A modified GHRH(1-29) analogue engineered for improved proteolytic stability via Ala2 → D-Ala and substitutions at positions 8, 15, 27. Lacks the Drug Affinity Complex (DAC) maleimide linker, yielding a shorter-acting profile than CJC-1295 DAC. Used in pulsatile GH axis research requiring defined, time-limited stimulation.
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CJC-1295 without DAC is a synthetic GHRH(1-29) analogue engineered with four amino acid substitutions to improve resistance to DPP-IV and serine protease cleavage relative to native GHRH. The modifications include D-Ala at position 2, Gln at 8, Ala at 15, and Leu at 27, each selected to block common proteolytic cleavage sites while preserving GHRHR binding affinity.
Unlike CJC-1295 with DAC (which contains a maleimide moiety that covalently binds serum albumin to extend half-life), the no-DAC form lacks this attachment chemistry. As a result, it has a shorter plasma half-life in animal models, providing a pharmacological tool for studying the GH axis response to intermittent GHRH stimulation without the continuous receptor engagement associated with the albumin-bound form.
In vitro and animal research has used CJC-1295 (no DAC) alongside sermorelin and the DAC form to characterize the differential effects of brief vs. sustained GHRH receptor stimulation on pituitary somatotroph desensitization, GH pulse amplitude, and IGF-1 production kinetics. It is commonly co-administered with GHRP-2 or ipamorelin in synergistic GH axis research protocols.
All referenced studies are preclinical or in vitro. Not for human use.
| Full Name / IUPAC | CJC-1295 (No DAC) |
| CAS Number | 863288-34-0 |
| Molecular Formula | C₁₅₂H₂₅₂N₄₄O₄₂ |
| Molecular Weight | 3,367.9 g/mol |
| Sequence / Structure | GHRH(1-29) modified: D-Ala2, Gln8, Ala15, Leu27 substitutions; C-terminal amide |
| Appearance | White lyophilized powder |
| Solubility | Soluble in sterile water or 0.1% acetic acid |
| Format | Lyophilized (freeze-dried) powder |
| SKU | CL-034 |