1,2,3,4-tetrahydro-3-(1H-indol-3-yl)-2-(2-methoxyethyl)-N-(2-methoxy-5-methylphenyl)-1-oxo-, (3R,4R)-rel-4-Isoquinolinecarboxamide

98%

Reagent Code: #245672
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CAS Number 943934-76-7

science Other reagents with same CAS 943934-76-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 483.56 g/mol
Formula C₂₉H₂₉N₃O₄
thermostat Physical Properties
Boiling Point 710.7±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.273±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical research as a potent and selective inhibitor of specific kinases involved in cellular signaling pathways. Shows promise in the development of targeted cancer therapies, particularly for tumors driven by dysregulated kinase activity. Demonstrates high permeability across cell membranes and favorable metabolic stability, making it suitable for in vivo studies. Also employed in neuroscience research due to its structural similarity to indole alkaloids, potentially influencing neuroprotective mechanisms. Its stereochemistry enhances binding affinity and specificity, reducing off-target effects in experimental models.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿39,590.00
inventory 5mg
10-20 days ฿10,990.00

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1,2,3,4-tetrahydro-3-(1H-indol-3-yl)-2-(2-methoxyethyl)-N-(2-methoxy-5-methylphenyl)-1-oxo-, (3R,4R)-rel-4-Isoquinolinecarboxamide
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Used in pharmaceutical research as a potent and selective inhibitor of specific kinases involved in cellular signaling pathways. Shows promise in the development of targeted cancer therapies, particularly for tumors driven by dysregulated kinase activity. Demonstrates high permeability across cell membranes and favorable metabolic stability, making it suitable for in vivo studies. Also employed in neuroscience research due to its structural similarity to indole alkaloids, potentially influencing neuropro

Used in pharmaceutical research as a potent and selective inhibitor of specific kinases involved in cellular signaling pathways. Shows promise in the development of targeted cancer therapies, particularly for tumors driven by dysregulated kinase activity. Demonstrates high permeability across cell membranes and favorable metabolic stability, making it suitable for in vivo studies. Also employed in neuroscience research due to its structural similarity to indole alkaloids, potentially influencing neuroprotective mechanisms. Its stereochemistry enhances binding affinity and specificity, reducing off-target effects in experimental models.

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