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AGN 194310

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Catalog No. T14143Cas No. 229961-45-9
Alias VTP-194310

AGN 194310 (VTP-194310) is a pan-antagonist for retinoic acid receptors (RARs), with Kd values of 3 nM, 2 nM, and 5 nM for RARα, RARβ, and RARγ, respectively[1][2].

AGN 194310

AGN 194310

😃Good
Catalog No. T14143Alias VTP-194310Cas No. 229961-45-9
AGN 194310 (VTP-194310) is a pan-antagonist for retinoic acid receptors (RARs), with Kd values of 3 nM, 2 nM, and 5 nM for RARα, RARβ, and RARγ, respectively[1][2].
Pack SizePriceAvailabilityQuantity
5 mg$5968-10 weeks
25 mg$1,7108-10 weeks
50 mg$2,2308-10 weeks
100 mg$3,3908-10 weeks
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Product Introduction

Bioactivity
Description
AGN 194310 (VTP-194310) is a pan-antagonist for retinoic acid receptors (RARs), with Kd values of 3 nM, 2 nM, and 5 nM for RARα, RARβ, and RARγ, respectively[1][2].
Targets&IC50
RARα:3 nM (kd), RARβ:2 nM (kd), RARγ:5 nM (kd)
In vitro
AGN194310 effectively inhibits colony formation in LNCaP, PC3, and DU-145 cells with IC50 values of 16 nM, 18 nM, and 34 nM, respectively[2]. At concentrations of 50 nM and 100 nM, both alone and combined with TTNPB, AGN194310 inhibits colony formation in these cell lines[2]. Additionally, treatment with AGN194310 (1 μM for 72 hours) results in 80% apoptosis in LNCaP cells[2].
In vivo
AGN 194310 (0.5 mg/kg/day; oral gavage; every day; for 10 days; female C57Bl/6J mice) treatment significantly increases granulocyte numbers across hematopoietic compartments and the frequency of granulocyte-progenitor cells in bone marrow[3].
AliasVTP-194310
Chemical Properties
Molecular Weight424.55
FormulaC28H24O2S
Cas No.229961-45-9
Relative Density.1.26 g/cm3 (Predicted)
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 (117.77 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3554 mL11.7772 mL23.5544 mL117.7718 mL
5 mM0.4711 mL2.3554 mL4.7109 mL23.5544 mL
10 mM0.2355 mL1.1777 mL2.3554 mL11.7772 mL
20 mM0.1178 mL0.5889 mL1.1777 mL5.8886 mL
50 mM0.0471 mL0.2355 mL0.4711 mL2.3554 mL
100 mM0.0236 mL0.1178 mL0.2355 mL1.1777 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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