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MF498

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Catalog No. T16069Cas No. 915191-42-3

MF498 is a novel and selective E prostanoid receptor 4 (EP4 receptor) antagonist, displayed a strong binding affinity for the EP4 receptor (Ki: 0.7 nM).

MF498

MF498

😃Good
Catalog No. T16069Cas No. 915191-42-3
MF498 is a novel and selective E prostanoid receptor 4 (EP4 receptor) antagonist, displayed a strong binding affinity for the EP4 receptor (Ki: 0.7 nM).
Pack SizePriceAvailabilityQuantity
1 mg$17035 days
5 mg$75535 days
10 mg$1,33035 days
25 mg$2,92035 days
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Product Introduction

Bioactivity
Description
MF498 is a novel and selective E prostanoid receptor 4 (EP4 receptor) antagonist, displayed a strong binding affinity for the EP4 receptor (Ki: 0.7 nM).
In vitro
MF498 inhibits PGE2-stimulated cAMP accumulation in a dose-dependent manner (IC50: 1.7 and 17 nM in the absence and presence of 10% serum, respectively). MF498 also displays a relatively good selectivity over other prostanoid receptors, does not compromise the mucosal integrity in the gastrointestinal tract.
In vivo
MF498 on inflammation in adjuvant-caused arthritis (AIA), a rat model for rheumatoid arthritis (RA), and joint pain in a guinea pig model of iodoacetate-induced osteoarthritis (OA). MF498 relieves joint inflammation and pain in rodent models of rheumatoid and osteoarthritis.
Chemical Properties
Molecular Weight603.69
FormulaC32H33N3O7S
Cas No.915191-42-3
Relative Density.1.324 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 31 mg/mL (51.35 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6565 mL8.2824 mL16.5648 mL82.8240 mL
5 mM0.3313 mL1.6565 mL3.3130 mL16.5648 mL
10 mM0.1656 mL0.8282 mL1.6565 mL8.2824 mL
20 mM0.0828 mL0.4141 mL0.8282 mL4.1412 mL
50 mM0.0331 mL0.1656 mL0.3313 mL1.6565 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
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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