Ipamorelin

Ipamorelin is a highly selective growth hormone secretagogue pentapeptide that binds the ghrelin receptor without affecting ACTH, prolactin, or cortisol release. It is researched for applications in bone health, muscle preservation, diabetes, and gastrointestinal motility.

Ipamorelin is a short pentapeptide capable of binding to the ghrelin/growth hormone secretagogue receptor. It is one of the most selective growth hormone (GH) secretagogues known, with no measurable effect on ACTH, prolactin, follicle-stimulating hormone, luteinizing hormone, thyroid-stimulating hormone, or cortisol release.

Overview

Ipamorelin was first characterized as a selective GH secretagogue in the late 1990s by Raun et al. (1998), who demonstrated that it stimulates growth hormone release without the broad hormonal side effects seen with other GH secretagogues like GHRP-6 or hexarelin. Its presence plays a key role in the overall growth and repair of musculoskeletal tissue. Despite promising early studies, interest in ipamorelin has waned following the decision not to pursue it as a treatment for post-operative ileus, though it remains a compound of significant research interest.

Mechanism of Action

Ipamorelin acts as a selective agonist of the growth hormone secretagogue receptor (GHS-R1a), also known as the ghrelin receptor. Upon binding, it stimulates pulsatile growth hormone release from the anterior pituitary in a dose-dependent manner. Unlike other GH secretagogues, ipamorelin does not significantly stimulate the release of cortisol or ACTH even at high doses, making it one of the cleanest GHS compounds identified to date.

Reconstitution Calculator

Ipamorelin

**Ipamorelin** is a short pentapeptide capable of binding to the ghrelin/growth

Draw Volume
0.080mL
Syringe Units
8units
Concentration
2,500mcg/mL
Doses / Vial
25doses
Vial Total
5mg
Waste / Vial
0mcg
Syringe Cap.
100units · 1mL
Recommended Schedule
M
T
W
T
F
S
S
Frequency5 on / 2 off
TimingBefore bed
Cycle12-16 weeks
NoteCan dose 2-3x/day for enhanced effect
How to reconstitute
Gather & prepare
1/6Gather & prepare

Set up a clean workspace with all supplies ready.

1.Wash hands thoroughly, put on disposable gloves
2.Your 5mg peptide vial (lyophilized powder)
3.Bacteriostatic water (you'll need 2mL)
4.A 3–5mL syringe with 21–25 gauge needle for reconstitution
5.Alcohol swabs (70% isopropyl)
Use bacteriostatic water (0.9% benzyl alcohol) for multi-dose vials. Sterile water is only safe for single-use.
Supply Planner

5x / week for weeks

80%
1vial
20 doses35 days/vial5 leftover
Cost Breakdown
Vial price
$0.00per dose
$0.00 /week$0 /month
Store 2-8°C30 day shelf lifeSwirl gentlyFor research purposes only

Research

Bone Health

One of the most studied applications of ipamorelin is in counteracting glucocorticoid-induced bone loss. Studies in rats indicate that ipamorelin can completely arrest bone loss caused by corticosteroids and leads to a four-fold increase in bone formation in steroid-treated animals Andersen et al. (2001). Further research demonstrates that ipamorelin increases bone mineral density systemically, strengthening both existing bone and newly formed bone Svensson et al. (2000). As an added benefit, ipamorelin helps offset other steroid side effects such as muscle wasting and increased visceral fat deposition.

Muscle Growth

There is evidence that GH secretagogues like ipamorelin may reduce the catabolic effects of glucocorticoids on muscle. Research in rats given glucocorticoids shows decreased nitrogen wasting in the liver and improved nitrogen balance following ipamorelin administration Aagaard et al. (2009). The ability to counteract both muscle catabolism and bone density loss with a single compound could be particularly beneficial for patients requiring long-term glucocorticoid therapy.

Diabetes

Research in diabetic rats has revealed that ipamorelin can potentiate insulin release, most likely through indirect stimulation of calcium channels on pancreatic islet cells Adeghate & Ponery (2004). This action on the pancreas may help clarify the functional limitations of type 2 diabetes and lead to the development of novel therapeutics or preventative measures.

Post-Operative Ileus

Post-operative ileus (POI) is a common condition following abdominal surgery, characterized by cessation of GI function and inability to tolerate oral nutrition. Ipamorelin has been investigated in several proof-of-concept clinical trials, with results suggesting that it shortens time to first meal by approximately 12 hours Beck et al. (2014), Greenwood-Van Meerveld et al. (2012). Despite early limited success, the trials were discontinued when the sponsoring company determined that efficacy was insufficient for a viable commercial product.

