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WDR5-47

Catalog No. T67697Cas No. 1422389-91-0

WDR5-47 is a potent small molecule to disturb the interaction of MLL1-WDR5 with IC50 value of 0.3μM.

WDR5-47

WDR5-47

Purity: 98.08%
Catalog No. T67697Cas No. 1422389-91-0
WDR5-47 is a potent small molecule to disturb the interaction of MLL1-WDR5 with IC50 value of 0.3μM.
Pack SizePriceAvailabilityQuantity
1 mg$117In Stock
5 mg$269In Stock
10 mg$395In Stock
25 mg$592In Stock
50 mg$828In Stock
100 mg$1,130In Stock
200 mg$1,520In Stock
1 mL x 10 mM (in DMSO)$293In Stock
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Purity:98.08%
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Product Introduction

Bioactivity
Description
WDR5-47 is a potent small molecule to disturb the interaction of MLL1-WDR5 with IC50 value of 0.3μM.
Targets&IC50
MLL1-WDR5:0.3 μM
Chemical Properties
Molecular Weight406.84
FormulaC19H20ClFN4O3
Cas No.1422389-91-0
Storage & Solubility Information
StorageShipping with blue ice.
Solubility Information
DMSO: 25 mg/mL (61.45 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4580 mL12.2898 mL24.5797 mL122.8984 mL
5 mM0.4916 mL2.4580 mL4.9159 mL24.5797 mL
10 mM0.2458 mL1.2290 mL2.4580 mL12.2898 mL
20 mM0.1229 mL0.6145 mL1.2290 mL6.1449 mL
50 mM0.0492 mL0.2458 mL0.4916 mL2.4580 mL

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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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