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trifarotene

trifarotene
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Purity:99.78%
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trifarotene

Catalog No. T7586Cas No. 895542-09-3
Trifarotene (CD5789) is a potent and selective RARγ agonist, exhibiting 65-fold and 16-fold selectivity for RARγ (EC50=7.7 nM) over RARα (EC50=500 nM) and RARβ (EC50=125 nM).
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Pack SizePriceAvailabilityQuantity
2 mg$36In Stock
5 mg$58In Stock
10 mg$98In Stock
25 mg$163In Stock
50 mg$297In Stock
100 mg$496In Stock
1 mL x 10 mM (in DMSO)$59In Stock
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Product Introduction

Bioactivity
Description
Trifarotene (CD5789) is a potent and selective RARγ agonist, exhibiting 65-fold and 16-fold selectivity for RARγ (EC50=7.7 nM) over RARα (EC50=500 nM) and RARβ (EC50=125 nM).
Targets&IC50
RARγ:7.7 nM (EC50), RARβ:125 nM (EC50), RARα:500 nM (EC50)
In vitro
Administration of trifarotene involves in keratinization, desquamation, cornification and cell adhesion in reconstructed human epidermis (RHE) with the mean EC50 on the combined target genes of 0.0048%[2].
In vivo
In rhino mice, administration of 0.001%-0.01% Trifarotene shows dose-dependent comedolytic activity. Being fully efficacious at 0.01% with reduction of 98%[2].
AliasCD5789
Chemical Properties
Molecular Weight459.58
FormulaC29H33NO4
Cas No.895542-09-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 200 mg/mL (435.18 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1759 mL10.8795 mL21.7590 mL108.7950 mL
5 mM0.4352 mL2.1759 mL4.3518 mL21.7590 mL
10 mM0.2176 mL1.0879 mL2.1759 mL10.8795 mL
20 mM0.1088 mL0.5440 mL1.0879 mL5.4397 mL
50 mM0.0435 mL0.2176 mL0.4352 mL2.1759 mL
100 mM0.0218 mL0.1088 mL0.2176 mL1.0879 mL

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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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