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Cjc-1295 Structure And Mechanism — Deep Dive

By Editorial Desk · published 2025-11-23 · last reviewed 2025-12-12 · Wiki

RP-HPLC raises a handful of sensible questions. This page answers them in order, starting with the fundamentals and moving to applications.

Reviewed 2025-12-12. Anything still debated is marked as such rather than presented as settled.

CJC-1295 Structure And Mechanism

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.

CJC-1295 is a synthetic analogue of growth hormone-releasing hormone, built on the 29-amino-acid GHRH(1-29) fragment. Four substitutions distinguish it from the natural sequence: D-alanine at position 2, glutamine at position 8, alanine at position 15, and leucine at position 27. These changes reduce enzymatic cleavage and extend the peptide's persistence in circulation. The compound is discussed in two forms, one carrying a drug affinity complex and one without it.

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.

Handling, Stability and Analysis

Reported half-lives differ widely between the two variants and between species. Values for the albumin-binding form are usually expressed in days, while the unconjugated form is measured in minutes to a few hours. Sampling schedules, assay sensitivity, and route of administration all influence the numbers, which limits direct comparison across studies. Whether sustained receptor occupancy produces different downstream effects from pulsatile stimulation remains an open question in the published work. Claims about relative potency should therefore be read alongside the specific study design that produced them.

Lyophilised powder is the usual supplied form. The material is hygroscopic, so vials are typically equilibrated to room temperature before opening in order to prevent condensation on the contents. Long-term storage is generally described at minus twenty degrees Celsius or colder, protected from light and moisture. Repeated freeze-thaw cycles are avoided because they promote aggregation and loss of soluble material. A reconstituted solution is considerably less stable than the dry powder and is normally kept refrigerated for short periods only.

Cjc-1295 at a glance

PropertyValueNotes
Physical formLyophilized white powderSupplied as a freeze-dried solid for research use
Molecular weightApproximately 3,647 Da (DAC form)Lower for the variant lacking the albumin-binding moiety
SolubilitySoluble in water and aqueous bufferTypically dissolved in sterile or bacteriostatic water
Typical storage temperature−20 °C or belowDry powder, desiccated and protected from light
Common analytical methodReversed-phase HPLC with mass spectrometryUsed for purity estimation and identity confirmation

Molecular Background and Naming

Two related forms circulate in technical discussion under the same family name. The original version carries a drug affinity complex (DAC) that binds covalently to serum albumin after administration, and this linkage substantially extends circulation time. A second form, frequently written as modified GRF(1-29) or CJC-1295 without DAC, lacks that linker and clears much faster. The naming is a frequent source of confusion because the shorthand CJC-1295 can refer to either form depending on the source. Reports sometimes fail to specify which variant was studied.

The peptide backbone includes a D-alanine at position two, which resists cleavage by dipeptidyl peptidase IV, and several other substitutions that reduce degradation. Its molecular weight is roughly 3.4 kDa without the linker and about 3.6 kDa with it. The molecule is water soluble and is normally supplied as a lyophilized powder. Precise sequence and mass values depend on which variant is described, so technical documents usually state the exact form being referenced.

CJC-1295 is a synthetic peptide designed as a long-acting analogue of growth hormone-releasing hormone (GHRH). Its structure derives from the first 29 amino acids of native GHRH, a fragment often called GRF(1-29). Four substitutions were introduced to slow enzymatic breakdown and extend activity relative to the natural sequence. The compound was developed by ConjuChem as part of a broader effort to improve the pharmacokinetic profile of peptide hormones. It is studied in laboratory and clinical research settings rather than appearing as a naturally occurring substance.

Related pages on this site

Background and Molecular Design

The second form adds a maleimide-bearing linker to the lysine at the carboxyl end. This group reacts with cysteine-34 on circulating serum albumin, forming a covalent bond that keeps the peptide in the bloodstream for far longer. ConjuChem developed the molecule as a way to extend the action of a peptide without frequent administration. The albumin attachment is the defining structural feature of the drug affinity complex version. Whether continuous exposure produces effects distinct from shorter pulses remains an unresolved research question.

Supporting material

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There are also dimeric alkaloids formed from two distinct monomers, such as the vinca alkaloids vinblastine and vincristine, which are formed from the coupling of catharanthine and vindoline. The newer semi-synthetic chemotherapeutic agent vinorelbine is used in the treatment of non-small-cell lung cancer. It is another derivative dimer of vindoline and catharanthine and is synthesised from anhydrovinblastine, starting either from leurosine or the monomers themselves.

