(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%

Reagent Code: #126297
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CAS Number 924641-59-8

science Other reagents with same CAS 924641-59-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 437.51 g/mol
Formula C23H28FN7O
badge Registry Numbers
MDL Number MFCD13184818
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, dry and sealed

description 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.

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Size Availability Unit Price Quantity
inventory 5mg
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
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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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