Drug intelligence / Profile preview

P1-1

Development stage
Preclinical
Lead developer
Shenzhen Turier Biotech
Modality
Cyclic Peptides → Modified Peptides → Peptides
01

Overview

P1-1 is a preclinical cyclic peptide antagonist targeting G protein-coupled receptor 55 (GPR55), developed by Shenzhen Turier Biotech for the treatment of liver fibrosis and liver inflammation. The drug functions by suppressing collagen secretion in hepatic stellate cells and reducing the production of reactive oxygen species (ROS). It also attenuates endoplasmic reticulum (ER) stress and inhibits mitochondria-associated hepatocyte apoptosis. Preclinical animal models, including CCl4-induced and MCD-diet-induced models, have shown that P1-1 effectively ameliorates acute liver inflammation and fibrosis, representing a novel approach to treating these conditions via GPR55 antagonism.

02

Targets

GPR55 (G protein-coupled receptor 55)

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