ARA 290 Peptide (Cibinetide) 10mg

ARA-290 (Cibinetide) 10mg is a synthetic 11-amino-acid research peptide derived from the helix B region of erythropoietin (EPO). Supplied as a lyophilized powder, each vial is third-party tested for purity and identity, with a Certificate of Analysis available. For research and laboratory use only. Not for human or veterinary use.

  • 10mg lyophilized powder
  • HPLC & MS verified
  • COA included
  • Fast shipping

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SKU OML-ARA-290-10mg Category
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Verified. This product cleared third-party testing.

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Purity :

99.66% (per batch COA)

Form :

Lyophilized powder

Size :

10mg

Storage :

-20°C (lyophilized), 4°C (reconstituted)

Batch :

OML-Z-26210

Our Third-Party Testing Commitment

Overmatch Labs does not sell any compound or peptide that has not passed independent third-party laboratory testing at 99%+ purity. Every batch is tested by an accredited third-party laboratory — not our own facility — to ensure unbiased verification of identity, purity, and endotoxin levels. We believe transparent, verifiable science is the foundation of trust.

Description

What Is ARA 290 Peptide?

ARA 290 peptide, also known by its international nonproprietary name Cibinetide, is a synthetic linear peptide of 11 amino acids modeled on the three-dimensional structure of helix B of erythropoietin. Unlike EPO, ARA-290 was designed so that it does not stimulate red blood cell production in research models. Instead, it was developed to selectively engage the innate repair receptor (IRR), a heteromeric complex of the EPO receptor and the β-common receptor (CD131).

Because of this selective receptor activity, the ARA 290 peptide has become a subject of interest in preclinical and clinical research on tissue protection, inflammation signaling, and peripheral nerve function.

ARA 290 Peptide Research Overview

ARA-290 has been studied in published scientific literature in the following areas:

  • Small fiber neuropathy research: Phase 2 clinical studies looked at cibinetide in subjects with sarcoidosis-associated small fiber neuropathy, measuring corneal nerve fiber density and neuropathic symptom scores.
  • Metabolic and diabetic neuropathy models: Research investigated ARA-290 in type 2 diabetes-associated neuropathy and metabolic markers.
  • Nerve regeneration and tissue repair: Preclinical studies explored the peptide’s role in IRR-mediated anti-inflammatory and tissue-protective signaling.

These summaries describe published research only. They are not claims of therapeutic benefit. This product is not intended to diagnose, treat, cure or prevent any disease.

Certificate of Analysis Document

Detailed purity verification and batch analysis results

Research

Scientific research related to this compound

References

Citations and reference materials

Mechanism of Action

How this compound works at a biological level

In published research, ARA-290 (Cibinetide) has been investigated for mechanisms including: ARA-290 is an 11-amino acid peptide derived from the helix-B surface domain of erythropoietin (EPO). It selectively binds the innate repair receptor, a heterodimer of the EPO receptor and the β-common receptor (CD131), which is expressed on injured and inflamed tissue rather than on erythroid progenitors. Because it does not engage the homodimeric EPO receptor, it has been studied for tissue-protective and anti-inflammatory signalling without the red-blood-cell-stimulating activity of EPO. Mechanistic descriptions reflect findings in laboratory and animal-model research only.

Technical Details

Specifications, properties, and technical data

  • Compound type: Single
  • CAS number: 1208243-50-8
  • PubChem CID: 91810664 (https://pubchem.ncbi.nlm.nih.gov/compound/91810664)
  • Physical form: Lyophilized powder
  • Purity: ≥ 99% (HPLC; see batch Certificate of Analysis)
  • Size: 10mg
  • Storage: -20°C (lyophilized), 4°C (reconstituted)
  • Handling notes: Lyophilized: Store at −20°C for long-term stability; keep dry and protected from light. Reconstituted: Refrigerate at 2–8°C; use within 3–4 weeks. Avoid repeated freeze–thaw cycles. Allow vials to reach room temperature before opening to reduce condensation uptake.

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