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Crizotinib hydrochloride

Catalog No. T8399   CAS 1415560-69-8
Synonyms: PF-02341066 hydrochloride

Crizotinib hydrochloride (PF-02341066 hydrochloride) is a novel inhibitor of anaplastic lymphoma kinase and c-Met(IC50s of 20 and 8 nM)

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Crizotinib hydrochloride Chemical Structure
Crizotinib hydrochloride, CAS 1415560-69-8
Pack Size Availability Price/USD Quantity
5 mg In stock $ 31.00
10 mg In stock $ 48.00
25 mg In stock $ 75.00
50 mg In stock $ 101.00
100 mg In stock $ 140.00
200 mg In stock $ 174.00
500 mg In stock $ 239.00
1 mL * 10 mM (in DMSO) In stock $ 54.00
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Purity: 99.67%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Crizotinib hydrochloride (PF-02341066 hydrochloride) is a novel inhibitor of anaplastic lymphoma kinase and c-Met(IC50s of 20 and 8 nM)
Targets&IC50 ALK:20 nM , c-Met:8 nM
In vitro Crizotinib hydrochloride(PF-2341066)potently inhibited NPM-ALK phosphorylation in Karpas299 or SU-DHL-1 ALCL cells (mean IC(50) value, 24 nmol/L).?In biochemical and cellular screens, PF-2341066 was shown to be selective for c-Met and ALK at pharmacologically relevant concentrations across a panel of >120 diverse kinases.?PF-2341066 potently inhibited cell proliferation, which was associated with G(1)-S-phase cell cycle arrest and induction of apoptosis in ALK-positive ALCL cells (IC(50) values, approximately 30 nmol/L) but not ALK-negative lymphoma cells[1].
Synonyms PF-02341066 hydrochloride
Molecular Weight 486.8
Formula C21H23Cl3FN5O
CAS No. 1415560-69-8

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 4.9 mg/mL (10.07 mM)

H2O: 50 mg/mL (102.71 mM), Sonification is recommended.

TargetMolReferences and Literature

1. Christensen JG, et al. Cytoreductive antitumor activity of PF-2341066, a novel inhibitor of anaplastic lymphoma kinase and c-Met, in experimental models of anaplastic large-cell lymphoma. Mol Cancer Ther. 2007, 6(12 Pt 1), 3314-3322. 2. Cui JJ, et al. Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK). J Med Chem. 2011 Sep 22;54(18):6342-63.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Approved Drug Library Inhibitor Library Anti-Cancer Drug Library Anti-Cancer Clinical Compound Library Anti-Cancer Active Compound Library EMA Approved Drug Library Tyrosine Kinase Inhibitor Library Drug Repurposing Compound Library FDA-Approved Kinase Inhibitor Library Kinase Inhibitor Library

Related Products

Related compounds with same targets
Crizotinib Lorlatinib Taletrectinib Salvigenin Taletrectinib free base ROS kinases-IN-2 Methyl 12-methyltridecanoate ROS-generating agent 1

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Keywords

Crizotinib hydrochloride 1415560-69-8 Angiogenesis Autophagy Immunology/Inflammation Tyrosine Kinase/Adaptors c-Met/HGFR ROS ALK ROS Kinase Crizotinib Hydrochloride PF02341066 Hydrochloride CD246 PF-02341066 PF 02341066 Hydrochloride ALK tyrosine kinase receptor Anaplastic lymphoma kinase (ALK) PF02341066 PF 02341066 Crizotinib Cluster of differentiation 246 Inhibitor PF-02341066 Hydrochloride inhibit Anaplastic lymphoma kinase PF-02341066 hydrochloride inhibitor

 

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