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Harpagoside

Cat. No. M4284
Harpagoside Structure
Size Price Availability Quantity
5mg USD 65  USD65 In stock
10mg USD 100  USD100 In stock
20mg USD 160  USD160 In stock
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Quality Control & Documentation
Biological Activity

Harpagoside was separated from Harpagophytum procumbens (Hp). Harpagoside inhibited COX-1 and COX-2 activity and NO production.

Chemical Information
Molecular Weight 494.49
Formula C24H30O11
CAS Number 19210-12-9
Solubility (25°C) DMSO ≥ 60 mg/mL
Storage 4°C, protect from light, dry, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Yun Wei Lu, et al. The protective effect of harpagoside on angiotensin II (Ang II)-induced blood-brain barrier leakage in vitro

[2] Luigi Menghini, et al. Devil's claw (Harpagophytum procumbens) and chronic inflammatory diseases: A concise overview on preclinical and clinical data

[3] Chen Chen, et al. Harpagoside Rescues the Memory Impairments in Chronic Cerebral Hypoperfusion Rats by Inhibiting PTEN Activity

[4] Abdul Haseeb, et al. Harpagoside suppresses IL-6 expression in primary human osteoarthritis chondrocytes

[5] Milen I Georgiev, et al. Harpagoside: from Kalahari Desert to pharmacy shelf

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Keywords: Harpagoside supplier, COX, inhibitors, activators


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