Drug intelligence / Profile preview

xanthoangelol

Development stage
Preclinical
Lead developer
Hormel Institute
Modality
Small Molecules
Administration
Oral
01

Overview

Xanthoangelol is a bioactive chalcone primarily isolated from the Ashitaba plant (*Angelica keiskei*). It has been extensively studied for its diverse pharmacological properties, including anti-tumor, anti-inflammatory, and anti-diabetic activities. In the context of oncology, xanthoangelol acts as a dual inhibitor of the BRAF and PI3-K signaling pathways, which are frequently dysregulated in various cancers, particularly melanoma. By targeting these kinases, xanthoangelol suppresses downstream signaling, leading to G1 phase cell cycle arrest and the induction of apoptosis. Preclinical research has demonstrated that xanthoangelol can significantly reduce tumor incidence and volume in BRAF-activated and Pten-deficient melanoma models, suggesting its potential as a chemopreventive or therapeutic agent.

Other names
xanthoangelol A
02

Targets

PI3K (Phosphoinositide-3-kinase regulatory subunit 6)BRAF (B-Raf proto-oncogene, serine/threonine kinase)

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