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Mechanism of Action

Activates Nrf2/HO-1 antioxidant response element pathway, suppresses NF-κB and MAPK pro-inflammatory signalling cascades, inhibits CYP2E1-mediated hepatotoxic bioactivation, enhances superoxide dismutase and catalase activity, and inhibits α-glucosidase and α-amylase for glycaemic modulation.
Inhibits NF-κB signalling and COX-2 expression; scavenges reactive oxygen species; upregulates hepatic antioxidant enzymes (SOD, CAT, GST); modulates Nrf2 pathway.

Research Notes

Extensive preclinical evidence in rodent models shows kolaviron protects against carbon tetrachloride-, alcohol-, and aflatoxin-induced hepatotoxicity; reduces fasting blood glucose comparably to glibenclamide in diabetic models; and demonstrates broad-spectrum antimicrobial and anti-inflammatory activity. Phase I human safety data from Nigerian academic centres indicate tolerability; Phase II efficacy trials in hepatic and diabetic endpoints are ongoing as of 2024.

Multiple rodent studies demonstrate hepatoprotective activity against carbon tetrachloride and acetaminophen-induced liver injury. Anti-inflammatory and antidiabetic effects have been documented in vitro and in vivo, though human clinical trials remain limited.

Found In 2 Herbs

3D Molecular Structure

Biflavonoid complex (GB1 + GB2 + kolaflavanone)
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Kolaviron

Biflavonoid complex (GB1 + GB2 + kolaflavanone)Polyphenolic antioxidants protecting cells from oxidative damage

Representative pattern: C₁₅H₁₀O₃

Atoms
Carbon
Oxygen

Live Research

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