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Pradefovir mesylate

Cat. No. M14315
Pradefovir mesylate Structure
Synonym:

Remofovir mesylate

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Quality Control & Documentation
Biological Activity

Pradefovir mesylate is a good substrate for liver CYP3A4. Pradefovir is converted to 9-(2-phosphonylmethoxyethyl)adenine (PMEA) in human liver microsomes with a Km of 60 μM.

Chemical Information
Molecular Weight 519.9
CAS Number 625095-61-6
Solubility (25°C) Water 90 mg/mL
Storage 2-8°C, 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] Hong Zhang, et al. Safety, efficacy, and pharmacokinetics of pradefovir for the treatment of chronic hepatitis B infection

[2] Qingqing Xiao, et al. Factors limiting the extent of absolute bioavailability of pradefovir in rat

[3] K Raja Reddy, et al. Pradefovir: a prodrug that targets adefovir to the liver for the treatment of hepatitis B

[4] Chin-chung Lin, et al. Metabolic activation of pradefovir by CYP3A4 and its potential as an inhibitor or inducer

[5] Chin-chung Lin, et al. Pharmacokinetics of pradefovir and PMEA in healthy volunteers after oral dosing of pradefovir

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Keywords: Pradefovir mesylate, Remofovir mesylate supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators


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