Rosiglitazone HCl is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.
|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 resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 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 resveratrol of 11.2 mg/kg.
|Solubility||79 mg/mL in DMSO|
|Source||The FASEB Journal (2017). Figure 1. Rosiglitazone (Abmole Bioscience, Shanghai, China)|
|Method||3T3-L1 cell differentiation|
|Cell Lines||3T3-L1 cell|
|Incubation Time||3 d|
|Results||FTO is positively regulated by PKCb. Immunoblot analyses were performed with the indicated antibodies. The quantifications of immunoblots came from 3 repeats of the experiments.|
FASEB J. 2017 Jun 16;pii: fj.201601159RR.
Protein kinase Cβ activates fat mass and obesity-associated protein by influencing its ubiquitin/proteasome degradation.
Rosiglitazone HCl purchased from AbMole
Lack of effect of colesevelam HCl on the single-dose pharmacokinetics of aspirin, atenolol, enalapril, phenytoin, rosiglitazone, and sitagliptin.
He L, et al. Diabetes Res Clin Pract. 2014 Jun;104(3):401-9. PMID: 24721587.
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