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Triacetyl resveratrol

Cat. No. M8211
Triacetyl resveratrol Structure
Size Price Availability Quantity
100mg USD 45  USD45 In stock
500mg USD 70  USD70 In stock
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Quality Control & Documentation
Biological Activity

Triacetyl resveratrol displays superior bioavailability to the parent compound, resveratrol. The compound induces p53 activity and inhibits proliferation in breast and prostate tumor cell lines.

Chemical Information
Molecular Weight 354.35
Formula C20H18O6
CAS Number 42206-94-0
Form Solid
Solubility (25°C) DMSO: ≥18 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
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] Kaibo Guo, et al. Resveratrol and Its Analogs: Potent Agents to Reverse Epithelial-to-Mesenchymal Transition in Tumors

[2] Junsheng Fu, et al. Triacetyl resveratrol upregulates miRNA‑200 and suppresses the Shh pathway in pancreatic cancer: A potential therapeutic agent

[3] Jiaa Park, et al. Effects of resveratrol, oxyresveratrol, and their acetylated derivatives on cellular melanogenesis

[4] Tze-Chen Hsieh, et al. Regulation of p53 and cell proliferation by resveratrol and its derivatives in breast cancer cells: an in silico and biochemical approach targeting integrin αvβ3

[5] Maria Grazia Sarpietro, et al. Interaction of resveratrol and its trimethyl and triacetyl derivatives with biomembrane models studied by differential scanning calorimetry

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