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FXR agonist 16
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Catalog No. T218430 Copy Product Info
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FXR agonist16 is an FXR agonist with an EC50 of 2.2 μM. It activates the transcriptional activity of FXR, leading to increased expression of SHP and BSEP, while reducing the expression of Cyp7a1. FXR agonist16 demonstrates hepatoprotective activity by decreasing AST and ALT levels in hepatocyte injury models induced by free fatty acids. This compound is useful in liver injury research.
FXR agonist 16
Cas No. 3099198-78-1
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | FXR agonist16 is an FXR agonist with an EC50 of 2.2 μM. It activates the transcriptional activity of FXR, leading to increased expression of SHP and BSEP, while reducing the expression of Cyp7a1. FXR agonist16 demonstrates hepatoprotective activity by decreasing AST and ALT levels in hepatocyte injury models induced by free fatty acids. This compound is useful in liver injury research. |
| In vitro | FXR agonist 16 (Compound 3q) acts as an FXR agonist in stably transfected HEK293 cells, with an EC50 of 2.2 μM when used at concentrations of 10-100 μM for 24 hours. Additionally, FXR agonist 16 demonstrates hepatoprotective activity in FFA-damaged AML12 cells at concentrations of 1-20 μM for 24 hours, reducing liver injury markers without significant cytotoxicity up to 25 μM. Furthermore, it modulates the expression of FXR downstream target genes in AML12 cells by upregulating SHP and BSEP while downregulating Cyp7a1 at concentrations of 1-10 μM. |
| Molecular Weight | 372.56 |
| Formula | C23H32O2S |
| Cas No. | 3099198-78-1 |
| Smiles | S([C@@]12[C@@]3([C@](C(C)(C)C3)(CC[C@@](C)(C1)CCC2)[H])[H])C4=C(C(OC)=O)C=CC=C4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
Dissolve 2 mg of the compound in 100 μL DMSO to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
Preparation of the In Vivo Formulation:
1) Add 100 μL of the DMSO stock solution to 400 µL PEG300 and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O and mix thoroughly until a homogeneous solution is obtained.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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Related Tags: FXR agonist 16 in vitro | FXR agonist 16 formula | FXR agonist 16 molecular weight
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