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The anti-inflammatory agent 41 (13a) markedly inhibits lipopolysaccharide (LPS)-induced expression of the proinflammatory cytokines IL-6 and TNF-α in J774A.1, THP-1, and LX-2 cells, while also preventing the activation of the NF-κB pathway [1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | The anti-inflammatory agent 41 (13a) markedly inhibits lipopolysaccharide (LPS)-induced expression of the proinflammatory cytokines IL-6 and TNF-α in J774A.1, THP-1, and LX-2 cells, while also preventing the activation of the NF-κB pathway [1]. |
| In vitro | Anti-inflammatory agent 41 (13a) significantly reduced LPS-induced nuclear translocation of p65 in J774A.1 macrophages. |
| Molecular Weight | 543.57 |
| Formula | C33H25N3O5 |
| Cas No. | 2896204-90-1 |
| Smiles | C(NC1=CC=C(OC=2C3=C(C=C(OC)C(OC)=C3)N=CC2)C=C1)(=O)C4=CN(C=5C(C4=O)=CC=CC5)C6=CC=CC=C6 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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