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AGU661 is an inhibitor of microsomal prostaglandin E2 synthase-1 (mPGES-1) with an IC50 of 0.22 nM. It effectively reduces PGE2 production in human pro-inflammatory M1 macrophages and activated monocytes without affecting other lipid mediator pathways. Despite its poor physicochemical properties, low metabolic stability, and high plasma protein binding rate, encapsulating AGU661 in PLGA-based nanoparticles significantly enhances its bioactivity. AGU661 is applicable for research on inflammatory diseases.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | AGU661 is an inhibitor of microsomal prostaglandin E2 synthase-1 (mPGES-1) with an IC50 of 0.22 nM. It effectively reduces PGE2 production in human pro-inflammatory M1 macrophages and activated monocytes without affecting other lipid mediator pathways. Despite its poor physicochemical properties, low metabolic stability, and high plasma protein binding rate, encapsulating AGU661 in PLGA-based nanoparticles significantly enhances its bioactivity. AGU661 is applicable for research on inflammatory diseases. |
| Molecular Weight | 594.94 |
| Formula | C28H21ClF6N4O2 |
| Cas No. | 3038861-75-2 |
| Smiles | O=C(NC=1C=CC(=CC1)C2=NC3=CC=C(C=C3N2)C(F)(F)F)C4=CC(=CC=C4Cl)CNC(=O)C5(CCC5)C(F)(F)F |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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