an agonist of the peroxisome proliferator-activated receptor delta (PPARd) signaling pathway
|Solubility (25°C)||DMSO 2 mg/mL|
Powder -20°C 3 years ; 4°C 2 years
In solvent -80°C 6 months ; -20°C 1 month
|Body Surface Area (m2)||0.007||0.025||0.15||0.05||0.02||0.5|
|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.
 T Nakagawa, et al. Arzneimittelforschung. Pharmacokinetics of the new fluoroquinolone balofloxacin in mice, rats, and dogs
 T Nakagawa, et al. Arzneimittelforschung. Determination of the new fluoroquinolone balofloxacin and its metabolites in biological fluids by high performance liquid chromatography
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