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AZM475271

Catalog No. T14487Cas No. 476159-98-5
Alias M475271

AZM475271 is a potent and selective inhibitor of Src kinase (IC50: 5 nM).

AZM475271

AZM475271

Purity: 99.78%
Catalog No. T14487Alias M475271Cas No. 476159-98-5
AZM475271 is a potent and selective inhibitor of Src kinase (IC50: 5 nM).
Pack SizePriceAvailabilityQuantity
2 mg$29In Stock
1 mL x 10 mM (in DMSO)$80In Stock
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Purity:99.78%
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Product Introduction

Bioactivity
Description
AZM475271 is a potent and selective inhibitor of Src kinase (IC50: 5 nM).
In vitro
AZM475271 demonstrated strong dose-dependent inhibition of Src tyrosine kinase activity in the L3.6pl human pancreatic carcinoma cell line. The IC50 concentration of AZM475271 to inhibit the phosphorylation of c-src, lck, and c-yes was 0.01, 0.03, and 0.08 μmol/L, respectively, in comparison with an IC50 of 0.7 μmol/L AZM475271 to inhibit KDR [2]. Maximum reduction of Src kinase activity was observed after incubation for 4 hours with ≥5 μmol/L.
In vivo
Treatment with gemcitabine or AZM475271 alone did not significantly change animal weight [2]. In vivo: Tumors appeared to be palpable at day 14 after tumor cell injection in all animals except mice treated with both AZM475271 and gemcitabine, in which the earliest possible palpation of the tumors was at day 17 after tumor cell injection.
AliasM475271
Chemical Properties
Molecular Weight442.94
FormulaC23H27ClN4O3
Cas No.476159-98-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 42 mg/mL (94.82 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2576 mL11.2882 mL22.5764 mL112.8821 mL
5 mM0.4515 mL2.2576 mL4.5153 mL22.5764 mL
10 mM0.2258 mL1.1288 mL2.2576 mL11.2882 mL
20 mM0.1129 mL0.5644 mL1.1288 mL5.6441 mL
50 mM0.0452 mL0.2258 mL0.4515 mL2.2576 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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