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PSN632408

Catalog No. T16678Cas No. 857652-30-3

PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).

PSN632408

PSN632408

Catalog No. T16678Cas No. 857652-30-3
PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).
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Product Introduction

Bioactivity
Description
PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).
In vitro
GPR119 (previously designated SNORF25) is an orphan G protein-coupled receptor expressed predominantly in the pancreas and gastrointestinal tract in humans and in the brain, pancreas, and gastrointestinal tract in rodents. GPR119 agonist Systemic administration of PSN632408 (30 mg/kgintraperitoneally) inhibits food intake, reduces weight gain, and white adipose tissue deposition in rats. It mediates a reduction in food intake and body weight gain in rats upon treatment with oleoyl ethanolamide (OEA), an endogenous, potent agonist for PPARα. These data suggest that PSN632408 may be useful as a therapeutic agent for the treatment of obesity.
Chemical Properties
Molecular Weight360.41
FormulaC18H24N4O4
Cas No.857652-30-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (138.73 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7746 mL13.8731 mL27.7462 mL138.7309 mL
5 mM0.5549 mL2.7746 mL5.5492 mL27.7462 mL
10 mM0.2775 mL1.3873 mL2.7746 mL13.8731 mL
20 mM0.1387 mL0.6937 mL1.3873 mL6.9365 mL
50 mM0.0555 mL0.2775 mL0.5549 mL2.7746 mL
100 mM0.0277 mL0.1387 mL0.2775 mL1.3873 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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