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Liarozole dihydrochloride

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Catalog No. T11847Cas No. 1883548-96-6
Alias R75251 dihydrochloride

Liarozole dihydrochloride is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.

Liarozole dihydrochloride

Liarozole dihydrochloride

😃Good
Catalog No. T11847Alias R75251 dihydrochlorideCas No. 1883548-96-6
Liarozole dihydrochloride is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.
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10 mg$63835 days
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Product Introduction

Bioactivity
Description
Liarozole dihydrochloride is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.
Targets&IC50
CYP26:7 μM (IC50)
In vitro
Liarozole inhibits 17a-hydroxylase activity in bovine adrenal microsomes (IC50=0.15 μM) [1]. Liarozole has modest inhibitory activity on cholesterol synthesis in human hepatoma cells(IC50=5 μM)[1].Liarozole inhibits the metabolism of retinoic acid to more polar metabolites in hamster liver microsomes (IC50=2.2 μM), rat liver homogenate (IC50=0.14 μM), dunning prostate cancer homogenate (IC50=0.26 μM) and MCF-7 human breast cancer cells (almost complete block at 10μM) [1].
AliasR75251 dihydrochloride
Chemical Properties
Molecular Weight381.69
FormulaC17H15Cl3N4
Cas No.1883548-96-6
Relative Density.no data available
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 (131.00 mM), Sonication is recommended.
H2O: 50 mg/mL (131.00 mM)
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.6199 mL13.0996 mL26.1993 mL130.9964 mL
5 mM0.5240 mL2.6199 mL5.2399 mL26.1993 mL
10 mM0.2620 mL1.3100 mL2.6199 mL13.0996 mL
20 mM0.1310 mL0.6550 mL1.3100 mL6.5498 mL
50 mM0.0524 mL0.2620 mL0.5240 mL2.6199 mL
100 mM0.0262 mL0.1310 mL0.2620 mL1.3100 mL

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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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