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(R)-VX-11e

🥰Excellent
Catalog No. T78143Cas No. 1680187-43-2
Alias (R)-VX11e

(R)-VX-11e is an isomer of VX-11e, a potent and selective ERK2 inhibitor with potential to inhibit tumor growth.

(R)-VX-11e

(R)-VX-11e

🥰Excellent
Purity: 98.73%
Catalog No. T78143Alias (R)-VX11eCas No. 1680187-43-2
(R)-VX-11e is an isomer of VX-11e, a potent and selective ERK2 inhibitor with potential to inhibit tumor growth.
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2 mg$68 In Stock
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Purity:98.73%
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Product Introduction

Bioactivity
Description
(R)-VX-11e is an isomer of VX-11e, a potent and selective ERK2 inhibitor with potential to inhibit tumor growth.
Alias(R)-VX11e
Chemical Properties
Molecular Weight500.35
FormulaC24H20Cl2FN5O2
Cas No.1680187-43-2
SmilesCC=1C(C=2C=C(C(N[C@@H](CO)C3=CC(Cl)=CC=C3)=O)NC2)=NC(NC4=C(Cl)C=C(F)C=C4)=NC1
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: , < 1 mg/mL (insoluble or slightly soluble)

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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:
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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