Drug intelligence / Profile preview

puerarin 6''-O-xyloside

Development stage
Preclinical
Modality
Small Molecules
Administration
Oral
01

Overview

Puerarin 6''-O-xyloside (P6OX) is a natural isoflavone glycoside isolated from the roots of *Pueraria lobata* (kudzu root). As a small molecule research chemical, it has demonstrated significant pharmacological potential in preclinical models of cancer, osteoporosis, and metabolic disease. Its antitumor mechanism involves the induction of the mitochondria-mediated apoptosis pathway, characterized by the upregulation of pro-apoptotic proteins such as Bax and caspases (caspase-3, -7, and -9) and the downregulation of the anti-apoptotic protein Bcl-2. Furthermore, it acts as a histone deacetylase (HDAC) inhibitor and a PPARα agonist, the latter of which facilitates fatty acid oxidation to alleviate postmenopausal lipid metabolic disorders. While it is widely used in scientific investigation for its phytoestrogenic and anti-osteoporotic properties, it is not currently approved for human therapeutic use.

Other names
Puerarin 6''-O-beta-D-xylopyranosidePuerarin 6''-xyloside
02

Targets

PPARA (Peroxisome proliferator-activated receptor alpha)KDM6B (Lysine-specific demethylase 6B)

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