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An 11-amino-acid peptide derived from the tertiary structure of erythropoietin, designed to selectively engage the innate repair receptor without stimulating erythropoiesis; studied in tissue-protection and neuropathic-pain research.
ARA-290, also known as cibinetide, is a short synthetic peptide of eleven amino acids whose sequence corresponds to a specific region on the surface of the erythropoietin (EPO) molecule. Researchers designed it to reproduce the tissue-protective signaling attributed to EPO while avoiding EPO's effect on red-blood-cell production.
Native EPO signals through two receptor systems: the classical homodimeric EPO receptor that drives erythropoiesis, and a distinct tissue-protective complex sometimes termed the innate repair receptor (a heteromer of the EPO receptor and the beta-common receptor, CD131). ARA-290 was engineered to engage the latter selectively.
The peptide has a verified PubChem record (CID 91810664) and is studied in models of inflammation, neuropathic pain, and tissue injury. It is supplied strictly as a research reagent.
ARA-290 is proposed to bind the innate repair receptor, a heterocomplex of the EPO receptor and the beta-common receptor (CD131). Activation of this receptor in experimental models is associated with anti-inflammatory and cytoprotective signaling, including modulation of pathways that reduce apoptosis and inflammatory cytokine activity in injured tissue.
Because ARA-290 does not activate the homodimeric EPO receptor responsible for erythropoiesis, laboratory studies report that it does not raise red-cell mass, distinguishing its signaling profile from full-length EPO.
These summarize published research for informational purposes only and are not usage directions.
Clinical research has evaluated cibinetide in small-fiber neuropathy; Dahan and colleagues and later trials in patients with sarcoidosis-associated neuropathy reported changes in corneal nerve-fiber and pain measures in controlled study settings (cibinetide/ARA-290 neuropathy trials).
Preclinical work by Brines and Cerami established the concept of tissue-protective EPO derivatives, demonstrating in animal models that ARA-290 signaling reduced markers of tissue injury without stimulating erythropoiesis.
Combinations examined in the research literature. Descriptive only — not a recommendation to combine compounds.
References are being compiled for this entry.