CAS 863288-34-0 / 170851-70-4 · Endocrine Research
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⚠ RESEARCH USE ONLY
This product is sold strictly for in vitro laboratory research use only. Not for human or animal consumption, diagnostic use, or therapeutic application. Purchasers must be qualified researchers or authorized purchasers for a research institution.
The CJC-1295 + Ipamorelin blend combines two synthetic peptides frequently paired in growth-hormone axis research. CJC-1295 is a modified 30-amino-acid growth-hormone-releasing hormone (GHRH) analog engineered for extended half-life. Ipamorelin is a five-amino-acid pentapeptide that acts as a selective growth-hormone secretagogue receptor (GHS-R) agonist. When studied together, the two act on complementary pathways of the somatotropic axis.
In research settings, the blend is examined for pulsatile growth-hormone release, IGF-1 signaling, and pathway crosstalk between GHRH and ghrelin-receptor activation.
Reference: Teichman S. L. et al. (2006), Journal of Clinical Endocrinology & Metabolism, 91(3), 799-805.
CJC-1295 was developed in the mid-2000s by ConjuChem as a long-acting GHRH analog, using a drug-affinity-complex technology that binds to serum albumin to extend circulating half-life beyond native GHRH. Ipamorelin was first described by Novo Nordisk researchers in 1998 as a selective ghrelin-receptor agonist that stimulates growth-hormone release without significant activation of adrenocorticotropic or prolactin pathways. Research pairing the two emerged from interest in dual activation of GHRH and ghrelin receptor pathways as a tool for studying pulsatile hormone release.
Reference: Raun K. et al. (1998), European Journal of Endocrinology, 139(5), 552-561.
CAS #: 863288-34-0
Molecular Formula: C152H252N44O42
Molecular Weight: 3,367.9 g/mol
PubChem CID: 56841945
CAS #: 170851-70-4
Molecular Formula: C38H49N9O5
Molecular Weight: 711.85 g/mol
PubChem CID: 9831659
CJC-1295 and ipamorelin have been examined across pituitary, hepatic, and metabolic research models, both individually and in combination. Reported findings describe pulsatile growth-hormone release patterns, extended IGF-1 elevation with the DAC-modified CJC-1295, and the selective GH-releasing profile of ipamorelin without cortisol or prolactin interference observed with earlier secretagogues.
Key Areas of Research:
Together, these observations make the CJC-1295 + Ipamorelin blend a widely-used research tool for studying dual-pathway activation of the growth-hormone axis in preclinical models.
References: Ionescu M. & Frohman L. A. (2006), Journal of Clinical Endocrinology & Metabolism, 91(12), 4792-4797; Sinha D. K. et al. (2020), Translational Andrology and Urology, 9(Suppl 2), S149-S159.
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