CJC-1295 (no-DAC) — Compound Reference

Compound Reference Log · Deep Dive

CJC-1295 (no-DAC)

The stabilized GHRH(1-29) peptide known as Modified GRF 1-29 — the same backbone as CJC-1295 but without the albumin-binding complex, so it is short-acting.

Mod GRF 1-29GHRH(1-29) analogNo DAC / short-actingResearch use only
Narrated · press play
01

What the name means

“No-DAC” simply signals what is absent: this version lacks the Drug-Affinity-Complex, the albumin-binding group found on the other CJC-1295 form.

Because of that, it is more often called Mod GRF 1-29 — Modified Growth-Hormone-Releasing Factor, residues 1 through 29. GRF (growth-hormone-releasing factor) is an older name for GHRH (growth-hormone-releasing hormone), the hypothalamic signal that triggers growth-hormone release. So the name describes a modified 29-amino-acid piece of GHRH.

02

What it actually is

It is a 29-amino-acid synthetic peptide: the first 29 residues of GHRH carrying four stabilizing substitutions.

Length: 29 amino acids

Bonds: no disulfide bonds; a single linear chain

Type: linear peptide (tetrasubstituted GHRH 1-29)

Origin: fully synthetic; derived from human GHRH

The four changes, relative to the natural GHRH(1-29) sequence, are a D-alanine at position 2, glutamine at position 8, alanine at position 15, and leucine at position 27. These are the same substitutions used in the DAC form; the only difference is that this version has no albumin-binding group attached, so it does not gain the extended circulating life.

03

Where it came from

It is a stabilized derivative of native GHRH, whose active 1-29 fragment underlies both this peptide and Sermorelin.

Human GHRH was characterized in 1982, and its first 29 amino acids were found to retain full biological activity — the same fragment marketed decades ago as Sermorelin. The tetrasubstituted version arose from medicinal-chemistry efforts to make that fragment more chemically robust, and it later served as the peptide backbone onto which the DAC group was added to create long-acting CJC-1295.

04

Why it was created — the thought process

The substitutions were introduced to fix specific chemical weak points in the natural sequence.

Native GHRH is rapidly clipped by the enzyme DPP-IV at its second residue and is vulnerable to oxidation and rearrangement at other positions. Replacing those residues — a protected D-alanine at position 2, and swaps at positions 8, 15 and 27 — makes the peptide meaningfully more stable than plain Sermorelin. Even so, without the albumin-binding DAC group, its half-life in circulation is still on the order of minutes, which is the defining practical difference between this form and the DAC form.

05

How it is made

It is manufactured by solid-phase peptide synthesis.

The 29-residue chain is built stepwise on a resin (SPPS), cleaved, purified by high-performance liquid chromatography, and verified by mass spectrometry. Because there is no conjugation step, the process is simpler than for the DAC form; quality control centers on sequence fidelity and purity.

06

What the research actually shows — honestly

This is an important honesty point: the published human data on “CJC-1295” describe the DAC form, not this one.

Modified GRF 1-29 has been studied in preclinical settings as a growth-hormone-releasing peptide, but it does not have its own dedicated human clinical trials establishing benefit or safety. Discussions that cite human growth-hormone or IGF-1 responses to “CJC-1295” are generally referring to the long-acting DAC version, which behaves very differently in the body. Treating the two as interchangeable is a common and misleading error.

This material is offered only as a research and educational reference. It is not a drug or supplement, and no dosing, timing, or usage information is provided or implied.

07

Selected research & sources

The items below are drawn from the peer-reviewed literature (PubMed) and describe results observed in research models or reported in the clinical literature. They are listed so the evidence can be examined at its source — not to suggest any use.

  1. Teichman SL, et al. J Clin Endocrinol Metab. 2005. “Prolonged stimulation of GH and IGF-I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults.” doi.org/10.1210/jc.2005-1536
  2. Memdouh S, et al. Drug Test Anal. 2021. “Advances in the detection of growth hormone releasing hormone synthetic analogs.” doi.org/10.1002/dta.3183
  3. Coppieters G, et al. J Pharm Biomed Anal. 2022. “An antibody-free, ultrafiltration-based assay for GHRH analogues in urine.” doi.org/10.1016/j.jpba.2022.114726
  4. Timms M, et al. Drug Test Anal. 2018. “An immuno-PCR screen for CJC-1295 and other GHRH analogs in equine plasma.” doi.org/10.1002/dta.2554
  5. Pont L, et al. J Chromatogr A. 2020. “Immunopurification of growth hormone-releasing hormones prior to LC-HRMS.” doi.org/10.1016/j.chroma.2020.461548

Regulatory status: Not FDA-approved for any indication. Prohibited by the World Anti-Doping Agency.

◆ A reference, not a recommendation

This page explains what CJC-1295 (no-DAC) is and where it came from — the science and the story — not who should use anything, or how. These are research materials for laboratory research only; nothing here is medical, dosing, or treatment advice.

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