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GW1929

Cat. No. M13723
GW1929 Structure
Size Price Availability
5mg USD 92  USD92 4-7 Days
10mg USD 165  USD165 4-7 Days
25mg USD 348  USD348 4-7 Days
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Quality Control & Documentation
Biological Activity

GW1929 is a potent PPAR-γ agonist, with a pKi of 8.84 for human PPAR-γ, and pEC50s of 8.56 and 8.27 for human PPAR-γ and murine PPAR-γ, respectively.

Chemical Information
Molecular Weight 495.57
CAS Number 196808-24-9
Solubility (25°C) DMSO ≥ 35 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] Xiaoli Wang, et al. Am J Transl Res. Effects of GW1929 on uterus, ovary and bone metabolism function in perimenopause rats

[2] Ying Qin, et al. Rapid Commun Mass Spectrom. Characterization of the metabolites of GW1929 in rat by liquid chromatography coupled with electrospray ionization tandem mass spectrometry

[3] Swei Sunny Hahn, et al. Cell Signal. GW1929 inhibits α7 nAChR expression through PPARγ-independent activation of p38 MAPK and inactivation of PI3-K/mTOR: The role of Egr-1

[4] Ravinder K Kaundal, et al. Behav Brain Res. GW1929: a nonthiazolidinedione PPARγ agonist, ameliorates neurological damage in global cerebral ischemic-reperfusion injury through reduction in inflammation and DNA fragmentation

[5] M Amine Bouhlel, et al. Cell Metab. PPARgamma activation primes human monocytes into alternative M2 macrophages with anti-inflammatory properties

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