Ipamorelin 50mg Monthly subscription

Original price was: $130.00.Current price is: $100.00. / month

Compound: cetate 

Concentration: 5mg per vial 

Format: Lyophilized White Powder (Strictly for In-Vitro Laboratory Use) 

Chemical Classification: Selective Growth Hormone Secretagogue (GHS)

Chemical Profile: Ipamorelin is a synthetic pentapeptide designed to function as a highly specific agonist of the ghrelin/growth hormone secretagogue receptor (GHS-R1a). It is distinguished by its selectivity; unlike earlier GHRP generations, Ipamorelin stimulates the release of growth hormone (GH) from the anterior pituitary without significantly impacting ACTH, prolactin, follicle-stimulating hormone (FSH), luteinizing hormone (LH), or cortisol levels. This high specificity makes it a critical model peptide for understanding how receptor binding selectivity is achieved and for isolating GH pathways in metabolic research.

Research

  1. Corticosteroid Mitigation & Bone Density Models Glucocorticoids are potent anti-inflammatory agents often limited by catabolic side effects, particularly bone density loss. Preclinical studies in rodent models have utilized Ipamorelin to investigate the reversal of these effects. Research indicates that Ipamorelin administration in rats exposed to corticosteroids resulted in a four-fold increase in bone formation rates and effectively counteracted drug-induced bone loss. Further data suggests a systemic increase in bone mineral density (BMD), highlighting Ipamorelin’s potential role in osteoblast activity and skeletal remodeling mechanisms.
  2. Nitrogen Balance & Muscle Preservation Research focuses on the interaction between Growth Hormone Secretagogues (GHS) and catabolic states. In studies involving glucocorticoid-induced muscle wasting, subjects administered Ipamorelin demonstrated improved nitrogen balance in the liver and a reduction in muscle catabolism. This suggests a pathway by which selective GH stimulation may counteract protein degradation, a primary area of interest for research into cachexia and atrophy models.
  3. Insulin Secretion & Pancreatic Function In diabetic rat models, Ipamorelin has been observed to potentiate insulin release. The proposed mechanism involves the indirect stimulation of calcium channels on pancreatic islet cells, where insulin is synthesized and stored. This interaction provides a window into the functional dynamics of Type 2 diabetes models and the potential for peptide-based modulation of beta-cell function.
  4. Gastric Motility & Post-Operative Ileus (POI) Ipamorelin mimics ghrelin’s effects on the gastrointestinal system, specifically regarding motility. While historical proof-of-concept trials explored its efficacy in reducing Post-Operative Ileus (POI) in clinical settings, current research focuses on the mechanism by which it shortens “time to first meal” and accelerates gastric emptying. It remains a compound of interest for studying synergistic therapies to restore GI function following abdominal trauma.
  5. Diagnostic Imaging (PET Probe) Due to its strong binding affinity for the ghrelin receptor, which is often overexpressed in specific carcinoma tissues and heart failure models, Ipamorelin is being investigated as a potential probe for Positron Emission Tomography (PET). In vitro feasibility studies suggest that radiolabeled Ipamorelin could serve as a diagnostic tool for mapping ghrelin receptor density in vivo.

Disclaimer: This product is sold explicitly as a chemical reagent for laboratory research and testing purposes only. It is not intended for human consumption, diagnostic, or therapeutic use. Bodily introduction of any kind into humans or animals is strictly forbidden by law.

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