Research Comparison

CJC-1295 (No DAC) vs GHRP-6

CJC-1295 (No DAC) (GHRH analog (short-acting modified GHRH(1-29), aka Mod GRF 1-29)) and GHRP-6 (Growth-hormone secretagogue (GHRP) / ghrelin receptor agonist) are documented as co-studied in the PeptiDex library. This page puts the two entries side by side on class, molecular weight, half-life, origin, mechanism and studied research areas — every value taken from the entry it belongs to.

For research and educational purposes only. This page places two documented library entries next to each other. It is not medical advice, it does not rank one compound above the other or claim either is more effective, and it is not a usage, dosing, or combination recommendation.

Why these two are co-studied

Cross-referenced for research context — not a usage or combination recommendation.

From the GHRP-6 entryShort-acting GHRH analog co-studied with GHRP-6 to model pulsatile combined GH release.
From the CJC-1295 (No DAC) entryGhrelin-receptor GHRP paired with the short-acting GHRH analog for synergistic GH pulses.

At a glance

Side-by-side reference for CJC-1295 (No DAC) and GHRP-6 on compound class, research category, length, molecular weight, half-life and origin.
AttributeCJC-1295 (No DAC)GHRP-6
Compound classGHRH analog (short-acting modified GHRH(1-29), aka Mod GRF 1-29)Growth-hormone secretagogue (GHRP) / ghrelin receptor agonist
Research categoryGrowth & GH-AxisGrowth & GH-Axis
Length (amino acids)29 amino acids6 amino acids
Molecular weightApproximately 3368 g/mol873.0 g/mol
Half-lifeShort, on the order of tens of minutes (reported approximately 30 minutes), longer than native GHRH but far shorter than the DAC versionShort, on the order of tens of minutes (reported approximately 15-60 minutes)
OriginCJC-1295 without DAC (commonly called Mod GRF 1-29 or Modified GRF 1-29) is a modified GHRH(1-29) analog carrying stabilizing amino-acid substitutions but lacking the albumin-binding Drug Affinity Complex (DAC) of the full CJC-1295.GHRP-6 is one of the earliest synthetic hexapeptide growth-hormone secretagogues, developed in the 1980s and instrumental in the discovery of the growth-hormone secretagogue receptor and its endogenous ligand ghrelin.

“Not documented” means the PeptiDex entry records no value for that field. Nothing on this page is estimated, and no figure is carried over from one compound to the other.

How CJC-1295 (No DAC) works

This peptide is a GHRH-receptor agonist that stimulates pulsatile GH release from the pituitary. Its four amino-acid substitutions on the GHRH(1-29) backbone (e.g. at positions 2, 8, 15, 27) resist DPP-4 degradation, giving it a modestly longer half-life than native sermorelin. Without the DAC group, it does not bind albumin, so it produces short, discrete GH pulses rather than sustained elevation.

How GHRP-6 works

GHRP-6 is an agonist of the growth-hormone secretagogue receptor (GHS-R1a, ghrelin receptor), stimulating pulsatile GH release from the pituitary. It is a strong stimulator of appetite via ghrelin-receptor signaling. It can also increase ACTH, cortisol, and prolactin secretion.

Mechanistic descriptions reflect published research-literature understanding and are quoted from each compound's own entry. Much peptide research is preclinical (in-vitro or animal-model); mechanism in humans may differ and is not established for many compounds.

Where each one appears in the literature

The research contexts each entry documents. Listing a research area is not a claim of efficacy or a therapeutic indication, and the two lists are not scored against each other.

CJC-1295 (No DAC)

Pulsatile GH/IGF-1 axis stimulation researchComparative pharmacokinetics of DAC vs no-DAC GHRH analogsStudies combining GHRH analogs with GHRPs for synergistic pulsesBody-composition research (preclinical)

GHRP-6

Historical role in discovery of the GHS receptor and ghrelinResearch on GH secretion and the GH/IGF-1 axisMarked appetite-stimulation research via the ghrelin pathwayStudies on cytoprotective/tissue-repair effects (preclinical)Neuroendocrine (ACTH/cortisol/prolactin) effect studies

What sets each apart

CJC-1295 (No DAC)

The absence of the DAC albumin-binding group makes this a short-acting, pulse-generating GHRH analog, in direct contrast to the long-acting DAC version of CJC-1295.

GHRP-6

GHRP-6 is historically foundational and produces the strongest appetite stimulation among common GHRPs, but is less selective (more cortisol/prolactin) than ipamorelin.

Frequently asked questions

What is CJC-1295 without DAC?

CJC-1295 without DAC (essentially Modified GRF 1-29) is a synthetic 29-amino-acid GHRH analog with four substitutions (at positions 2, 8, 15, and 27) that resist DPP-IV cleavage. Unlike the DAC version, it lacks the albumin-binding complex, so it is short-acting.

How does the no-DAC version differ from CJC-1295 with DAC?

Both share the same modified GHRH(1-29) core, but the no-DAC form has a half-life of only about 30 minutes and produces discrete GH pulses, whereas the DAC form binds albumin and lasts 6-8 days, giving sustained GHRH tone. The choice shapes whether research models pulsatile or sustained GH output.

Is CJC-1295 no-DAC the same as Modified GRF (1-29)?

Effectively yes. CJC-1295 without DAC and Modified GRF (1-29) refer to the same tetra-substituted GHRH(1-29) peptide; the naming differs by supplier but the sequence and short-acting profile are the same.

What is GHRP-6?

GHRP-6 is a synthetic hexapeptide growth hormone-releasing peptide and one of the earliest developed ghrelin-receptor (GHS-R1a) agonists. It stimulates pulsatile GH secretion from the anterior pituitary and served as a foundational research tool for characterizing the GHS-R pathway.

How does GHRP-6 differ from GHRP-2 and hexarelin?

All three share a related hexapeptide scaffold and act on the ghrelin receptor, but GHRP-6 is the least potent and produces the most pronounced appetite stimulation. GHRP-2 is more potent with more cortisol/prolactin effect, and hexarelin is the most potent of the group.

Is GHRP-6 known for stimulating appetite?

Yes. GHRP-6 is the GHRP most strongly associated with hunger in the research literature, reflecting robust ghrelin-receptor agonism. This property makes it of interest in appetite- and feeding-related research models.

Answers are the ones published on each compound's own PeptiDex entry. They are educational summaries of research-literature context and are not medical advice.

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