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

IpamorelinvsSemax

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

APhase 1Reviewed21/57 cited
BHuman-MechanisticDraft12/39 cited
Ipamorelin
Selective GHRP · Ghrelin Mimetic
200–300 mcgPer doseRaun 1998
Phase 1Evidence levelRaun 1998Sigalos 2018
~2 hrHalf-lifeRaun 1998
SQ · Multiple sites · 1–3×/day
Semax
Cognitive enhancer · Russian Pharma
200–600 mcg/doseIntranasalKaplan 2017
HumanMechanisticKaplan 2017
~30 minOnset
Intranasal · 2–3×/day during cognitive demand

01Mechanism of Action

Parameter
Ipamorelin
Semax
Primary target
Ghrelin receptor (GHS-R1a) on anterior pituitaryRaun 1998
BDNF / NGF expression + monoamine modulationKaplan 2017
Pathway
GHS-R1a binding → Gαq/11 → ↑intracellular Ca²⁺ → GH vesicle exocytosisRaun 1998Bowers 1991
↑ BDNF + NGF synthesis + 5-HT modulation → neuroplasticity + anxiolysis + cognitive enhancementKaplan 2017
Downstream effect
GH pulse amplification, IGF-1 elevation, recovery and lipolytic effectsBowers 2002
Improved memory + attention; reduced anxiety; neuroprotection in ischemiaKaplan 2017
Feedback intact?
Yes — pulsatile pattern preserved; somatostatin feedback activeBowers 2002
Origin
Pentapeptide H-Aib-His-D-2-Nal-D-Phe-Lys-NH₂; rationally designed for ghrelin-receptor selectivityRaun 1998
Synthetic 7-AA peptide derived from ACTH(4-7) with C-terminal Pro-Gly-Pro stabilising tailKaplan 2017
Antibody development
Not reported in short-term studies

02Dosage Protocols

Parameter
Ipamorelin
Semax
Standard dose
200–300 mcg per injectionRaun 1998
Anecdotal community range; clinical doses 1–3 mg IV in trials.
200–600 mcg / dose intranasalKaplan 2017
Frequency
1–3× per day
Once daily pre-sleep is most common; twice or thrice for advanced users.
2–3× per day during cognitive demand
Lower / starter dose
100 mcg per dose
100 mcg / dose
Evidence basis
Phase 1 + clinical practiceRaun 1998Sigalos 2018
Human-mechanistic + Russian clinicalKaplan 2017
Duration
8–12 weeks on / 4 weeks off (anecdotal)
GHS-R desensitisation reported with continuous dosing.
10–14 day cycles, repeated PRN
Reconstitution
Bacteriostatic water; typical 2 mL per 5 mg vial
Pre-formulated nasal spray (commercial); research vial: bacteriostatic water
Timing
Pre-sleep + fasted preferred; 30 min away from food
Morning + early afternoon
Half-life
~2 hoursRaun 1998
Longer than GHRP-6 (15 min); shorter than CJC-1295-DAC (~8 days).
Short plasma; CNS effect lasts ~3–6 hr

04Side Effects & Safety

Parameter
Ipamorelin
Semax
Cortisol elevation
Negligible vs other GHRPsRaun 1998
Prolactin elevation
NegligibleRaun 1998
Hunger
Mild appetite increase via ghrelin-receptor crosstalk
Injection site reaction
Mild irritation possible
GH excess (overdose)
Joint pain, edema, insulin resistance
IGF-1 elevation
Dose-dependent; monitor with chronic high-dose use
Cancer risk
Theoretical via GH/IGF-1 axis; contraindicated in active malignancy
Pregnancy / OB
Avoid
Avoid
Nasal irritation
Mild burning or congestion (transient)
Sleep disruption
Late-day dosing may interfere with sleep
Headache
Uncommon, transient
Long-term safety
Limited Western RCT data
Absolute Contraindications
Ipamorelin
  • ·Active malignancy or cancer history
  • ·Pregnancy / breastfeeding
  • ·Disrupted hypothalamic-pituitary axis
Semax
  • ·Pregnancy / breastfeeding
Relative Contraindications
Ipamorelin
  • ·Untreated diabetes
  • ·Severe insulin resistance
  • ·Concurrent corticosteroid use (theoretical desensitisation)
Semax
  • ·Active psychiatric instability
  • ·Concurrent strong stimulants

05Administration Protocol

Parameter
Ipamorelin
Semax
1. Reconstitution
Add 2 mL bacteriostatic water to 5 mg vial → 2.5 mg/mL. Roll gently. Solution should be clear.
Pre-formulated nasal spray (commercial) or research vial reconstituted with bacteriostatic water.
2. Injection site
Subcutaneous, abdomen or thigh. Rotate sites. Pinch fat for shallow SQ delivery.
Intranasal — 2–3 sprays per nostril per dose. Tilt head slightly back.
3. Timing
Pre-sleep optimal — aligns with natural GH pulse. Some protocols add a morning fasted dose.
Morning + early afternoon. Avoid evening (sleep disruption).
4. Storage
Lyophilised: room temp, protected from light. Reconstituted: refrigerate 2–8 °C, use within 30 days.
Refrigerate after reconstitution; light-protected.
5. Needle
29–31G, 4–8 mm insulin syringe.
Cycle on/off to avoid neurochemical adaptation.

06Stack Synergy

Ipamorelin
+ Tesamorelin
Strong
View Tesamorelin

Ipamorelin (GHRP) + tesamorelin (GHRH analogue) is the textbook dual-axis GH stack. They activate two distinct pituitary receptors — the ghrelin receptor and the GHRH receptor — producing a synergistic GH pulse larger than either alone. Ipamorelin's selectivity (no cortisol/prolactin spike) makes it the ideal GHRP partner for long-term protocols.

Ipamorelin
200–300 mcg SQ · pre-sleep
Tesamorelin
2 mg SQ · same injection · pre-sleep
Primary benefit
Maximal GH pulsatility, fat loss, recovery, sleep depth
+ CJC-1295 (no DAC)
Strong
View CJC-1295 (no DAC)

CJC-1295 (no DAC) is a short-acting GHRH analogue. Combined with ipamorelin (GHRP), the pulse is amplified across both receptor systems with timing similar to native physiology. Without the DAC modification, the stack maintains sharp peaks rather than the sustained elevation seen with CJC-1295-DAC + ipamorelin.

Ipamorelin
200–300 mcg SQ · pre-sleep
CJC-1295 (no DAC)
100 mcg SQ · same injection
Primary benefit
Pulsatile GH stimulation matching physiological pattern
Semax
+ Selank
Moderate
View Selank

Semax (cognitive enhancer, BDNF/NGF) and Selank (anxiolytic + immune) form the canonical Russian "neuro stack" — both intranasal peptide bioregulators with complementary axes. Semax for cognitive demand; Selank for stress mitigation.

Semax
200–600 mcg intranasal · morning + afternoon
Selank
150–300 mcg intranasal · midday + early evening
Primary benefit
Cognitive enhancement + stress mitigation