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Pseudoginsenoside-F11

Cat. No. M4064
Pseudoginsenoside-F11 Structure
Synonym:

Ginsenoside A1

Size Price Availability Quantity
20mg USD 180  USD180 In stock
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Quality Control & Documentation
Biological Activity

Pseudoginsenoside F11 (Ginsenoside A1), a component of Panax quinquefolium, can resist the learning and memory impairment induced by scopolamine, morphine and methamphetamine in mice.

Chemical Information
Molecular Weight 786.98
Formula C41H70O14
CAS Number 69884-00-0
Solubility (25°C) 10 mM in DMSO
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] Xiaoxiao Fu, et al. Pseudoginsenoside F11 ameliorates the dysfunction of the autophagy-lysosomal pathway by activating calcineurin-mediated TFEB nuclear translocation in neuron during permanent cerebral ischemia

[2] Yongfeng Gao, et al. Pseudoginsenoside-F11 ameliorates thromboembolic stroke injury in rats by reducing thromboinflammation

[3] Ying Hou, et al. Pseudoginsenoside-F11 promotes functional recovery after transient cerebral ischemia by regulating the microglia/macrophage polarization in rats

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Keywords: Pseudoginsenoside-F11, Ginsenoside A1 supplier, Metabolite/Endogenous Metabolite, inhibitors, activators


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