Ghrelin Receptor Probe

The ghrelin receptor increases in abundance in certain cancers and heart failure. Researchers have speculated that ipamorelin could serve as a probe in positron emission tomography (PET) for diagnostic purposes. In vitro studies have demonstrated the feasibility of this approach, confirming that ipamorelin, which is easy to synthesize, could theoretically be used as a PET probe Fowkes et al. (2018).

Safety Profile

Ipamorelin is considered one of the safest GH secretagogues studied to date due to its high selectivity. In clinical trials for post-operative ileus, the most commonly reported side effects were mild and included nausea, headache, and transient flushing. Importantly, ipamorelin does not cause significant changes in cortisol, ACTH, or prolactin levels even at supraphysiological doses, distinguishing it from less selective compounds like GHRP-6 and hexarelin. No serious adverse events have been attributed to ipamorelin in published clinical or preclinical studies.

Pharmacokinetic Profile

Ipamorelin — Pharmacokinetic Curve

Subcutaneous injection
0%25%50%75%100%0m2h4h6h8h10hTimeConcentration (% peak)T_max 42mT_1/2 2h
Half-life: 2hT_max: 40mDuration shown: 10h

Ongoing & Future Research

  • Investigation of ipamorelin-based PET probes for imaging ghrelin receptor expression in cancers and heart failure (DOI: 10.1016/j.ejmech.2018.08.078).
  • Research into ipamorelin for age-related sarcopenia and frailty.
  • Potential applications in osteoporosis prevention during long-term glucocorticoid therapy.
  • Interest in orally bioavailable ghrelin receptor agonist development inspired by ipamorelin's selectivity profile.

Quick Start

Typical Dose
200-300 mcg per injection
Frequency
1-3 times daily depending on goals (1x for longevity, 2-3x for performance)
Route
Subcutaneous injection
Cycle Length
3-6 months
Storage
Lyophilized: Room temperature. Reconstituted: 2-8°C, use within 28 days

Molecular Structure

2D Structure
Ipamorelin molecular structure
Molecular Properties
Formula
C38H49N9O5
Weight
711.85 Da
Length
5 amino acids
CAS
170851-70-4
PubChem CID
9831659
Exact Mass
711.3857 Da
LogP
1.8
TPSA
240 Ų
H-Bond Donors
8
H-Bond Acceptors
8
Rotatable Bonds
19
Complexity
1200
Identifiers (SMILES, InChI)
InChI
InChI=1S/C38H49N9O5/c1-38(2,41)37(52)47-32(21-28-22-42-23-43-28)36(51)46-31(20-25-15-16-26-12-6-7-13-27(26)18-25)35(50)45-30(19-24-10-4-3-5-11-24)34(49)44-29(33(40)48)14-8-9-17-39/h3-7,10-13,15-16,18,22-23,29-32H,8-9,14,17,19-21,39,41H2,1-2H3,(H2,40,48)(H,42,43)(H,44,49)(H,45,50)(H,46,51)(H,47,52)/t29-,30+,31+,32-/m0/s1
InChIKeyNEHWBYHLYZGBNO-BVEPWEIPSA-N

Research Indications

Growth Hormone

Strong Evidence
Natural GH Stimulation

Consistent GH elevation 30-60 minutes post-injection, maintaining natural pulsatile patterns.

Good Evidence
IGF-1 Enhancement

Increases insulin-like growth factor-1 through natural GH pathways.

Good Evidence
Anti-Aging Benefits

Supports cellular regeneration, collagen synthesis, and tissue repair.

Body Composition

Good Evidence
Lean Mass Development

Promotes muscle growth and maintenance through GH-mediated pathways.

Good Evidence
Fat Loss Support

Enhances lipolysis and metabolic rate through natural GH elevation.

Recovery

Good Evidence
Sleep Quality

Improved sleep latency and increased slow-wave sleep duration.

Moderate Evidence
Exercise Recovery

Enhanced recovery markers and reduced soreness after training.

Research Protocols

subcutaneous Injection

Growth hormone secretagogue administered subcutaneously. Inject 30-60 minutes before bedtime on an empty stomach.

