Drug intelligence / Profile preview

etrinabdione

Development stage
Phase 2
Lead developer
Emerald Health Pharmaceuticals
Modality
Small Molecules
Administration
Oral
01

Overview

Etrinabdione (VCE-004.8) is a semi-synthetic cannabidiol (CBD) derivative and aminoquinone compound developed as an orally active small molecule drug. It acts as a dual agonist of peroxisome proliferator-activated receptor gamma (PPARγ) and cannabinoid receptor type 2 (CB2), with additional activity on the hypoxia-inducible factor pathway and B55α/AMPK/Sirtuin 1/eNOS signaling axis[1][3][6]. These mechanisms confer potent anti-inflammatory, antifibrotic, neuroprotective, angiogenic, and vasculoprotective effects. Etrinabdione has demonstrated efficacy in preclinical models of multiple sclerosis, scleroderma/systemic sclerosis, ischemic stroke, critical limb ischemia/peripheral artery disease (PAD), and fibrosis by reducing inflammation and promoting tissue repair[1][4][6]. The oral formulation is known as EHP-101.

Brand names
EHP-101EHP101EHP 101
Other names
VCE-004.8VCE004.8VCE 004.8etrinabdione
02

Targets

CNR2 (Cannabinoid receptor type 2)PP2A (Protein phosphatase 2A)PPARG (Peroxisome proliferator-activated receptor gamma)HIF axis (Hypoxia signaling family)

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