Description
Ipamorelin Peptide for Advanced Growth Hormone Secretagogue and Neuroendocrine Research
Product Overview
Ipamorelin Peptide is a synthetic pentapeptide growth hormone secretagogue specifically engineered to activate the Growth Hormone Secretagogue Receptor Type 1a (GHS-R1a) with high receptor selectivity. Unlike earlier members of the GHRP family, Ipamorelin has been extensively investigated for its selective pharmacological profile, allowing researchers to study growth hormone axis regulation while minimizing activation of other endocrine pathways within experimental models.
Published scientific literature has explored Ipamorelin Peptide in laboratory investigations involving hypothalamic-pituitary communication, pulsatile growth hormone secretion, intracellular receptor signaling, peptide pharmacodynamics, and insulin-like growth factor-1 (IGF-1) regulation. Its defined amino acid sequence, enhanced stability through non-natural amino acid incorporation, and receptor specificity have made it a preferred experimental compound for mechanistic endocrine research.
Researchers also utilize Ipamorelin Peptide to examine G protein-coupled receptor biology, calcium-dependent signaling, cyclic AMP modulation, MAPK activation, and neuroendocrine communication. These studies contribute to a broader understanding of peptide-mediated signaling and endocrine physiology without implying clinical applications.
Each batch is synthesized under rigorous quality-controlled manufacturing procedures, analytically verified for purity and identity, and supplied as a stable lyophilized powder with a comprehensive Certificate of Analysis to support reproducible laboratory research.
For research use only. Not intended for human consumption or clinical use.
Key Research Highlights
- Highly selective synthetic growth hormone secretagogue
- Potent agonist of the Growth Hormone Secretagogue Receptor (GHS-R1a)
- Frequently investigated in pulsatile growth hormone secretion studies
- Evaluated in pituitary and neuroendocrine signaling research
- Studied for IGF-1 pathway regulation in laboratory models
- Utilized in receptor pharmacology and peptide signaling investigations
- Contains non-natural amino acids for enhanced metabolic stability
- High-purity lyophilized formulation suitable for research applications
- Certificate of Analysis (COA) included with every batch
- Manufactured under stringent analytical quality standards
- Excellent batch-to-batch reproducibility
- Suitable for biotechnology, pharmaceutical, and academic laboratories
Why Researchers Choose This Product
- ≥99% research-grade purity verified through analytical testing
- High receptor selectivity for GHS-R1a
- Excellent structural stability and sequence verification
- Reliable reproducibility across laboratory studies
- Comprehensive Certificate of Analysis included
- Stable lyophilized formulation for long-term storage
- Suitable for endocrinology and peptide pharmacology research
- Manufactured using rigorous peptide synthesis protocols
- Available in multiple research quantities
- Intended exclusively for scientific laboratory investigations
Research Applications
Growth Hormone Secretagogue Research
Ipamorelin Peptide is extensively utilized in laboratory investigations examining physiological growth hormone release, endocrine regulation, and pulsatile secretion mechanisms.
GHS-R1a Receptor Pharmacology
Researchers employ Ipamorelin Peptide to investigate receptor binding, G protein activation, ligand selectivity, receptor internalization, and downstream signaling pathways associated with GHS-R1a activation.
Neuroendocrine Biology
Experimental models utilize Ipamorelin Peptide to study hypothalamic-pituitary communication, peptide-mediated endocrine signaling, hormonal feedback regulation, and neuroendocrine physiology.
IGF-1 Signaling Research
Scientists investigate molecular mechanisms linking growth hormone secretagogue receptor activation with insulin-like growth factor-1 production, transcriptional regulation, and downstream signaling networks.
Cellular Signal Transduction
Ipamorelin Peptide is incorporated into studies evaluating phospholipase C activation, intracellular calcium mobilization, MAPK/ERK signaling, PI3K/Akt pathways, and protein kinase-mediated cellular communication.
Peptide Pharmacology
Researchers utilize Ipamorelin Peptide for peptide stability studies, receptor specificity analysis, pharmacokinetic investigations, formulation development, and structure-function relationship research.
Product Specifications
| Specification | Details |
|---|---|
| Product Name | Ipamorelin Peptide |
| Synonyms | Ipamorelin Acetate, GHS Pentapeptide |
| Purity | ≥99% (HPLC Verified) |
| Molecular Formula | C₃₈H₄₉N₉O₅ |
| Molecular Weight | 711.85 g/mol |
| CAS Number | 170851-70-4 |
| Sequence | Aib-His-D-2-Nal-D-Phe-Lys-NH₂ |
| Appearance | White to off-white lyophilized powder |
| Solubility | Soluble in sterile bacteriostatic water and laboratory-grade aqueous buffers |
| Storage Conditions | Store lyophilized peptide at 2–8°C. For long-term storage, maintain at −20°C in a dry, light-protected environment. Avoid repeated freeze-thaw cycles after reconstitution. |
| Available Sizes | 5 mg, 10 mg |
Mechanism of Action
Ipamorelin Peptide is a highly selective synthetic agonist of the Growth Hormone Secretagogue Receptor Type 1a (GHS-R1a), a Class A G protein-coupled receptor expressed predominantly in the anterior pituitary and hypothalamus. Laboratory investigations utilize Ipamorelin to study receptor-mediated endocrine signaling and the molecular regulation of physiological growth hormone secretion.
Following receptor binding, Ipamorelin activates Gq/11 proteins, stimulating phospholipase C (PLC) and promoting the hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP₂) into inositol 1,4,5-trisphosphate (IP₃) and diacylglycerol (DAG). These intracellular second messengers trigger calcium release from the endoplasmic reticulum and activate protein kinase C (PKC), initiating signaling cascades that regulate exocytosis of growth hormone-containing secretory granules within pituitary somatotroph cells.
Published research has demonstrated that GHS-R1a activation by Ipamorelin also influences downstream pathways including MAPK/ERK, PI3K/Akt, and calcium/calmodulin-dependent signaling networks. These pathways regulate transcriptional activity, peptide secretion, receptor trafficking, and cellular adaptation within endocrine tissues. Researchers continue to investigate these molecular mechanisms to better understand receptor pharmacodynamics and neuroendocrine physiology.
Unlike several earlier growth hormone secretagogues, Ipamorelin has been extensively characterized for its high receptor selectivity in experimental systems. Laboratory studies indicate that it produces robust activation of GHS-R1a while exhibiting comparatively limited interaction with signaling pathways associated with other anterior pituitary hormones. This pharmacological profile has made Ipamorelin an important research compound for evaluating isolated GHS-R1a-mediated cellular responses and receptor-specific intracellular signaling.
Additional investigations examine the relationship between GHS-R1a activation and downstream regulation of insulin-like growth factor-1 (IGF-1), endocrine feedback mechanisms, receptor desensitization, peptide metabolism, and hypothalamic-pituitary communication. Owing to its defined pentapeptide sequence, favorable stability profile, and reproducible biochemical activity, Ipamorelin Peptide remains a valuable research reagent in endocrinology, molecular pharmacology, peptide chemistry, cellular signaling, and biotechnology laboratories.
For research use only. Not intended for human consumption or clinical use.





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