1-(7-Methoxyquinolin-4-yl)-3-[6-(trifluoromethyl)pyridin-2-yl]urea
98%
- Product Code: 79983
CAS:
1384424-80-9
| Molecular Weight: | 362.31 g./mol | Molecular Formula: | C₁₇H₁₃F₃N₄O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, particularly in the development of kinase inhibitors. It serves as a key intermediate in the synthesis of small molecule drugs targeting various kinases, which are enzymes involved in critical cellular processes such as signaling, growth, and apoptosis. Its structure, featuring a methoxyquinoline and trifluoromethylpyridine moiety, is designed to enhance binding affinity and selectivity towards specific kinase targets. This makes it valuable in research focused on treating diseases like cancer, inflammatory disorders, and autoimmune conditions. Additionally, its urea linkage contributes to its stability and ability to interact with biological targets, further supporting its role in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿6,291.00 |
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| 0.050 | 10-20 days | ฿23,391.00 |
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1-(7-Methoxyquinolin-4-yl)-3-[6-(trifluoromethyl)pyridin-2-yl]urea
This compound is primarily utilized in the field of medicinal chemistry, particularly in the development of kinase inhibitors. It serves as a key intermediate in the synthesis of small molecule drugs targeting various kinases, which are enzymes involved in critical cellular processes such as signaling, growth, and apoptosis. Its structure, featuring a methoxyquinoline and trifluoromethylpyridine moiety, is designed to enhance binding affinity and selectivity towards specific kinase targets. This makes it valuable in research focused on treating diseases like cancer, inflammatory disorders, and autoimmune conditions. Additionally, its urea linkage contributes to its stability and ability to interact with biological targets, further supporting its role in drug discovery and development.
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