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Ciglitazone

Cat. No. M6602
Ciglitazone Structure
Synonym:

ADD-3878; U-63287

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10mg USD 400  USD400 1-2 Weeks
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Quality Control & Documentation
Biological Activity

Ciglitazone is an effective selective PPARγ agonist (EC50=3 μM). Ciglitazone inhibited the proliferation and differentiation of TH17 cells. Ciglitazone is an oral hypoglycemic agent that has been shown to be active in obese hyperglycemic animal models. Ciglitazone induces apoptosis in opossum renal epithelial cells and simultaneously activates nuclear translocation of P38 MAPK and apoptosis-inducing factor (AIF).

Chemical Information
Molecular Weight 333.44
Formula C18H23NO3S
CAS Number 74772-77-3
Solubility (25°C) 1eq. NaOH 33.34 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
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] Wood, et al. Bioorg Med Chem Lett. Discovery and in vitro evaluation of potent TrkA kinase inhibitors: oxindole and aza-oxindoles.

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  Catalog
Abmole Inhibitor Catalog




Keywords: Ciglitazone, ADD-3878; U-63287 supplier, PPAR, inhibitors, activators


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