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Mechanism of Action

Inhibits NF-κB signaling, reduces TNF-α and IL-6 production; potentiates anti-inflammatory gene expression
Inhibits NF-κB nuclear translocation, suppresses COX-2 and iNOS transcription, reduces TNF-α and IL-1β production in macrophages; may modulate PPAR-γ to dampen inflammatory gene expression

Research Notes

Harpagoside is the primary bioactive in devil's claw and demonstrates significant anti-inflammatory effects in clinical trials for osteoarthritis and low back pain. Studies show dose-dependent reduction in inflammatory markers and pain scores, with effects comparable to some NSAIDs.

Harpagoside from Scrophularia ningpoensis demonstrates anti-inflammatory potency comparable to ibuprofen in carrageenan paw-edema animal models. In vitro studies show dose-dependent inhibition of NF-κB in LPS-stimulated RAW264.7 macrophages. Limited human clinical data; most evidence from Harpagophytum (devil's claw) extracts containing the same compound.

Found In 2 Herbs

3D Molecular Structure

Iridoid glycoside (monoterpene ester glucoside)
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Harpagoside

Iridoid glycoside (monoterpene ester glucoside)Aromatic plant metabolites with anti-inflammatory properties

Representative pattern: C₁₁H₁₄O₆

Atoms
Carbon
Oxygen

Related Compounds (Iridoid glycoside (monoterpene ester glucoside))

Live Research

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