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CJC-1295 (No DAC) + GHRP-6 (Blend)
CJC-1295 (no DAC) and GHRP-6 work through separate pathways to boost natural growth hormone release, potentially enhancing recovery and appetite.
Quantity: 1
All peptides arrive in powdered form for stability
What is CJC-1295 (No DAC) + GHRP-6 (Blend)?
CJC-1295 without Drug Affinity Complex (no DAC) is a short-acting synthetic analog of growth hormone–releasing hormone (GHRH) that stimulates the pituitary gland to release GH in a pulsatile, physiologic pattern. GHRP-6 (Growth Hormone Releasing Peptide-6) is a hexapeptide growth hormone secretagogue that activates the ghrelin receptor to trigger GH release through a separate pathway. GHRP-6 is also known for stimulating appetite via ghrelin-mimicking effects. When combined, these peptides may amplify GH output and recovery potential by targeting two independent GH stimulation pathways.
Potential Benefits Shown in Studies
Possible benefits of CJC‑1295 (No DAC) + GHRP‑6 Blend
- Amplified GH Release
- Enhanced Muscle Growth & Recovery
- Improved Fat Metabolism
- Natural GH Rhythm Preservation
- Support for Anti‑Aging & Sleep
Mechanisms of Action
CJC-1295 (no DAC) + GHRP-6 may work together by:
- CJC-1295 (no DAC): Activating GHRH receptors for short bursts of natural GH release
- GHRP-6: Triggering ghrelin receptors for additional GH release and appetite stimulation
- Increasing IGF-1 to support muscle repair, connective tissue healing, and collagen synthesis
- Potentially enhancing metabolism and recovery capacity in research settings
- Producing synergistic GH output by combining GHRH and ghrelin receptor activation
CJC-1295 (No DAC) + GHRP-6 (Blend) Research Highlights
Combining CJC‑1295 (No DAC) with GHRP‑6 leverages two independent hormonal pathways, leading to amplified GH release through dual receptor engagement.
Source: muscleandbrawn
Blending a GHRH analog (CJC‑1295 no DAC) with a GHS like GHRP‑6 activates separate receptors to potentiate growth hormone release.
Source: peptidereport
CJC‑1295 (No DAC) mimics natural GH pulses without receptor desensitization risk, thanks to its short half-life.
Source: pep-pedia
