Drug intelligence / Profile preview

antroquinonol

Development stage
Phase 2
Lead developer
Golden Biotechnology
Modality
Small Molecules
Administration
Oral, Topical
01

Overview

Antroquinonol is a small molecule natural product isolated from the fungus Antrodia camphorata (also known as Taiwanofungus camphoratus). It has been investigated primarily for its anticancer, anti-inflammatory, and antihyperlipidemic properties. Mechanistically, antroquinonol acts as an inhibitor of protein isoprenyl transferases (including farnesyltransferase and geranylgeranyltransferase-I), leading to inhibition of Ras and Rho signaling pathways in cancer cells[6]. It also modulates key oncogenic pathways such as PI3K/Akt/mTOR and activates AMP-dependent protein kinase (AMPK), resulting in cell cycle arrest, apoptosis (both caspase-dependent and -independent), autophagic cell death, and senescence[3][8]. Additional reported mechanisms include modulation of epidermal growth factor receptor (EGFR) signaling and mitogen activated protein kinase pathways[4]. Preclinical studies have shown cytotoxicity against various human cancer cell lines; however, some later studies reported minimal activity in certain models[1]. Clinically, it has reached phase II trials for indications including non-small cell lung cancer, pancreatic cancer, acute myeloid leukemia, hepatitis B infection, atopic dermatitis, colorectal cancer, COVID‑19 pneumonia, and hyperlipidemia[4].

Brand names
Hocena
Other names
antroquinonolAntroquinonol A(+)-Antroquinonol A
02

Targets

AMPK (Adenosine monophosphate–activated protein kinase)GGTase I (Geranylgeranyl transferase type I)FTase (Protein Farnesyltransferase)EGFR (Epidermal growth factor receptor)mTOR (Mammalian target of rapamycin kinase)MEKAKT (RAC-alpha serine/threonine-protein kinase)

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