • ·Untreated diabetes
  • ·Pre-diabetes
  • ·Severe insulin resistance

05Administration Protocol

Parameter
Epitalon
MK-677
1. Reconstitution
Add 1–2 mL bacteriostatic water to 10 mg vial → 5–10 mg/mL.
Capsule or oral solution. No injection.
2. Injection site
SQ — abdomen preferred. Rotate sites.
Oral. Take with or without food.
3. Timing
Pre-sleep preferred to align with pineal axis.
Pre-sleep preferred — aligns with natural GH pulse.
4. Storage
Lyophilised: room temp, light-protected. Reconstituted: refrigerate ≤30 days.
Capsule: room temp ≤25 °C, dry place.
5. Needle
29–31G, 4–8 mm insulin syringe.
Monitor HbA1c every 8–12 weeks during chronic use.