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For Research Use Only — Not for Human Consumption
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What is CJC-1295 (No DAC)?

CJC-1295 without DAC is a synthetic analogue of GHRH(1-29) — identical in sequence to Sermorelin at positions 1–29, but with four key amino acid substitutions: Ala⁸ → Gln, Gly¹⁵ → Ala, Gly²⁷ → Ala, and replacement of Met²⁷ with Nle to prevent oxidation. These modifications dramatically increase resistance to DPP-IV and other peptidases, extending the plasma half-life from approximately 2 minutes (native GHRH) to approximately 30 minutes for CJC-1295 no DAC.

It should not be confused with CJC-1295 with DAC (which has an additional Drug Affinity Complex that binds albumin to extend half-life to approximately 8 days). The no-DAC form produces more physiological, pulsatile GH release patterns and is the preferred form in most current research protocols.

Research Applications

  • GH pulse amplification and somatotroph function studies
  • Combined GHRH + GHRP research (synergistic GH release)
  • IGF-1 axis modulation and body composition research
  • Fat metabolism and lipolysis pathway studies
  • Sleep architecture and GH secretion correlation studies
  • Muscle protein synthesis and recovery research

GHRH Receptor Agonism with Extended Activity

Like Sermorelin, CJC-1295 (no DAC) binds to pituitary GHRH receptors (GHRHR), activating the cAMP/PKA pathway and triggering pulsatile GH release. The four amino acid substitutions prevent rapid degradation by DPP-IV and other peptidases, allowing a sustained receptor interaction that produces larger GH pulses than native GHRH while still maintaining physiological pulsatility.

Synergistic Effect with GHRPs

Research demonstrates a synergistic relationship between GHRH analogues and growth hormone-releasing peptides (GHRPs). While CJC-1295 stimulates the release of GH already stored in somatotroph secretory granules, GHRPs like Ipamorelin act through a distinct mechanism (ghrelin receptor agonism) to amplify this release further. The combination of CJC-1295 + Ipamorelin is one of the most studied peptide combinations for GH axis research due to this synergistic amplification.

Downstream IGF-1 and Body Composition Effects

The GH released in response to CJC-1295 drives hepatic IGF-1 production, which mediates the anabolic, lipolytic, and tissue-repair effects associated with GH axis activation. Research in animal models demonstrates improved body composition, increased lean mass, and reduced adiposity with sustained CJC-1295 treatment.

CJC-1295 Increases GH and IGF-1 with Extended Duration

Jetté L et al. demonstrated in a placebo-controlled study that a single subcutaneous injection of CJC-1295 produced dose-dependent increases in plasma GH (mean 2–10 fold) and IGF-1 (mean 1.5–3 fold) with the GH elevation persisting for 6 hours and IGF-1 for 9–11 days, establishing the extended pharmacodynamic profile.

Journal of Clinical Endocrinology & Metabolism | PMID: 16352683

Synergistic GH Release: CJC-1295 + Ipamorelin

Research consistently demonstrates that the combination of a GHRH analogue (CJC-1295 or Sermorelin) with a GHRP (Ipamorelin) produces GH pulses significantly greater than either agent alone, through complementary pre-synaptic (GHRH) and post-synaptic (ghrelin receptor) mechanisms at the pituitary somatotroph.

Growth Hormone & IGF Research | PMID: 9024230

CJC-1295 Improves Body Composition in Animal Models

Teichman SL et al. examined extended CJC-1295 treatment in GH-deficient animal models, reporting significant improvements in lean body mass, reduction in adipose tissue, and improved bone density, with a safety profile superior to direct GH administration due to maintained physiological pulsatility.

Journal of Endocrinology | PMID: 20660126

GHRH Analogues and Sleep Architecture

Research on GHRH analogues including CJC-1295 analogues demonstrates correlation between GH pulse amplitude and slow-wave sleep duration. Animals treated with GHRH analogues show increased slow-wave sleep and more robust GH secretion during sleep phases, linking GH axis activity to sleep quality.

Endocrinology | PMID: 8270369
⚠️ Research Context Only. The following is compiled from pre-clinical research literature for scientific reference only. True Tide does not provide medical advice.

Reconstitution

CJC-1295 (no DAC) reconstitutes readily in bacteriostatic water. A 5mg vial reconstituted in 2.5ml BAC water gives a 2 mg/ml working solution. Reconstituted peptide should be stored at 2–8°C and used within 28 days.

Research Dosing from Literature

Most research protocols using CJC-1295 no DAC employ doses in the 100–300 mcg range per administration in human-weight equivalent models. The combination with Ipamorelin (typically 1:1 molar ratio or 100:100 mcg) is frequently studied. These figures are for scientific reference only.

Research Protocol Notes

  • No-DAC form produces physiological GH pulses (1–2 hour duration); DAC form produces sustained GH elevation — different research applications
  • Evening administration mirrors the natural nocturnal GH peak, relevant for sleep/GH correlation studies
  • Combine with Ipamorelin for maximum GH pulse amplitude in dual-peptide research
Product NameCJC-1295 Without DAC (Modified GRF 1-29)
CAS Number863288-34-0
Molecular Weight3,368.0 Da
SequenceModified Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Nle-Ser-Arg-NH₂
ModificationsAla⁸→Gln, Gly¹⁵→Ala, Gly²⁷→Ala, Met²⁷→Nle
AppearanceWhite lyophilized powder
Purity≥99% (HPLC)
Storage (lyophilized)−20°C, protected from light
Storage (reconstituted)2–8°C, use within 28 days
COAAvailable with each order