ARA 290 vs Semax
ARA 290 and Semax are studied in overlapping research areas, which is why they are frequently compared. This is a neutral side-by-side reference drawn from published preclinical literature and laboratory handling data.
How they actually differ
Comparing the two: ARA 290 is 11-amino-acid epo-derived linear peptide, while Semax is synthetic heptapeptide, acth(4-7) analogue — different molecular classes with different handling consequences; they call for different primary diluents (bacteriostatic water (0.9% benzyl alcohol) versus sterile or bacteriostatic water); their leading degradation routes differ (asparagine/glutamine deamidation is the most plausible slow route for this sequence. for ARA 290, n-terminal methionine oxidation to the sulfoxide for Semax), so the storage precautions that matter are not the same; their practical working windows differ once reconstituted. The sections below set out each in full.
ARA 290 — origin
ARA 290 (Cibinetide) is an 11-residue peptide modelled on the helix-B surface of erythropoietin. It was engineered to engage the innate repair receptor — a heteromer of the EPO receptor and the beta-common receptor — without the erythropoietic (red-blood-cell-stimulating) activity of full-length EPO.
Semax — origin
Semax was developed at the Institute of Molecular Genetics in Moscow by attaching the Pro-Gly-Pro tripeptide to the ACTH(4-7) fragment. That C-terminal addition is the entire design rationale: it confers resistance to the aminopeptidases that clear the parent fragment within seconds, without retaining the corticotropic activity of full-length ACTH.
ARA 290 research themes
Studied for selective engagement of the EPOR/beta-common receptor heteromer that mediates tissue-protective signalling, distinct from the classical erythropoietic receptor.
A substantial share of the published literature examines small-fibre and neuropathic-pain research models.
Investigated for modulation of inflammatory pathways in preclinical tissue-injury models.
Semax research themes
One of the most-cited research findings is upregulation of brain-derived neurotrophic factor in animal models.
A substantial Russian literature examines the compound in cerebral ischemia models.
Investigated in behavioural models measuring attention and memory consolidation.
The ACTH(4-7) fragment was selected specifically because it lacks the hormonal activity of the full sequence.
ARA 290 handling
- Reach room temperature before opening the vial.
- Add diluent gently down the vial wall; do not vortex.
- Use low-bind labware at low working concentrations to limit adsorption.
Semax handling
- Use amber vials or store in the dark; this is a light-sensitive compound by virtue of its N-terminal methionine.
- For nasal-spray research formats, treat the reconstituted solution as a multi-use container and observe the preserved-diluent window.
- Do not warm to accelerate dissolution — it is unnecessary at this molecular weight and adds thermal exposure.
Both third-party tested
Every Popular Peptides batch of ARA 290 and Semax is independently tested by HPLC and LC-MS with a published Certificate of Analysis. Enter a lot number to pull the COA for a specific vial.
ARA 290 reference
Related comparisons
ARA 290 and Semax are supplied strictly as research chemicals for in-vitro laboratory and research use only. They are not intended for human or animal consumption, diagnostic, or therapeutic use. This comparison summarizes published preclinical literature and laboratory handling data; it is not medical advice, not a claim of efficacy, and not usage guidance.