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β-Funaltrexamine (β-FNA) is a selective, irreversible antagonist of the μ opioid receptor (μopioid receptor) with anti-inflammatory and neuroprotective properties. It reduces TLR4 signaling, inhibits cytokine-induced iNOS activation and neuroinflammation, and improves neuronal degeneration. Additionally, β-Funaltrexamine suppresses NF-κB signaling and chemokine expression in human astrocytes and mice. This compound is utilized in research for neurodegenerative diseases, such as stroke.
| 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 | β-Funaltrexamine (β-FNA) is a selective, irreversible antagonist of the μ opioid receptor (μopioid receptor) with anti-inflammatory and neuroprotective properties. It reduces TLR4 signaling, inhibits cytokine-induced iNOS activation and neuroinflammation, and improves neuronal degeneration. Additionally, β-Funaltrexamine suppresses NF-κB signaling and chemokine expression in human astrocytes and mice. This compound is utilized in research for neurodegenerative diseases, such as stroke. |
| Synonyms | β-FNA |
| Molecular Weight | 454.52 |
| Formula | C25H30N2O6 |
| Cas No. | 72782-05-9 |
| Smiles | O[C@]12[C@@]34C=5C(O[C@]3([C@H](NC(/C=C/C(OC)=O)=O)CC1)[H])=C(O)C=CC5C[C@]2(N(CC6CC6)CC4)[H] |
| 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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