2-pyridin-4-yl-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)quinoline-4-carboxamide

96%

Reagent Code: #245749
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CAS Number 851206-31-0

science Other reagents with same CAS 851206-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.47 g/mol
Formula C₂₂H₁₈N₄OS
inventory_2 Storage & Handling
Density 1.362±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical research as a potent and selective inhibitor of kinases involved in inflammatory and oncogenic signaling pathways. Shows promise in the development of targeted cancer therapies, particularly for tumors driven by dysregulated kinase activity. Also investigated for autoimmune disease treatment due to its ability to modulate immune cell function. Its structure allows for high binding affinity to specific ATP-binding sites in target proteins, enhancing therapeutic precision. Commonly employed in preclinical studies to evaluate pathway inhibition and antiproliferative effects in cell cultures and animal models.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿5,930.00
inventory 10mg
10-20 days ฿9,450.00
inventory 25mg
10-20 days ฿18,690.00

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2-pyridin-4-yl-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)quinoline-4-carboxamide
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Used in pharmaceutical research as a potent and selective inhibitor of kinases involved in inflammatory and oncogenic signaling pathways. Shows promise in the development of targeted cancer therapies, particularly for tumors driven by dysregulated kinase activity. Also investigated for autoimmune disease treatment due to its ability to modulate immune cell function. Its structure allows for high binding affinity to specific ATP-binding sites in target proteins, enhancing therapeutic precision. Commonly e

Used in pharmaceutical research as a potent and selective inhibitor of kinases involved in inflammatory and oncogenic signaling pathways. Shows promise in the development of targeted cancer therapies, particularly for tumors driven by dysregulated kinase activity. Also investigated for autoimmune disease treatment due to its ability to modulate immune cell function. Its structure allows for high binding affinity to specific ATP-binding sites in target proteins, enhancing therapeutic precision. Commonly employed in preclinical studies to evaluate pathway inhibition and antiproliferative effects in cell cultures and animal models.

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