Drug intelligence / Profile preview

licochalcone E

Development stage
Preclinical
Lead developer
Hallym University
Modality
Small Molecules
Administration
Intraperitoneal, Oral
01

Overview

Licochalcone E is a natural retrochalcone flavonoid isolated from the roots of Glycyrrhiza species (licorice), such as Glycyrrhiza inflata and Glycyrrhiza uralensis. It exhibits a wide range of pharmacological properties, including anti-inflammatory, anti-cancer, anti-diabetic, and anti-obesity activities. Mechanistically, licochalcone E acts as a partial agonist of peroxisome proliferator-activated receptor gamma (PPARγ) and an agonist of liver X receptor beta (LXRβ), while antagonizing liver X receptor alpha (LXRα). It also activates the Nrf2/ARE antioxidant pathway and inhibits the activation of NF-κB and AP-1 by suppressing AKT and MAPK signaling pathways. In preclinical models, licochalcone E has demonstrated the ability to inhibit solid tumor growth and metastasis in breast cancer, improve insulin sensitivity, and ameliorate hepatic steatosis.

Other names
Lico-Elico E
02

Targets

NFE2L2 (Nuclear factor (erythroid-derived 2)-like 2)LXR-beta (Oxysterols receptor LXR-beta)LXR-alpha (Oxysterols receptor LXR-alpha)PPARG (Peroxisome proliferator-activated receptor gamma)

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