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(S)-crizotinib

(S)-crizotinib
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Purity:99.89%
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(S)-crizotinib

Catalog No. T6357Cas No. 1374356-45-2
(S)-crizotinib (ent-crizotinib) (IC50 of 72 nM), an effective MTH1 (NUDT1) inhibitor, is the (S)-enantiomer of crizotinib.
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Pack SizePriceAvailabilityQuantity
2 mg$39In Stock
5 mg$64In Stock
10 mg$97In Stock
25 mg$162In Stock
50 mg$239In Stock
100 mg$372In Stock
1 mL x 10 mM (in DMSO)$70In Stock
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Product Introduction

Bioactivity
Description
(S)-crizotinib (ent-crizotinib) (IC50 of 72 nM), an effective MTH1 (NUDT1) inhibitor, is the (S)-enantiomer of crizotinib.
In vitro
In the SW480 colorectal cancer model, daily oral administration of 50mg/kg (S)-Crizotinib effectively inhibits tumor growth.
In vivo
(S)-crizotinib activates DNA repair mechanisms in human colorectal cancer cells by inhibiting MTH1, thereby disrupting nucleotide pool homeostasis and further inducing an increase in DNA single-strand breaks.
Kinase Assay
MTH1 catalytic assay: Half-maximal inhibitory concentrations (IC50) are determined using a luminescence-based assay with some minor modifications. Briefly, serial dilutions of compounds are dissolved in assay buffer (100?mM Tris-acetate pH?7.5, 40?mM NaCl and 10?mM Mg(OAc)2 containing 0.005% Tween-20 and 2?mM dithiothreitol (DTT). Upon addition of MTH1 recombinant protein (final concentration 2?nM), plates are incubated on a plate shaker for 15?min at room temperature. After addition of the substrate dGTP (final concentration 100?μM), 8-oxo-dGTP (final concentration 13.2?μM), or 2-OH-dATP (final concentration 8.3?μM) the generation of pyrophosphate (PPi) as a result of nucleotide triphosphate hydrolysis by MTH1 is monitored over a time course of 15?min using the PPi Light Inorganic Pyrophosphate Assay kit. IC50 values are determined by fitting a dose-response curve to the data points using nonlinear regression analysis using the GraphPad Prism software.
Cell Research
One day before treatment, cells are seeded per well in six-well plates and incubated for 24 h. The next day DMSO (equal to highest amount of compound dilution, maximum 0.2%) or compounds in increasing concentrations were added and cells incubated at 37 °C, 5% CO2, for 7-10 days. After washing with PBS, cells are fixed with ice-cold methanol, stained with crystal violet solution (0.5% in 25% methanol) and left to dry overnight. For quantification of results, ultraviolet absorbance of crystal violet is determined at 595 nm following solubilisation by 70% ethanol. Data are analysed using nonlinear regression analysis using the GraphPad Prism software. (Only for Reference)
Aliasent-crizotinib
Chemical Properties
Molecular Weight450.34
FormulaC21H22Cl2FN5O
Cas No.1374356-45-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
1eq. HCl: 9 mg/mL (20 mM))
DMSO: 22.5 mg/mL (50 mM)
Solution Preparation Table
DMSO/1eq. HCl
1mg5mg10mg50mg
1 mM2.2205 mL11.1027 mL22.2054 mL111.0272 mL
5 mM0.4441 mL2.2205 mL4.4411 mL22.2054 mL
10 mM0.2221 mL1.1103 mL2.2205 mL11.1027 mL
DMSO
1mg5mg10mg50mg
20 mM0.1110 mL0.5551 mL1.1103 mL5.5514 mL
50 mM0.0444 mL0.2221 mL0.4441 mL2.2205 mL
100 mM0.0222 mL0.1110 mL0.2221 mL1.1103 mL

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