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LY 43578

🥰Excellent
Catalog No. T27918Cas No. 26766-35-8
Alias LY-43578, LY43578

LY 43578 is an orally active aromatase inhibitor. LY43578 could inhibit O-demethylation of P-450-dependent p-nitroanisole and N-demethylation of ethylmorphine (IC50 of 0.3 and 5 μm, respectively) in rat liver microsomes. LY 43578 can be used to study neurological and cardiovascular diseases.

LY 43578

LY 43578

🥰Excellent
Purity: 99.62%
Catalog No. T27918Alias LY-43578, LY43578Cas No. 26766-35-8
LY 43578 is an orally active aromatase inhibitor. LY43578 could inhibit O-demethylation of P-450-dependent p-nitroanisole and N-demethylation of ethylmorphine (IC50 of 0.3 and 5 μm, respectively) in rat liver microsomes. LY 43578 can be used to study neurological and cardiovascular diseases.
Pack SizePriceAvailabilityQuantity
2 mg$30In Stock
5 mg$48In Stock
10 mg$77In Stock
25 mg$127In Stock
50 mg$187In Stock
100 mg$278In Stock
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Purity:99.62%
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Product Introduction

Bioactivity
Description
LY 43578 is an orally active aromatase inhibitor. LY43578 could inhibit O-demethylation of P-450-dependent p-nitroanisole and N-demethylation of ethylmorphine (IC50 of 0.3 and 5 μm, respectively) in rat liver microsomes. LY 43578 can be used to study neurological and cardiovascular diseases.
AliasLY-43578, LY43578
Chemical Properties
Molecular Weight331.2
FormulaC17H12Cl2N2O
Cas No.26766-35-8
SmilesC(O)(C1=CC=C(Cl)C=C1)(C2=CC=C(Cl)C=C2)C=3C=NC=NC3
Relative Density.1.376g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 45 mg/mL (135.87 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0193 mL15.0966 mL30.1932 mL150.9662 mL
5 mM0.6039 mL3.0193 mL6.0386 mL30.1932 mL
10 mM0.3019 mL1.5097 mL3.0193 mL15.0966 mL
20 mM0.1510 mL0.7548 mL1.5097 mL7.5483 mL
50 mM0.0604 mL0.3019 mL0.6039 mL3.0193 mL
100 mM0.0302 mL0.1510 mL0.3019 mL1.5097 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
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