2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)pyrimidine-4,5,6-triamine

97%

Reagent Code: #188691
label
Alias Vili watermelon intermediate; Vilisigua intermediate; Vilisigua intermediate; Leosigua intermediate
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CAS Number 1350653-30-3

science Other reagents with same CAS 1350653-30-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.34 g/mol
Formula C₁₇H₁₄F₂N₈
badge Registry Numbers
MDL Number MFCD26517131
inventory_2 Storage & Handling
Density 1.49 at 20℃
Storage 2-8°C

description Product Description

Used in research as a potent and selective inhibitor of anaplastic lymphoma kinase (ALK), particularly in the development of targeted cancer therapies. Shows promising activity against ALK-positive non-small cell lung cancer (NSCLC) by blocking abnormal signaling pathways that drive tumor growth. Also demonstrates effectiveness in overcoming resistance mutations in ALK, making it valuable in second-generation inhibitor design. Investigated for its blood-brain barrier penetration, supporting potential use in treating brain metastases associated with ALK-driven cancers. Currently utilized primarily in preclinical studies and drug development rather than clinical treatment.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,920.00
inventory 5g
10-20 days ฿22,150.00

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2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)pyrimidine-4,5,6-triamine
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Used in research as a potent and selective inhibitor of anaplastic lymphoma kinase (ALK), particularly in the development of targeted cancer therapies. Shows promising activity against ALK-positive non-small cell lung cancer (NSCLC) by blocking abnormal signaling pathways that drive tumor growth. Also demonstrates effectiveness in overcoming resistance mutations in ALK, making it valuable in second-generation inhibitor design. Investigated for its blood-brain barrier penetration, supporting potential use in treating brain metastases associated with ALK-driven cancers. Currently utilized primarily in preclinical studies and drug development rather than clinical treatment.
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