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Canertinib dihydrochloride

🥰Excellent
Catalog No. T2501Cas No. 289499-45-2
Alias PD-183805 dihydrochloride, CI-1033 dihydrochloride

Canertinib dihydrochloride (PD-183805 dihydrochloride) is the hydrochloride salt of an orally bio-available quinazoline with potential antineoplastic and radiosensitizing activities.

Canertinib dihydrochloride

Canertinib dihydrochloride

🥰Excellent
Purity: 99.23%
Catalog No. T2501Alias PD-183805 dihydrochloride, CI-1033 dihydrochlorideCas No. 289499-45-2
Canertinib dihydrochloride (PD-183805 dihydrochloride) is the hydrochloride salt of an orally bio-available quinazoline with potential antineoplastic and radiosensitizing activities.
Pack SizePriceAvailabilityQuantity
10 mg$30In Stock
25 mg$35In Stock
50 mg$45In Stock
1 mL x 10 mM (in DMSO)$30In Stock
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Purity:99.23%
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Product Introduction

Bioactivity
Description
Canertinib dihydrochloride (PD-183805 dihydrochloride) is the hydrochloride salt of an orally bio-available quinazoline with potential antineoplastic and radiosensitizing activities.
Targets&IC50
EGFR:7.4nM, ErbB2:9 nM
Kinase Assay
Kinase inhibition: Cediranib is dissolved in DMSO at a concentration of 10 mM. All enzyme assays are run at, or just below, the respective Km for ATP (0.2 - 30 μM). The inhibitory activity of Cediranib is determined against a range of recombinant tyrosine kinases [KDR, Flt-1, Flt-4, c-Kit, PDGFRα, PDGFRβ, CSF-1R, Flt-3, FGFR1, Src, Abl, epidermal growth factor receptor (EGFR), ErbB2, Aurora A, and Aurora B] using ELISA. Selectivity versus CDK2 and CDK4 serine/threonine kinases is examined using scintillation proximity assays with a retinoblastoma substrate and [γ-sup>33P]ATP. Activity of Cediranib is compared to MAPK kinase (MEK), which shows dual specificity. It is determined using a MAPK substrate, [γ-33P]ATP, and paper capture/scintillation counting.
AliasPD-183805 dihydrochloride, CI-1033 dihydrochloride
Chemical Properties
Molecular Weight558.86
FormulaC24H27Cl3FN5O3
Cas No.289499-45-2
SmilesCl.Cl.Fc1ccc(Nc2ncnc3cc(OCCCN4CCOCC4)c(NC(=O)C=C)cc23)cc1Cl
Relative Density.1.355g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 55.9 mg/mL (100 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.7894 mL8.9468 mL17.8936 mL89.4678 mL
5 mM0.3579 mL1.7894 mL3.5787 mL17.8936 mL
10 mM0.1789 mL0.8947 mL1.7894 mL8.9468 mL
20 mM0.0895 mL0.4473 mL0.8947 mL4.4734 mL
50 mM0.0358 mL0.1789 mL0.3579 mL1.7894 mL
100 mM0.0179 mL0.0895 mL0.1789 mL0.8947 mL

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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:
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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
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