ARA-290 (Cibinetide) Peptide

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Description

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:

  • Neuropathy & Nerve Regeneration: Preclinical and clinical data demonstrate improvements in corneal nerve fiber density (CNFD) and reductions in neuropathic pain scores 

  • Cardiovascular Aging: Reduces cardiac inflammation, preserves left ventricular ejection fraction, and ameliorates frailty in aged models 

  • Diabetic Research: Improves glucose tolerance and insulin release in type 2 diabetic models 

  • Inflammatory Disorders: Suppresses pro-inflammatory cytokines via NF-κB inhibition 

  • 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 :

  • Typical Dose: 30-70 µg/kg body weight

  • Route: Subcutaneous (SC) or intraperitoneal (IP) injection

  • Frequency: Once daily

  • Study Duration: 4-28 days or chronic (15-month) protocols

Clinical Research Dosing (Published Data) :

  • Standard Dose: 2-4 mg daily

  • Route: Subcutaneous (SC) injection

  • Protocol: 28-day continuous daily dosing

  • Cycle: 4 weeks on, followed by 8-12 weeks off before another cycle 

Storage:

  • Store lyophilized powder at -20°C

  • Protect from light and moisture

Additional information

Quantity

5mg*10vials, 10mg*10vials, 16mg*10vials

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