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Research monograph · modified grf(1-29), protease-resistant synthetic ghrh(1-29) analog (no albumin-binding dac)
CJC-1295Research monograph
GH Half-Life Studies
This monograph collects what the published literature reports about CJC-1295 — its mechanisms, the areas it is studied in, its molecular record and the sources behind them. Each substitution targets a site where enzymes would otherwise cleave the sequence, extending how long the molecule survives in circulation compared with unmodified GHRH. Research measures growth hormone release profiles and the shape of the resulting pulse.
For laboratory research use only — not for human or animal use
Mechanisms
How CJC-1295 works
GHRH Receptor Activation
GHRH-R Agonist
Four substitutions — at positions 2, 8, 15 and 27 — each block a site where enzymes would cleave native GHRH(1-29). The receptor interaction is unchanged; only the molecule's survival time is.
Selective for the GHRH receptor
Position-2 substitution blocks DPP-IV cleavage
Binds pituitary somatotrophs at high affinity
Pulsatile GH Secretion
Pulsatile GH
A roughly thirty-minute half-life produces discrete pulses rather than the sustained elevation the DAC variant gives. That difference is the reason both versions exist and are studied separately.
Half-life around 30 minutes without albumin binding
Produces discrete rather than sustained release
Peak response within 15-30 minutes
GH/IGF-1 Axis Stimulation
IGF-1 Axis
Each pulse drives a transient rise in hepatic IGF-1. Because exposure is brief, the IGF-1 profile differs markedly from the prolonged elevation reported with the DAC variant.
IGF-1 rises transiently with each pulse
Cortisol and prolactin unaffected
Studied alongside ghrelin-receptor secretagogues
Studied applications
What CJC-1295 is researched for
Endocrinology
Pulsatile GH Research
The short half-life is the feature here: it produces discrete pulses, which is what makes the compound useful for studying release pattern rather than total exposure.
Teichman et al. 2006
Pharmacology
GHRH Analog Comparison
Most often studied head-to-head against the DAC variant, where the only meaningful variable is duration of action.
Frohman et al. 2003
Combination Research
CJC / Ipamorelin Synergy
Combination work pairs it with a ghrelin-receptor agonist to test whether engaging two receptor populations amplifies the pulse.
Raun et al. 1998
Animal Models
GHRH Axis Restoration
Animal models examine whether upstream stimulation restores a release pattern closer to normal physiology than exogenous growth hormone does.
Alba et al. 2006
What the published work measures
The endpoints reported across the literature for this compound. The figures belong to the individual papers, not to us.
Half-Life vs Native GHRH(1-44)
DPP-IV Protease Resistance
GHRH-R Binding Affinity vs Native GHRH
Selectivity — Cortisol / Prolactin Effect
Reference values
CJC-1295 molecular data
Scroll for full molecular data →
Molecular weight
3,367.97 g/mol
Molecular formula
C152H252N44O42
Physical form
Lyophilized Powder
Documented purity
Quantified by HPLC, reported per lot
Storage
-20°C for up to 24 months
Solubility
Water-soluble
Available sizes
5mg
FAQ
Common questions about CJC-1295
What is CJC-1295?
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CJC-1295 without DAC is a modified GHRH fragment carrying four amino acid substitutions. Each substitution targets a site where enzymes would otherwise cleave the sequence, extending how long the molecule survives in circulation compared with unmodified GHRH. Research measures growth hormone release profiles and the shape of the resulting pulse.
What is CJC-1295 researched for?
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Published research on CJC-1295 concentrates on Pulsatile GH Research, GHRH Analog Comparison, CJC / Ipamorelin Synergy and GHRH Axis Restoration. Each of those areas is summarised further up this page with the citation it comes from, and the full reference list — 4 indexed publications — sits at the bottom. Study designs and concentrations vary considerably between publications, so the primary sources are worth reading directly.
How does CJC-1295 work?
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The literature describes CJC-1295 acting across GHRH Receptor Activation, Pulsatile GH Secretion and GH/IGF-1 Axis Stimulation, reported respectively as GHRH-R Agonist, Pulsatile GH and IGF-1 Axis. Those pathways are drawn from preclinical models rather than clinical work, and they describe what has been observed rather than a settled mechanism — the individual pathway cards above cite what each one is based on.
What are the molecular specifications for CJC-1295?
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CJC-1295 has a molecular formula of C152H252N44O42 and an average mass of 3367.97 g/mol. It is indexed under CAS 863288-34-0. It ships as lyophilized powder. Those are nominal reference values for the parent compound. The identity of the specific material you receive is confirmed by mass spectrometry and reported on that lot's certificate.
How should CJC-1295 be stored and reconstituted?
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Store the sealed vial at -20°C, protected from light and moisture, and let it reach room temperature before opening so condensation does not form on cold powder. CJC-1295 is water-soluble; reconstitute by directing the diluent down the vial wall rather than onto the powder, then swirl to dissolve rather than shaking. Keep reconstituted solution refrigerated and avoid repeated freeze-thaw cycles — solutions are far less stable than lyophilized powder.
Is CJC-1295 approved for human use?
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No. CJC-1295 is supplied strictly for in-vitro laboratory research and development. It is not a drug, food, supplement or cosmetic, it has not been evaluated by the FDA, and it is not intended for human or animal consumption, ingestion, injection or any in-vivo use. Ordering confirms you are a qualified researcher or institution purchasing on that basis.
Cited sources
Peer-reviewed literature
Independent published research indexed from PubMed — not Routine Peptides claims.
Every production run is analyzed by an independent laboratory, and the certificate for your lot travels with the order — not a catalog-wide document, and not a summary written by us.