(3-((2-Methylindolin-1-yl)sulfonyl)phenyl)(4-(pyrimidin-2-yl)piperazin-1-yl)methanone

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Reagent Code: #131478
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CAS Number 749868-66-4

science Other reagents with same CAS 749868-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 463.55 g/mol
Formula C₂₄H₂₅N₅O₃S
thermostat Physical Properties
Boiling Point 705.0±70.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.348±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate for kinase inhibitors, particularly in the development of targeted cancer therapies. Shows activity in modulating signaling pathways involved in tumor growth and proliferation. Investigated for potential use in treating hematological malignancies and solid tumors due to its ability to selectively inhibit specific tyrosine kinases. Also employed in structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,890.00
inventory 250mg
10-20 days ฿38,890.00

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(3-((2-Methylindolin-1-yl)sulfonyl)phenyl)(4-(pyrimidin-2-yl)piperazin-1-yl)methanone
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Used in pharmaceutical research as a key intermediate for kinase inhibitors, particularly in the development of targeted cancer therapies. Shows activity in modulating signaling pathways involved in tumor growth and proliferation. Investigated for potential use in treating hematological malignancies and solid tumors due to its ability to selectively inhibit specific tyrosine kinases. Also employed in structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and metabo

Used in pharmaceutical research as a key intermediate for kinase inhibitors, particularly in the development of targeted cancer therapies. Shows activity in modulating signaling pathways involved in tumor growth and proliferation. Investigated for potential use in treating hematological malignancies and solid tumors due to its ability to selectively inhibit specific tyrosine kinases. Also employed in structure-activity relationship (SAR) studies to optimize drug candidates for improved potency and metabolic stability.

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