If you have been reading about CJC-1295 and want a single page that covers the useful parts, this is it: definitions, context, how it is studied, and the questions that come up repeatedly.
Last reviewed on 2026-05-26. Where a claim depends on a specific study, the study is described rather than over-claimed.
The core sequence keeps the receptor-binding region of GHRH while replacing four positions that are vulnerable to dipeptidyl peptidase-4 and other proteases. Substitutions at positions 2, 8, 15, and 27 raise metabolic stability relative to the natural hormone. The N-terminal residues remain essential for activity, so changes there generally lower potency. Molecular weight sits near 3368 daltons for the tetrasubstituted analog without the linker, while the albumin-binding form is heavier because of the added maleimide group.
CJC-1295 is a synthetic peptide modeled on growth hormone-releasing hormone, the hypothalamic signal that prompts the pituitary to release growth hormone. Its sequence corresponds to the first twenty-nine residues of human GHRH, with four substitutions that slow enzymatic breakdown. Early descriptions placed the compound in research on growth hormone deficiency and related conditions, and later literature groups it with the long-acting GHRH analogs. The name appears in both laboratory and popular fitness writing, where it sometimes labels chemically different peptides.
The drug affinity complex is a maleimidopropionic acid group attached to a lysine side chain. It reacts with the free thiol of cysteine-34 on circulating albumin, forming a covalent bond. This conjugation keeps the peptide in the bloodstream and shields it from rapid renal filtration and proteolysis. Reported circulation half-lives for the albumin-bound form fall in the range of roughly six to nine days in early human studies.
Binding to GHRH receptors on pituitary somatotroph cells triggers cyclic AMP signaling and stimulates growth hormone synthesis and release. Because the peptide acts upstream of the pituitary, effects are mediated through endogenous growth hormone rather than direct receptor activation in peripheral tissues. Increases in insulin-like growth factor 1 are generally described as a downstream consequence. Most published human exposure data come from small early-stage studies, and the clinical significance of the pharmacokinetic profile remains incompletely characterized.
| Property | Value | Notes |
|---|---|---|
| Class | Synthetic peptide | GHRH receptor agonist |
| Sequence length | 29 amino acids | Derived from human GHRH |
| Molecular weight | About 3368 Da without linker | Albumin-binding form is heavier |
| Appearance | White to off-white lyophilized powder | Common form for research reference material |
| Typical storage | -20 °C or below, desiccated | Protect powder from light and moisture |
Identity and purity are established with reversed phase high performance liquid chromatography coupled to mass spectrometry. The chromatographic step separates the target peptide from truncated sequences and deletion products, while the mass measurement confirms the expected molecular weight to within a fraction of a dalton. Because the two common variants differ by the presence of the linker, mass alone can distinguish them in the unconjugated state. Amino acid analysis and peptide mapping are used when sequence level confirmation is required.
Lyophilized material is generally stable for extended periods when held at minus twenty degrees Celsius or below and protected from moisture and light. In solution the peptide is more labile; bond hydrolysis, aggregation and oxidation of susceptible residues all proceed faster at ambient temperature. Repeated freeze and thaw cycles should be avoided because they promote clumping and loss of soluble material. The conjugated variant adds a further consideration, since the maleimide group can hydrolyze in aqueous buffer and lose its ability to react with albumin.
Clearance profiles diverge sharply between the two versions. The albumin-binding molecule stays in plasma for several days, whereas the unmodified analog is largely gone within about half an hour in reported work. Cleavage by dipeptidyl peptidase IV is a major contributor to the short life of the unmodified sequence. These gaps mean the two versions cannot be substituted for each other in study design or in reading results side by side.
Reports on this compound commonly follow serum growth hormone and insulin-like growth factor 1 across defined time windows. Protocols differ in sampling frequency, assay platform, and participant characteristics, which makes direct comparison between publications difficult. Some work focuses on pulsatile release patterns instead of average concentrations. Whether repeated exposure alters endogenous hormone rhythms over long periods remains an open question, and the formal literature is thinner than the volume of informal commentary implies.
Once in circulation, the peptide binds the growth hormone-releasing hormone receptor displayed on pituitary somatotroph cells. Receptor activation couples to Gs proteins, elevates intracellular cyclic AMP, and drives protein kinase A signaling inside the cell. That cascade increases discharge of growth hormone into the bloodstream. The analog therefore operates through a receptor pathway that already exists for the body's own releasing hormone, rather than through an engineered artificial target.
