ARA-290 (Cibinetide) Peptide – Premium Innate Repair Receptor Agonist for Research
ARA-290 (Cibinetide) – Non-Hematopoietic EPO-Derived Research Peptide
ARA-290, also known as Cibinetide, is a synthetic 11-amino acid peptide derived from the helix B surface domain of erythropoietin (EPO) . Unlike full-length EPO, ARA-290 is non-erythropoietic—it does not stimulate red blood cell production—but retains potent tissue-protective and anti-inflammatory properties through selective activation of the Innate Repair Receptor (IRR) . This targeted mechanism makes ARA-290 a compelling research tool for investigating neuropathy, metabolic disorders, and inflammation-driven tissue damage. This research-grade peptide is strictly for laboratory investigation and is not intended for human consumption.
Key Factual Details
| Attribute | Detail |
|---|---|
| Chemical Name | ARA-290 (Cibinetide) |
| Synonyms | ARA 290, PH-BSP, Cibinetide |
| Sequence | {Glp}-Glu-Gln-Leu-Glu-Arg-Ala-Leu-Asn-Ser-Ser ({pGlu}-EQLERALNSS) |
| Molecular Formula | C₅₁H₈₄N₁₆O₂₁ |
| Molecular Weight | ~1,257.31 g/mol |
| CAS Number | 1208243-50-8 |
| Purity | ≥98% (HPLC verified) |
| Classification | Non-erythropoietic EPO analog / Innate Repair Receptor agonist |
Mechanism of Action & Research Applications
Selective Innate Repair Receptor (IRR) Activation: ARA-290 binds to the heterodimeric IRR composed of the erythropoietin receptor (EPOR) and the β-common receptor (CD131), which is upregulated in tissues under stress, inflammation, or metabolic insult . This initiates a cascade of pro-survival and anti-inflammatory signaling through the JAK2/STAT, PI3K/Akt pathways, and inhibits the NF-κB inflammatory pathway .
Research Applications:
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Neuropathy & Nerve Regeneration: Preclinical and clinical data demonstrate improvements in corneal nerve fiber density (CNFD) and reductions in neuropathic pain scores
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Cardiovascular Aging: Reduces cardiac inflammation, preserves left ventricular ejection fraction, and ameliorates frailty in aged models
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Diabetic Research: Improves glucose tolerance and insulin release in type 2 diabetic models
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Inflammatory Disorders: Suppresses pro-inflammatory cytokines via NF-κB inhibition
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Anti-Apoptotic Studies: Enhances cell survival and reduces apoptosis in stressed tissues
Research Parameters
All dosages are for in-vitro and preclinical research use only and are not intended for human consumption.
Preclinical Rodent Dosing :
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Typical Dose: 30-70 µg/kg body weight
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Route: Subcutaneous (SC) or intraperitoneal (IP) injection
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Frequency: Once daily
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Study Duration: 4-28 days or chronic (15-month) protocols
Clinical Research Dosing (Published Data) :
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Standard Dose: 2-4 mg daily
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Route: Subcutaneous (SC) injection
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Protocol: 28-day continuous daily dosing
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Cycle: 4 weeks on, followed by 8-12 weeks off before another cycle
Storage:
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Store lyophilized powder at -20°C
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Protect from light and moisture











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