2-(4-(4-(aminomethyl)-1-oxo-1,2-dihydrophthalazin-6-yl)-1-methyl-1H-pyrazol-5-yl)-4-chloro-6-cyclopropoxy-3-fluorobenzonitrile

98%

Reagent Code: #196869
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CAS Number 2630904-45-7

science Other reagents with same CAS 2630904-45-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.89 g/mol
Formula C₂₃H₁₈ClFN₆O₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a potent and selective inhibitor of certain kinases involved in inflammatory and oncogenic signaling pathways. Shows promise in preclinical studies for targeted cancer therapy, particularly in tumors driven by dysregulated kinase activity. Its structure allows for high binding affinity and improved metabolic stability, making it a candidate for oral drug formulations. Also investigated for modulating immune responses in autoimmune diseases due to its ability to cross cell membranes efficiently and exert intracellular effects at low concentrations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿21,770.00
inventory 100mg
10-20 days ฿62,820.00
inventory 250mg
10-20 days ฿106,770.00

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2-(4-(4-(aminomethyl)-1-oxo-1,2-dihydrophthalazin-6-yl)-1-methyl-1H-pyrazol-5-yl)-4-chloro-6-cyclopropoxy-3-fluorobenzonitrile
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Used in pharmaceutical research as a potent and selective inhibitor of certain kinases involved in inflammatory and oncogenic signaling pathways. Shows promise in preclinical studies for targeted cancer therapy, particularly in tumors driven by dysregulated kinase activity. Its structure allows for high binding affinity and improved metabolic stability, making it a candidate for oral drug formulations. Also investigated for modulating immune responses in autoimmune diseases due to its ability to cross ce

Used in pharmaceutical research as a potent and selective inhibitor of certain kinases involved in inflammatory and oncogenic signaling pathways. Shows promise in preclinical studies for targeted cancer therapy, particularly in tumors driven by dysregulated kinase activity. Its structure allows for high binding affinity and improved metabolic stability, making it a candidate for oral drug formulations. Also investigated for modulating immune responses in autoimmune diseases due to its ability to cross cell membranes efficiently and exert intracellular effects at low concentrations.

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