4-​[8-​amino-​3-​[(2S)​-​1-​(1-​oxo-​2-​butyn-​1-​yl)​-​2-​pyrrolidinyl]​imidazo[1,​5-​a]​pyrazin-​1-​yl]​-​N-​2-​pyridinyl-Benzamide

98%

Reagent Code: #234799
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CAS Number 1420477-60-6

science Other reagents with same CAS 1420477-60-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 465.51 g/mol
Formula C₂₆H₂₃N₇O₂
inventory_2 Storage & Handling
Storage 2~8℃, dry

description Product Description

Used in pharmaceutical research as a potent and selective inhibitor of anaplastic lymphoma kinase (ALK). It shows high efficacy in targeting ALK-driven cancers, particularly non-small cell lung cancer (NSCLC) with ALK gene rearrangements. The compound demonstrates strong central nervous system penetration, making it effective against brain metastases commonly associated with advanced NSCLC. Its design allows for improved binding affinity and resistance profile compared to earlier generation inhibitors, supporting its use in both treatment-naïve and resistant cases. Currently investigated in clinical trials for oncology applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,460.00
inventory 250mg
10-20 days ฿5,880.00
inventory 1g
10-20 days ฿15,840.00
inventory 5g
10-20 days ฿48,500.00

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4-​[8-​amino-​3-​[(2S)​-​1-​(1-​oxo-​2-​butyn-​1-​yl)​-​2-​pyrrolidinyl]​imidazo[1,​5-​a]​pyrazin-​1-​yl]​-​N-​2-​pyridinyl-Benzamide
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Used in pharmaceutical research as a potent and selective inhibitor of anaplastic lymphoma kinase (ALK). It shows high efficacy in targeting ALK-driven cancers, particularly non-small cell lung cancer (NSCLC) with ALK gene rearrangements. The compound demonstrates strong central nervous system penetration, making it effective against brain metastases commonly associated with advanced NSCLC. Its design allows for improved binding affinity and resistance profile compared to earlier generation inhibitors, s

Used in pharmaceutical research as a potent and selective inhibitor of anaplastic lymphoma kinase (ALK). It shows high efficacy in targeting ALK-driven cancers, particularly non-small cell lung cancer (NSCLC) with ALK gene rearrangements. The compound demonstrates strong central nervous system penetration, making it effective against brain metastases commonly associated with advanced NSCLC. Its design allows for improved binding affinity and resistance profile compared to earlier generation inhibitors, supporting its use in both treatment-naïve and resistant cases. Currently investigated in clinical trials for oncology applications.

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