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≥99% PurityARA-290 vial

ARA-290

An EPO-derived peptide studied for calming inflammation and nerve repair

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About this compound

ARA-290 is also called cibinetide. It is a peptide made of 11 amino acids, taken from one section of erythropoietin. That is the hormone that drives red blood cell production. ARA-290 was designed to keep the tissue repair signaling while leaving out the red blood cell effect. Research has measured its activity at the innate repair receptor, a two-part receptor complex, and examined nerve and inflammation endpoints.

EPO helix-B surface derived 11-amino-acid peptide

Formula
C55H89N19O20
Molecular weight
1257.3 g/mol
Form
Lyophilized powder
CAS / ID
1208243-50-8
Read the full ARA-290 research monograph
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Amino Acids
EPO helix-B derived peptide
0
Molecular Weight (Da)
C55H89N19O20
0+
Human Trials
sarcoidosis small-fiber neuropathy
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Research Areas
Sarcoidosis Small-Fiber Neuropathy · Corneal & Skin Nerve Fiber Regrowth · Long-Term Allodynia Relief & more
How It Works

How ARA-290 works

The pathways ARA-290 acts on — and what each one does. The animation traces its signal outward from the compound to every target it engages.

Signalling pathways studied in preclinical models · illustrative
IRR (EPOR/CD131) Agonism
Innate Repair Receptor

ARA-290 (cibinetide) is an 11-amino-acid peptide engineered from the helix-B surface of erythropoietin (EPO). It selectively activates the innate repair receptor (IRR) — a heterocomplex of the EPO receptor and the β-common receptor (CD131) — the tissue-protective arm of EPO signaling, without engaging the classical receptor that drives red-cell production.

  • Selective IRR (EPOR/βcR) agonism
  • Non-erythropoietic — no effect on hematocrit
  • Mimics EPO's helix-B tissue-protective domain
Resolution of Inflammation
Anti-Inflammatory

Through the innate repair receptor, ARA-290 dampens pro-inflammatory signaling and promotes its resolution, reducing collateral tissue damage from the injury and immune response — a mechanism characterized in both preclinical and clinical research.

  • Suppresses pro-inflammatory cytokine signaling
  • Shifts macrophages toward a reparative phenotype
  • Suppresses spinal microglial activation in pain models
Cytoprotective & Neuroregenerative Signaling
Tissue Protection

IRR activation engages JAK2/STAT3, PI3K/Akt, and anti-apoptotic Bcl-2-family pathways, supporting cell survival and small-nerve-fiber regeneration despite the peptide's very short plasma half-life.

  • Activates JAK2/STAT3 & PI3K/Akt survival signaling
  • Anti-apoptotic Bcl-2 family engagement
  • Associated with small-fiber nerve regrowth in research
Uses & Applications

What ARA-290 is researched for

The main areas ARA-290 is being studied for — and the study-reported figures behind them.

Neuropathic Pain

Sarcoidosis Small-Fiber Neuropathy

In a randomized, double-blind pilot study, ARA 290 improved small-fiber neuropathy symptom scores and physical functioning in sarcoidosis patients, with no safety concerns.

Heij et al. 2012
Nerve Regeneration

Corneal & Skin Nerve Fiber Regrowth

28 days of ARA 290 significantly improved neuropathic symptoms and initiated regrowth of small nerve fibers, including increased corneal nerve fiber density.

Dahan et al. 2013
Preclinical Pain

Long-Term Allodynia Relief

In rodent models, ARA 290 dose-dependently reduced mechanical and cold allodynia for up to 20 weeks, coupled with suppression of the spinal microglia response.

Swartjes et al. 2014
Tissue Protection

EPO-Derived Cytoprotection

ARA 290 was engineered from EPO's tertiary structure to deliver tissue-protective and anti-inflammatory effects via the innate repair receptor, without stimulating erythropoiesis.

Brines et al. 2008

Study-reported magnitudes

Representative figures from published research. Bars fill as you scroll.

Biological effect duration24–72 h
Plasma half-life~2 min
Effect on red blood cell productionNone

Figures are representative of published research findings and shown for reference.

Molecular Structure

The ARA-290 molecule

An interactive 3D model rendered from the compound record — rotate and explore its structure.

C55H89N19O20

Molecular formula
C55H89N19O20
Molecular weight
1257.3 g/mol
Sequence length
11 residues
CAS / ID
1208243-50-8
Physical form
Lyophilized powder
Documented purity
≥99% by HPLC
Third-Party Verified

Independently tested. Verifiably pure.

Every batch of ARA-290 is sent to an accredited independent laboratory before it ships. Here is what we screen for.

  • HPLC Purity AnalysisConfirms the peptide is ≥99% pure
  • Mass SpectrometryVerifies the exact molecular identity
  • Heavy Metals ScreeningLead, arsenic, cadmium & mercury — Pass
  • Endotoxins (LAL)Bacterial endotoxin levels — Pass
  • Sterility TestingNo microbial contamination — Pass
  • Net Peptide ContentActual peptide mass per vial verified
Certificate of Analysis · Freedom DiagnosticPASS
HPLC Purity
≥99%
Identity
Mass-spec confirmed
Endotoxin (LAL)
Pass
Net content
Verified
Browse the COA Library
Compound Information

Full specification

Chemical NameARA-290 (Cibinetide)
SequencepGlu-Glu-Gln-Leu-Glu-Arg-Ala-Leu-Asn-Ser-Ser (11 aa)
Molecular Weight1,257.3 Da
Molecular FormulaC₅₅H₈₉N₁₉O₂₀
CAS Number1208243-50-8
FormLyophilized powder
Purity≥99% (HPLC verified)
TestingThird-party HPLC, Mass Spec, Endotoxin
Storage-20°C for long-term stability
SolubilitySterile or bacteriostatic water
COAIncluded with every order
FAQ

Common questions about ARA-290

ARA-290 (cibinetide) is a synthetic 11-amino-acid peptide engineered from the helix-B surface domain of erythropoietin (EPO). It was designed to activate EPO's tissue-protective, anti-inflammatory signaling through the innate repair receptor — without the red-blood-cell-stimulating activity of native EPO.

The IRR is a heterocomplex of the EPO receptor and the β-common receptor (CD131). It mediates EPO's protective and regenerative effects in tissue, distinct from the classical homodimeric EPO receptor that controls erythropoiesis. ARA-290 selectively activates this repair receptor.

No. ARA-290 is non-erythropoietic — it does not engage the receptor pathway that drives red-cell production, so it does not raise hematocrit. That separation of tissue protection from erythropoiesis is the central rationale behind its design.

Phase 2 studies in sarcoidosis-associated small-fiber neuropathy reported improved neuropathic symptom scores, increased corneal nerve fiber density, and regrowth of small nerve fibers, with a favorable safety profile. Preclinical models also show long-term reduction of neuropathic pain behaviors.

No. Research-grade ARA-290 sold here is strictly for in vitro laboratory research and analytical applications. It is not a drug and is not intended for human or veterinary use, consumption, or any clinical application.

For Research Use Only.

Not for human or veterinary use. For in-vitro laboratory research only. These statements have not been evaluated by the FDA; this product is not intended to diagnose, treat, cure, or prevent any disease. Sold exclusively to qualified researchers and institutions.