ISOFEBRIFUGINE
≥98%
- Product Code: 200540
CAS:
32434-44-9
| Molecular Weight: | 301.34 g./mol | Molecular Formula: | C₁₆H₁₉N₃O₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 129-130 °C | Boiling Point: | 519.8±58.0 °C(Predicted) |
| Density: | 1.48±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Isofebrifugine is primarily studied for its potent antimalarial properties. It has demonstrated significant activity against Plasmodium falciparum, the parasite responsible for the most severe form of malaria. Its mechanism involves inhibiting protein synthesis in the parasite, which disrupts its growth and replication. Due to its effectiveness at low concentrations, isofebrifugine serves as a lead compound in the development of new antimalarial drugs, especially in response to increasing resistance to existing treatments like chloroquine. Additionally, it has shown potential in anti-inflammatory and anticancer research, with studies indicating it may suppress certain signaling pathways involved in tumor progression. However, its clinical use is limited by toxicity concerns, prompting efforts to synthesize safer derivatives while retaining its biological activity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5mg | 10-20 days | ฿26,880.00 |
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ISOFEBRIFUGINE
Isofebrifugine is primarily studied for its potent antimalarial properties. It has demonstrated significant activity against Plasmodium falciparum, the parasite responsible for the most severe form of malaria. Its mechanism involves inhibiting protein synthesis in the parasite, which disrupts its growth and replication. Due to its effectiveness at low concentrations, isofebrifugine serves as a lead compound in the development of new antimalarial drugs, especially in response to increasing resistance to existing treatments like chloroquine. Additionally, it has shown potential in anti-inflammatory and anticancer research, with studies indicating it may suppress certain signaling pathways involved in tumor progression. However, its clinical use is limited by toxicity concerns, prompting efforts to synthesize safer derivatives while retaining its biological activity.
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