GoalDoseFrequency
Loading phase100 mcgOnce daily
Escalation150 mcgOnce daily
Standard dose200 mcgOnce daily
Full dose250 mcgOnce daily
Reconstitution Guide (5mg vial + 3mL BAC water)
  1. Wipe vial tops with alcohol swab
  2. Draw 3.0 mL bacteriostatic water into syringe
  3. Inject slowly down the inside wall of the peptide vial
  4. Gently swirl to dissolve — never shake
  5. Resulting concentration: 1.67 mg/mL
  6. For 100 mcg dose: draw 6 units (0.06 mL)
  7. For 200 mcg dose: draw 12 units (0.12 mL)
  8. For 250 mcg dose: draw 15 units (0.15 mL)
  9. Store reconstituted vial refrigerated at 2-8°C

Interactions

Peptide Interactions

CJC-1295synergistic

Extends GH release for optimal hormone cycles. Popular combination.

BPC-157synergistic

Enhances GH receptor upregulation and effectiveness.

The most popular research combination. Ipamorelin stimulates GH release via ghrelin receptor (GHS-R1a) while CJC-1295 stimulates via GHRH receptor. These act on different receptor systems on somatotroph cells, producing synergistic GH release greater than either alone. See CJC-1295 + Ipamorelin Blend.

Similar GHRH + GHSR synergy concept. Sermorelin (GHRH analogue) stimulates somatotrophs via GHRH-R while ipamorelin acts via GHS-R1a. See Sermorelin + Ipamorelin Blend.

Both are GHS-R1a agonists but with different selectivity profiles. GHRP-2 is less selective (affects cortisol, prolactin) but may produce greater peak GH. Combined in some research protocols. See Mod GRF + Ipamorelin + GHRP-2 Blend.

TB-500compatible

Complementary for recovery and tissue repair.

Sermorelinmonitor

Both stimulate GH; choose one to avoid receptor oversaturation.

Tesamorelinmonitor

Synergistic GH stimulation possible; monitor IGF-1 levels and adjust doses accordingly.

GHRP-2avoid

Redundant GH pathways may cause receptor desensitization.

GHRP-6avoid

Similar mechanism with higher hunger effects; redundant.

What to Expect

What to Expect

Week 1-2

Improved sleep quality and morning energy

Week 2-4

Enhanced exercise recovery and reduced soreness

Week 4-8

Body composition improvements with increased lean mass

Week 8-12

Continued muscle tone, skin quality, and energy improvements

Safety Profile

Common Side Effects

  • Mild hunger increase 20-30 minutes post-injection
  • Slight drowsiness when taken before bed
  • Water retention (mild)
  • Potential receptor desensitization after 3-4 months

Contraindications

  • Pregnancy or breastfeeding
  • Active cancer or history of cancer
  • Severe kidney or liver disease

Discontinue If

  • Signs of receptor desensitization (reduced response after 3-4 months)
  • Unusual joint pain or swelling
  • Persistent numbness or tingling
  • Loss of effectiveness after 3-4 months (cycle off signal)
  • Persistent injection site reactions or unusual swelling
  • Excessive fatigue, unusual hunger, or sleep disturbances
  • Any concerning or unexpected symptoms
  • Consult a healthcare provider with any concerns

Quality Indicators

What to look for

  • White, fine crystalline powder with no clumping
  • Clear solution after BAC water reconstitution
  • Mild hunger response 20-30 minutes post-injection
  • Slight drowsiness at bedtime doses

Caution

  • Minimal or no physiological response after 2 weeks (check source)

Red flags

  • Yellow or discolored powder (suggests degradation)
  • Cloudy solution after reconstitution
  • No response after extended use

Frequently Asked Questions

References (13)

  1. [1]
    Growth Hormone Stimulation Study (2019)
  2. [2]
    Body Composition Clinical Trial (2020)
  3. [3]
    Sleep Quality Research (2021)
  4. [4]
    Athletic Performance Study (2022)
  5. [5]
    Safety and Tolerability Analysis (2023)
  6. [14]
  7. [15]
  8. [16]
  9. [6]
    Raun et al *Eur Eur. J. Endocrinol. (1998)
  10. [7]
    Andersen et al *Growth Horm Growth Horm. IGF Res. (2001)
  11. [8]
    Svensson et al *J J. Endocrinol. (2000)
  12. [10]
    Adeghate & Ponery *Neuro Endocrinol Neuro Endocrinol. Lett. (2004)
  13. [11]
    Beck et al *Int Int. J. Colorectal Dis. (2014)
Updated 2026-03-08Sources: jabronistore-wiki, peptide-wiki-mdx, pep-pedia, pubchem, peptide-wiki-mdx-v2

On this page