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- Molecular Formula: C₁₅₂H₂₅₂N₄₄O₄₂
- Molecular Weight: 3367.95 g/mol
- Sequence: H-Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-NH₂
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- Molecular Formula: C₄₅H₅₅N₉O₆
- Molecular Weight: 817.97 g/mol
- Sequence: H-D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH₂
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- Enzymatic Resistance & cAMP Pathways: Modified GRF 1-29 features four precise amino acid substitutions (at the 2nd, 8th, 15th, and 27th positions) designed to resist enzymatic breakdown by dipeptidyl peptidase-4 (DPP-4) and prevent methionine oxidation. Upon binding to pituitary GHRH receptors, it upregulates the adenylyl cyclase pathway, converting ATP to cAMP. This activates protein kinase A (PKA) to open voltage-dependent calcium channels, driving calcium influx and prompting pulsatile growth hormone discharge.
- Phospholipase C Co-Activation & Synergy: GHRP-2 acts downstream via a separate, highly responsive pathway by binding to hypothalamic and pituitary ghrelin receptors (GHS-R1a). This conformational change triggers the phospholipase C (PLC) cascade, splitting cellular substrates into IP3 and DAG. IP3 mobilizes calcium from intracellular stores, compounding the calcium signals initiated by Mod GRF 1-29. This dual-pathway mechanism is heavily researched for its capacity to bypass Somatostatin feedback limits and maximize cellular secretion peaks.
- Pancreatic Islet Survival & Glycemic Regulation: GHRH analogs are actively investigated for their protective role in metabolic models. Preclinical data indicates that short-term exposure can upregulate localized Insulin-Like Growth Factors, improving the cellular proliferation and survival rates of pancreatic islets under diabetic stress. Research models also point to a significant expansion of islet size, increased insulin expression, and a reduction in circulating triglyceride-rich lipoproteins.
- Cardioprotection & Extracellular Matrix Repair: In ischemic and reperfusion models, GHRH agonists have demonstrated notable therapeutic potential. Studies reveal that exposure can optimize end-diastolic pressure, improve stroke work, and limit localized tissue scarring following myocardial injury. This cytoprotection is closely linked to downstream growth hormone cascades that downregulate oxidative stress, promote fibroblast proliferation, and accelerate collagen synthesis required for vascular and skeletal bone mineral density maintenance.
- Verified Purity: ≥ 99% purity guaranteed through mass spectrometry and HPLC profiling.
- USA Vetted: Independent laboratory testing ensures correct molecular weight fractions and zero chemical cross-contaminants.
- Research Use Only: This compound is synthesized exclusively for in vitro laboratory experimentation and preclinical evaluation. Make sure to double-check the physical label to confirm this information.




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