N-(3-(Imidazo[1,2-a]pyridin-2-yl)phenyl)-8-methoxy-2-oxo-2H-chromene-3-carboxamide
98%
- Product Code: 53532
CAS:
1100353-03-4
| Molecular Weight: | 411.4095 g./mol | Molecular Formula: | C₂₄H₁₇N₃O₄ |
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| EC Number: | MDL Number: | MFCD12020897 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development due to its potential biological activities. It is often studied for its role as a kinase inhibitor, which makes it a candidate for targeting various types of cancers. The structure of the compound, featuring an imidazo[1,2-a]pyridine moiety, is particularly significant in enhancing its binding affinity to specific protein kinases involved in cell signaling pathways. Researchers are exploring its efficacy in inhibiting tumor growth and metastasis, making it a promising lead compound for anticancer therapies. Additionally, its chromene component contributes to its potential antioxidant properties, which could be beneficial in reducing oxidative stress-related damage in cells. Ongoing studies aim to optimize its pharmacokinetic properties and evaluate its therapeutic potential in preclinical models.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | $235.06 |
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| 0.005 | 10-20 days | $271.22 |
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| 0.025 | 10-20 days | $356.20 |
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| 0.100 | 10-20 days | $1,301.86 |
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N-(3-(Imidazo[1,2-a]pyridin-2-yl)phenyl)-8-methoxy-2-oxo-2H-chromene-3-carboxamide
This compound is primarily utilized in the field of medicinal chemistry and drug development due to its potential biological activities. It is often studied for its role as a kinase inhibitor, which makes it a candidate for targeting various types of cancers. The structure of the compound, featuring an imidazo[1,2-a]pyridine moiety, is particularly significant in enhancing its binding affinity to specific protein kinases involved in cell signaling pathways. Researchers are exploring its efficacy in inhibiting tumor growth and metastasis, making it a promising lead compound for anticancer therapies. Additionally, its chromene component contributes to its potential antioxidant properties, which could be beneficial in reducing oxidative stress-related damage in cells. Ongoing studies aim to optimize its pharmacokinetic properties and evaluate its therapeutic potential in preclinical models.
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