(S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone
97%
- Product Code: 126297
CAS:
924641-59-8
| Molecular Weight: | 437.51 g./mol | Molecular Formula: | C23H28FN7O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13184818 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, dry and sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as a targeted therapeutic agent. It is designed to inhibit specific protein kinases involved in signaling pathways that drive the growth and survival of cancer cells. By selectively binding to these kinases, it disrupts their activity, thereby halting the proliferation of malignant cells and inducing apoptosis. This makes it a promising candidate for the treatment of various cancers, especially those driven by mutations or overexpression of the targeted kinases. Additionally, its structure is optimized for enhanced bioavailability and reduced off-target effects, which is critical for minimizing adverse reactions in patients. Research is ongoing to explore its efficacy in preclinical and clinical settings, with potential applications in personalized medicine based on genetic profiles of tumors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿25,940.00 |
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(S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as a targeted therapeutic agent. It is designed to inhibit specific protein kinases involved in signaling pathways that drive the growth and survival of cancer cells. By selectively binding to these kinases, it disrupts their activity, thereby halting the proliferation of malignant cells and inducing apoptosis. This makes it a promising candidate for the treatment of various cancers, especially those driven by mutations or overexpression of the targeted kinases. Additionally, its structure is optimized for enhanced bioavailability and reduced off-target effects, which is critical for minimizing adverse reactions in patients. Research is ongoing to explore its efficacy in preclinical and clinical settings, with potential applications in personalized medicine based on genetic profiles of tumors.
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