Ipamorelin (2mg x 10), CJC-1295 no DAC (2mg x 10)

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Ipamorelin and CJC-1295 no DAC (Mod GRF 1-29) are synthetic research peptides used together in experimental models to investigate growth hormone axis regulation and somatotropic signaling mechanisms. Ipamorelin is a selective pentapeptide growth hormone secretagogue that acts as an agonist of the growth hormone secretagogue receptor (GHS-R1a), activating Gq/PLC and calcium-dependent intracellular signaling involved in GH release while demonstrating minimal interaction with other pituitary hormones in preclinical systems. CJC-1295 no DAC is a stabilized analog of growth hormone–releasing hormone (GHRH 1-29) that selectively activates the GHRH receptor, stimulating adenylate cyclase and cAMP-mediated signaling in pituitary somatotrophs. Preclinical research employs the combined activation of GHS-R1a and GHRH receptors to examine synergistic GH secretion, hypothalamic–pituitary feedback mechanisms, and endocrine receptor pharmacology in controlled laboratory settings.

For research use only. Not for human consumption.

References:
Bowers CY et al., Ann NY Acad Sci, 1998 865:244–249
Frohman LA et al., Endocr Rev, 2001 22(6):606–648
Svensson J et al., J Endocrinol Invest, 1998 21(9):692–699

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CJC-1295 No DAC is a modified peptide compound associated with growth hormone-releasing hormone (GHRH) research. The No DAC version represents a specific formulation studied by scientists interested in peptide structures, stability, and molecular interactions.

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Ipamorelin and CJC-1295 No DAC are synthetic peptide compounds studied in scientific research environments due to their molecular characteristics.

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