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EMI56

Catalog No. T35913Cas No. 2414374-41-5

EMI56, a derivative of EMI1, exhibits enhanced potency against mutant EGFR compared to EMI1. Additionally, EMI56 effectively inhibits EGFR triple mutants[1].

EMI56

EMI56

Catalog No. T35913Cas No. 2414374-41-5
EMI56, a derivative of EMI1, exhibits enhanced potency against mutant EGFR compared to EMI1. Additionally, EMI56 effectively inhibits EGFR triple mutants[1].
Pack SizePriceAvailabilityQuantity
2 mg$2335 days
5 mg$2975 days
25 mg$9166-8 weeks
50 mg$1,1906-8 weeks
100 mg$1,8606-8 weeks
1 mL x 10 mM (in DMSO)$3185 days
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Product Introduction

Bioactivity
Description
EMI56, a derivative of EMI1, exhibits enhanced potency against mutant EGFR compared to EMI1. Additionally, EMI56 effectively inhibits EGFR triple mutants[1].
In vitro
EMI56 inhibits EGFR ex19del/T790M/C797S and EGFR L858R/T790M/C797S and can be used in research of mutant EGFR-associated, drug-resistant non-small-cell lung cancer (NSCLC)[1]. EMI56 (10, 15, 20 μM; 2 h of treatment) strongly inhibits total EGFR levels, activation, and downstream signaling in PC9 EGFR ex19del/T790M/C797S cells[1].
Chemical Properties
Molecular Weight348.4
FormulaC21H20N2O3
Cas No.2414374-41-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (143.51 mM), Sonication and heating to 60℃ are recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8703 mL14.3513 mL28.7026 mL143.5132 mL
5 mM0.5741 mL2.8703 mL5.7405 mL28.7026 mL
10 mM0.2870 mL1.4351 mL2.8703 mL14.3513 mL
20 mM0.1435 mL0.7176 mL1.4351 mL7.1757 mL
50 mM0.0574 mL0.2870 mL0.5741 mL2.8703 mL
100 mM0.0287 mL0.1435 mL0.2870 mL1.4351 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:
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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