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Farglitazar

Cat. No. M29067
Farglitazar Structure
Synonym:

GI262570; GI262570X

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Quality Control & Documentation
Biological Activity

Farglitazar is a PPARγ agonist that has significant therapeutic benefits such as glycemic control in type 2 diabetic patients.

Chemical Information
Molecular Weight 546.61
Formula C34H30N2O5
CAS Number 196808-45-4
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
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] Dan W Reynolds, et al. J Pharm Sci. The Degradation Chemistry of Farglitazar and Elucidation of the Oxidative Degradation Mechanisms

[2] John McHutchison, et al. Gastroenterology. Farglitazar lacks antifibrotic activity in patients with chronic hepatitis C infection

[3] A Tomillero, et al. Methods Find Exp Clin Pharmacol. Gateways to clinical trials

[4] Colin Spraggs, et al. Pharmacogenet Genomics. Genetic variants in the epithelial sodium channel associate with oedema in type 2 diabetic patients receiving the peroxisome proliferator-activated receptor gamma agonist farglitazar

[5] Alexander Tenenbaum, et al. Cardiovasc Diabetol. Dual and pan-peroxisome proliferator-activated receptors (PPAR) co-agonism: the bezafibrate lessons

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  Catalog
Abmole Inhibitor Catalog




Keywords: Farglitazar, GI262570; GI262570X supplier, PPAR, inhibitors, activators


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