CJC-1295 (without DAC) vs GHRP-6

CJC-1295 (without DAC)

CJC-1295 without DAC, also called modified GRF (1-29), is a 29-residue synthetic analogue of growth hormone-releasing hormone (GHRH). Native GHRH has 44 residues, but its first 29 carry the receptor-binding activity, and this peptide is built on that shortened sequence with four amino-acid substitutions intended to slow breakdown. The name causes confusion: CJC-1295 originally referred to a version carrying a drug affinity complex (DAC), a reactive linker that binds albumin and greatly prolongs circulation. The form described here lacks that linker. Human studies of the DAC version exist but are few; published work on the form without DAC is thinner still, and much of what is said about it is inferred from the parent hormone.

GHRP-6

GHRP-6 is a synthetic hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2, and one of the earliest growth hormone-releasing peptides to be described. It came out of structure-activity work on small synthetic peptides, carried out before anyone knew which receptor they acted on. That receptor, GHS-R1a, was later shown to respond to ghrelin, a hormone made mainly in the stomach, so GHRP-6 is now classed as a ghrelin receptor agonist. It has been used in pituitary cell and receptor assays, in a large body of animal work, and in human endocrine studies of hormone secretion. Because the same receptor takes part in the control of feeding, it has also served as a tool in appetite research.

How CJC-1295 (without DAC) acts

Like native GHRH, the peptide has been reported to bind the GHRH receptor, a class B G protein-coupled receptor on somatotroph cells of the anterior pituitary. Receptor activation couples to Gs, raising intracellular cAMP and releasing stored growth hormone; circulating growth hormone in turn drives IGF-1 production, mainly in the liver. The substitutions, D-alanine at position 2, glutamine at 8, alanine at 15 and leucine at 27, were chosen to resist cleavage by dipeptidyl peptidase-4 and to reduce deamidation and oxidation at vulnerable residues. Without the albumin-binding linker its half-life is short, and pharmacokinetic data specific to this form are sparse.

How GHRP-6 acts

GHRP-6 is reported to bind and activate GHS-R1a, a G protein-coupled receptor that signals mainly through Gq, phospholipase C and intracellular calcium. On pituitary somatotrophs this signalling triggers growth hormone release. The receptor is also expressed in the hypothalamus, including on neuropeptide Y and agouti-related peptide neurons of the arcuate nucleus, which rodent studies have linked to the control of food intake; that distribution is the basis for the peptide's use in feeding research. Small increases in ACTH, cortisol and prolactin have been reported with it in addition to growth hormone. Interactions with somatostatin signalling have been proposed but are less clearly defined.

The records side by side

• Type: CJC-1295 (without DAC), GHRH analog (Modified GRF 1-29); GHRP-6, Growth hormone secretagogue (GHRP)
• Length: CJC-1295 (without DAC), not recorded; GHRP-6, 6 amino acids
• Molecular weight: CJC-1295 (without DAC), 3647.2 g/mol; GHRP-6, 873.0 g/mol
• Molecular formula: CJC-1295 (without DAC), C165H269N47O46; GHRP-6, C46H56N12O6

Reading a comparison

A comparison places two records side by side; it does not merge them. Each description above is drawn from that compound's own record, and the two were not necessarily characterised by the same methods, at the same time, or to the same level of detail. Before comparing any attribute, it is worth establishing that both records describe the substance you think they describe — names are not identifiers, and two entries sharing a name can differ in salt form, stereochemistry or the convention used to state a mass. Where a figure carries no method beside it, the comparison is between two reported numbers rather than between two measurements.