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Mechanism of Action

Multitarget anti-inflammatory: inhibits HSP90 (disrupting oncogenic signalling clients), NF-κB, and STAT3 pathways; activates Nrf2/HO-1 antioxidant response; modulates leptin signalling in hypothalamic neurons (anti-obesity mechanism); inhibits mast cell degranulation (anti-allergic). Also demonstrated proteasome inhibitory and pro-apoptotic activity.
NF-κB pathway inhibition; HSP90 inhibition leading to immunoproteasome dysfunction; broad anti-inflammatory action

Research Notes

ChuchuhuasiSouth American

Celastrol has attracted extraordinary research attention — over 1,000 publications as of 2024 — as a multi-target natural compound with potential in cancer, neurodegeneration, obesity, and autoimmune disease. A landmark 2015 Nature paper demonstrated dramatic weight loss in obese mice via leptin sensitisation. Human data are limited to traditional use; pharmacokinetic challenges (poor water solubility, extensive first-pass metabolism) have hampered clinical translation. Significant anti-inflammatory and analgesic effects in animal models of rheumatoid arthritis strongly support chuchuhuasi's traditional anti-rheumatic indication.

Celastrol is a secondary bioactive in thunder god vine with strong anti-inflammatory properties documented in preclinical and clinical studies for autoimmune arthritis. More selective than triptolide for inflammation while showing reduced acute toxicity, though long-term safety requires monitoring.

Found In 2 Herbs

3D Molecular Structure

Quinone methide triterpenoid (pentacyclic)
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Celastrol

Quinone methide triterpenoid (pentacyclic)Modified terpenes with diverse biological activities

Representative pattern: C₁₀H₁₆O

Atoms
Carbon
Oxygen
Hydrogen

Live Research

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