Sources: en.wikipedia.org

Supporting material

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Kripke explained that Soldier Boy was Vought's version of Wayne since he worked for them for several decades and is someone who comes from a different era, but still has the ego and ambition for which he described him as the "Homelander before Homelander." Many of the changes were applied to give Homelander a threat just as he is finally starting to take control of Vought, but Kripke wanted to ensure that it was someone that the character has never faced before with someone that has the same strength as him and could actually fight him, for which he considered Soldier Boy to be the best match. Besides introducing Soldier Boy, the season also introduces the superhero team Payback for which the character was leader. Unlike in the comics where the team served as a rival of the Seven, Payback has already disbanded by the time where the series take place; it used to be the world's premiere team of supes before the Seven was formed and is described as "the Seven before the Seven." Kripke explained that the changes were mostly done to get a deeper exploration of Vought's history by exploring the past of each member of the teams, so the writers are allowed to shed light on the show's present. The season also includes a storyline focused mostly on Kimiko Miyashiro. As the season progresses, Kimiko goes through an emotional arc for which she starts learning to express herself after spending most of her life doing what other people wanted.

=== Journal articles === Bridge, D; Cunningham, C W; Schierwater, B; DeSalle, R; Buss, L W (15 September 1992). "Class-level relationships in the phylum Cnidaria: evidence from mitochondrial genome structure". Proceedings of the National Academy of Sciences. 89 (18): 8750–8753. Bibcode:1992PNAS...89.8750B. doi:10.1073/pnas.89.18.8750. PMC 49998. PMID 1356268. Bridge, D; Cunningham, CW; DeSalle, R; Buss, LW (July 1995). "Class-level relationships in the phylum Cnidaria: molecular and morphological evidence". Molecular Biology and Evolution. 12 (4): 679–689. doi:10.1093/oxfordjournals.molbev.a040246. PMID 7659022. Fautin, Daphne Gail (October 2002). "Reproduction of Cnidaria". Canadian Journal of Zoology. 80 (10): 1735–1754. Bibcode:2002CaJZ...80.1735F. doi:10.1139/z02-133. hdl:1808/5373. Mackie, G O (October 2002). "What's new in cnidarian biology?". Canadian Journal of Zoology. 80 (10): 1649–1653. Bibcode:2002CaJZ...80.1649M. doi:10.1139/z02-138. Schuchert, P. (27 April 2009). "Phylogenetic analysis of the Cnidaria". Journal of Zoological Systematics and Evolutionary Research. 31 (3): 161–173. doi:10.1111/j.1439-0469.1993.tb00187.x. Kass-Simon, G; Scappaticci, Jr., A A (October 2002). "The behavioral and developmental physiology of nematocysts". Canadian Journal of Zoology. 80 (10): 1772–1794. Bibcode:2002CaJZ...80.1772K. doi:10.1139/z02-135. J. Zrzavý (2001). "The interrelationships of metazoan parasites: a review of phylum- and higher-level hypotheses from recent morphological and molecular phylogenetic analyses". Folia Parasitologica. 48 (2): 81–103.

Sources: en.wikipedia.org

Supporting material

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Ergothioneine (EGT) is a naturally occurring amino acid and is a thiourea derivative of histidine, containing a sulfur atom on the imidazole ring. This compound occurs in relatively few organisms, notably actinomycetota, cyanobacteria, and certain fungi. Ergothioneine was discovered by Charles Tanret in 1909 and named after the ergot fungus from which it was first purified, with its structure being determined in 1911. Unlike other ergot alkaloids, ergothioneine is not an ergoline derivative. In humans, ergothioneine is acquired exclusively through the diet and accumulates in erythrocytes, bone marrow, liver, kidney, seminal fluid, and eyes. Although the effect of ergothioneine in vivo is under preliminary research, its physiological role in humans is unknown. Ergothioneine is sold as a dietary supplement.

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Sources: en.wikipedia.org

Frequently asked questions

How does CJC-1295 differ from modified GRF(1-29)?

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.

Is CJC-1295 an approved medicine?

It has not been approved by major regulatory agencies for any therapeutic indication. Material sold under this name is typically distributed for laboratory research only. Clinical use is not supported by large controlled trials.

What is known about its half-life?

Early human studies of the albumin-binding form reported circulation half-lives on the order of several days. The value depends on assay method and study design. Estimates for the form without the binding moiety are considerably shorter.

Why is mass spectrometry used alongside chromatography?

Chromatography reports how much material elutes as a single peak but does not confirm what that material is. Mass spectrometry supplies the molecular mass, which is characteristic of a given sequence and its modifications. Together the two methods support both a purity figure and an identity claim.

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