== Articles == Hoyle, F. and Wickramasinghe, N.C., 1962. On graphite particles as interstellar grains, Mon.Not.Roy.Astr.Soc. 124, 417-433 Hoyle, F.; Wickramasinghe, N.C. (1969). "Interstellar Grains". Nature. 223 (5205): 450–462. Bibcode:1969Natur.223..459H. doi:10.1038/223459a0. S2CID 4209522. Wickramasinghe, N. C. (1974). "Formaldehyde polymers in interstellar space". Nature. 252 (5483): 462–463. doi:10.1038/252462a0. ISSN 0028-0836. Retrieved 20 January 2026. Wickramasinghe, N.C. (1999). "Formaldehyde Polymers in Interstellar Space". Astrophysics and Space Science. 268 (1–3): 111–114. doi:10.1023/A:1002448820097. ISSN 0004-640X. Retrieved 20 January 2026. Wickramasinghe, N.C.; Hoyle, F.; Brooks, J.; Shaw, G. (1977). "Prebiotic polymers and infrared spectra of galactic sources". Nature. 269 (5630): 674–676. Bibcode:1977Natur.269..674W. doi:10.1038/269674a0. S2CID 4266722. Hoyle, F. and Wickramasinghe, N.C., 1977. Identification of the λ2,200A interstellar absorption feature, Nature 270, 323-324 F., Hoyle; N. C., Wickramasinghe (4 November 1976). "Primitive grain clumps and organic compounds in carbonaceous chondrites" (PDF). Nature. 264 (5581): 45–46. Bibcode:1976Natur.264...45H. doi:10.1038/264045a0. Retrieved 18 January 2013. Hoyle, F. and Wickramasinghe, N.C., 1977. Polysaccharides and infrared spectra of galactic sources, Nature 268, 610-612 Hoyle, F.; Wickramasinghe, N.C. (1979). "On the nature of interstellar grains". Astrophysics and Space Science. 66 (1–3): 77–90. Bibcode:1999Ap&SS.268..249H. doi:10.1023/A:1002462602776. S2CID 189820472.
Choh Hao Li (sometimes Cho Hao Li) (Chinese: 李卓皓; pinyin: Lǐ Zhuōhào; April 21, 1913 – November 28, 1987) was a Chinese-born American biochemist who discovered in 1966 that human pituitary growth hormone (somatotropin) consists of a chain of 256 amino acids. In 1970, he succeeded in synthesizing this hormone, the largest protein molecule synthesized up to that time.
Alvin America "Eric" Tao (Ken Leung) is a MD on Pierpoint’s CPS desk and one of the series’ protagonists. A longtime Pierpoint executive, Eric is brilliant, volatile, and ruthlessly pragmatic, frequently crossing ethical lines in pursuit of power. He takes Harper Stern on as a protégé, recognizing her ambition as a reflection of his own. Eric rose through the firm’s New York headquarters under the late MD Newman, remaining conflicted between admiration for Newman and the racism Newman directed at him. Eric is longtime friends with global head of FICC Bill Adler, whom he once hired and who later surpassed him in rank. He is married to Candice Allbright with two daughters, Lily and Lara. In series 1, Eric salvages a disastrous trade Harper executes and admits he knows she never graduated from college but does not care. His relationship with key client Felim Bichan collapses after Eric makes offensive remarks in front of Felim’s wife. When Harper fails to recover the account, Eric traps and berates her in a conference room, prompting Daria Greenock to push Harper to report him, leading to Eric’s firing. On reduction-in-force day, Adler convinces Harper to retract her complaint to reinstate Eric, resulting in Daria’s dismissal. In series 2, Eric briefly regains Felim as client, only to lose him permanently after Harper goes behind Eric's back to sell a controlling stake in healthcare startup Rican to Jesse Bloom, which Eric had promised to Felim. Adler confronts Eric over sustained underperformance, sidelines him from the trading floor, and relegates him to a marginal role.
=== Reflection of the target molecule === The first step is the production of the target's enantiomer. In the case of peptides and small proteins that are produced synthetically, an enantiomer is made using synthetic D-amino acids. If the target is a larger protein molecule, beyond synthetic abilities, the enantiomer of an epitope is produced.
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Natural GHRH is degraded quickly by dipeptidyl peptidase-4 and related enzymes, giving it a half-life measured in minutes. CJC-1295 carries substitutions that slow that breakdown, so it stays intact longer. Both act at the same pituitary receptor and produce the same class of signal.
The label was first attached to the albumin-binding form during early development work. A shorter analog without the linker later became known by the same name in informal use. Published papers normally state which version was studied, so the methods section resolves the ambiguity.
It is a synthetic peptide rather than a steroid, and it does not occur naturally in the body. Its sequence is derived from a hypothalamic hormone called growth hormone-releasing hormone. It works as a receptor agonist rather than as a replacement for that hormone.
The two share the same 29-amino-acid backbone. CJC-1295 carries an additional albumin-binding moiety that markedly extends its residence time in circulation, while the form without that moiety clears faster. Literature sometimes applies the name loosely to either variant.