7-(4-(Methylsulfonyl)phenyl)-N-(2-(m-tolyl)pyridin-4-yl)quinolin-4-amine

98%

Reagent Code: #203507
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CAS Number 2763602-67-9

science Other reagents with same CAS 2763602-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 465.57 g/mol
Formula C₂₈H₂₃N₃O₂S
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a potent inhibitor of JAK3 (Janus kinase 3) in biochemical research, particularly targeting kinases involved in inflammatory and oncogenic signaling pathways. It shows promise in studies related to cancer therapy due to its ability to selectively interfere with protein kinases that drive tumor growth. Commonly employed in in vitro assays to modulate cellular activity and investigate signal transduction mechanisms. Its structure supports high binding affinity, making it valuable in the development of targeted therapeutics. Also utilized in structure-activity relationship (SAR) studies to design more effective kinase inhibitors.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿40,290.00
inventory 25mg
10-20 days ฿68,440.00
inventory 50mg
10-20 days ฿116,340.00
inventory 100mg
10-20 days ฿197,730.00

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7-(4-(Methylsulfonyl)phenyl)-N-(2-(m-tolyl)pyridin-4-yl)quinolin-4-amine
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Used as a potent inhibitor of JAK3 (Janus kinase 3) in biochemical research, particularly targeting kinases involved in inflammatory and oncogenic signaling pathways. It shows promise in studies related to cancer therapy due to its ability to selectively interfere with protein kinases that drive tumor growth. Commonly employed in in vitro assays to modulate cellular activity and investigate signal transduction mechanisms. Its structure supports high binding affinity, making it valuable in the development

Used as a potent inhibitor of JAK3 (Janus kinase 3) in biochemical research, particularly targeting kinases involved in inflammatory and oncogenic signaling pathways. It shows promise in studies related to cancer therapy due to its ability to selectively interfere with protein kinases that drive tumor growth. Commonly employed in in vitro assays to modulate cellular activity and investigate signal transduction mechanisms. Its structure supports high binding affinity, making it valuable in the development of targeted therapeutics. Also utilized in structure-activity relationship (SAR) studies to design more effective kinase inhibitors.

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