Drug intelligence / Profile preview

schisanhenol

Development stage
Preclinical
Lead developer
Shandong First Medical University
Modality
Small Molecules
Administration
Oral, Intraperitoneal (in Preclinical Research), Not Approved For Clinical Use In Humans
01

Overview

Schisanhenol is a natural biphenylcyclooctene-type lignan compound isolated from several Schisandra species, most notably Schisandra chinensis and Schisandra rubriflora[1][4][8][13]. It is being investigated for its **anti-inflammatory**, **antioxidant**, **neuroprotective**, and **hepatoprotective** properties. Mechanistically, schisanhenol inhibits the nuclear factor-kappa B (NF-κB) signaling pathway, suppressing inflammatory cytokine production including TNF-α, IL-6, and IL-1β in both cellular and animal models[1][3][7][12]. It activates SIRT1-PGC-1α signaling and inhibits phosphorylation of Tau, thus demonstrating **potential benefit in cognitive disorders such as Alzheimer's disease**[4]. In models of non-alcoholic fatty liver disease (NAFLD), schisanhenol downregulates miR-802, thereby activating the AMPK pathway and improving hepatic steatosis[10]. It shows promise as a candidate for treating conditions involving cytokine storm, NAFLD, and neurodegeneration. Additionally, it has reported central inhibitory and anticonvulsant actions, making it of potential interest in neurological indications[2][4]. Schisanhenol is commonly used as a research compound in preclinical models, but is not currently approved as a pharmaceutical.

Other names
Gomisin K3Schisanhenol-RMSchisanhenol (Schizanhenol)Schisanhenol/(+)-Gomisin K3Schisandra chinensis phenol(+)-Gomisin K369363-14-0
02

Targets

MMP9 (Matrix metalloproteinase-9)mTOR (Mammalian target of rapamycin kinase)

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