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Antroquinonol

Clinical trial

Mechanism of Action

Antroquinonol inhibits cancer cell proliferation through multiple converging pathways. It activates AMP-activated protein kinase (AMPK) and inhibits the PI3K/Akt/mTOR signaling cascade, blocking protein synthesis and cell cycle progression in tumor cells. It suppresses STAT3 phosphorylation, preventing the transcription of genes involved in proliferation, survival, and angiogenesis. In hepatocellular carcinoma cells, antroquinonol induces autophagy through the CHOP/TRB3/Akt/mTOR pathway and promotes apoptosis via mitochondrial depolarization and caspase-3/9 activation. It also inhibits NF-kB nuclear translocation, reducing expression of anti-apoptotic proteins Bcl-2 and Bcl-xL.

Research Notes

Antroquinonol has demonstrated antiproliferative activity against multiple cancer cell lines in vitro including hepatocellular carcinoma (HepG2, Hep3B), pancreatic cancer, non-small cell lung cancer, and colon cancer. In HCC studies, it enhanced the antitumor activity of sorafenib (standard-of-care HCC drug) through complementary cell cycle modulation. A phase II clinical trial (Golden Biotechnology, Inc.) evaluated antroquinonol capsules (Hocena) in patients with advanced cancer. Animal studies demonstrated significant tumor growth inhibition with favorable safety profiles.

Found In 1 Herb

3D Molecular Structure

Tetrahydro-ubiquinone derivative
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Antroquinonol

Tetrahydro-ubiquinone derivativeBioactive phytochemical with therapeutic properties

Representative pattern: C₄H₂NO

Atoms
Carbon
Oxygen
Nitrogen
Hydrogen

Related Compounds (Tetrahydro-ubiquinone derivative)

Live Research

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These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. This content is for educational purposes only and is not a substitute for professional medical advice.