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KRP-297

Cat. No. M29282
KRP-297 Structure
Synonym:

MK-0767

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Quality Control & Documentation
Biological Activity

KRP-297 is a PPARα and PPARγ agonist potentially for the research of type 2 diabetes and dyslipidemia. KRP-297 restores reduced lipid oxidation, and inhibits of enhanced lipogenesis and triglyceride accumulation in the liver.

Chemical Information
Molecular Weight 438.42
Formula C20H17F3N2O4S
CAS Number 213252-19-8
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] Anna C Calkin, et al. Curr Opin Investig Drugs. MK-767. Kyorin/Banyu/Merck

[2] T Yamanouchi. Nihon Rinsho. [KRP-297, MCC-555]

[3] K Murakami, et al. Metabolism. Amelioration by KRP-297, a new thiazolidinedione, of impaired glucose uptake in skeletal muscle from obese insulin-resistant animals

[4] M Nomura, et al. Bioorg Med Chem Lett. (3-substituted benzyl)thiazolidine-2,4-diones as structurally new antihyperglycemic agents

[5] K Murakami, et al. Diabetes. A novel insulin sensitizer acts as a coligand for peroxisome proliferator-activated receptor-alpha (PPAR-alpha) and PPAR-gamma: effect of PPAR-alpha activation on abnormal lipid metabolism in liver of Zucker fatty rats

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  Catalog
Abmole Inhibitor Catalog




Keywords: KRP-297, MK-0767 supplier, PPAR, inhibitors, activators


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