N-(3-Bromophenyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxamide

98%

Reagent Code: #214881
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CAS Number 333419-97-9

science Other reagents with same CAS 333419-97-9

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Weight 359.17 g/mol
Formula C₁₆H₁₁BrN₂O₃
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. Shows potential in developing anti-tumor agents due to its ability to modulate signaling pathways in oncology studies. Also employed in the design of selective protein inhibitors for inflammatory and neurodegenerative diseases. Its structural features support binding to ATP-binding sites in enzymes, making it valuable in structure-activity relationship (SAR) studies for drug optimization.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿10,760.00
inventory 50mg
10-20 days ฿16,130.00
inventory 100mg
10-20 days ฿24,200.00

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N-(3-Bromophenyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxamide
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. Shows potential in developing anti-tumor agents due to its ability to modulate signaling pathways in oncology studies. Also employed in the design of selective protein inhibitors for inflammatory and neurodegenerative diseases. Its structural features support binding to ATP-binding sites in enzymes, making it valuable in structure-acti

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. Shows potential in developing anti-tumor agents due to its ability to modulate signaling pathways in oncology studies. Also employed in the design of selective protein inhibitors for inflammatory and neurodegenerative diseases. Its structural features support binding to ATP-binding sites in enzymes, making it valuable in structure-activity relationship (SAR) studies for drug optimization.

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