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WR99210
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Catalog No. T17257Cas No. 47326-86-3
Alias WR-99210, WR 99210, BRL 6231 free base
WR99210 (BRL 6231 free base) is an orally available dihydrofolate reductase (DHFR) inhibitor with antiparasitic activity, often used in combination with dapsone to study Mycobacterium avium complex (MAC).
WR99210
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Purity: 98.8%
Catalog No. T17257Alias WR-99210, WR 99210, BRL 6231 free baseCas No. 47326-86-3
WR99210 (BRL 6231 free base) is an orally available dihydrofolate reductase (DHFR) inhibitor with antiparasitic activity, often used in combination with dapsone to study Mycobacterium avium complex (MAC).
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $59 | - | In Stock | |
| 5 mg | $142 | - | In Stock | |
| 10 mg | $222 | - | In Stock | |
| 25 mg | $453 | - | In Stock | |
| 50 mg | $739 | - | In Stock | |
| 100 mg | $987 | - | In Stock | |
| 500 mg | $1,980 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.8%
Appearance:Solid
Color:White
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | WR99210 (BRL 6231 free base) is an orally available dihydrofolate reductase (DHFR) inhibitor with antiparasitic activity, often used in combination with dapsone to study Mycobacterium avium complex (MAC). |
| Targets&IC50 | DHFR:<0.075 nM |
| In vitro | WR99210 (0-100 nM; 92 h) showed significant inhibition of tachyzoites of T. gondii in tissue culture. [1] WR99210 (0-100 nM; 92 h) shows low cytotoxicity to human foreskin fibroblasts. [1] |
| In vivo | In a mouse model, WR99210 (1.25 mg/kg; intraperitoneal injection; once daily for 5 consecutive days) exhibited a significant inhibitory effect on T. gondii tachyzoites. [1] |
| Synonyms | WR-99210, WR 99210, BRL 6231 free base |
| Molecular Weight | 394.68 |
| Formula | C14H18Cl3N5O2 |
| Cas No. | 47326-86-3 |
| Smiles | ClC=1C=C(Cl)C(OCCCON2C(=NC(=NC2(C)C)N)N)=CC1Cl |
| Relative Density. | 1.52 g/cm3 (Predicted) |
| Storage | keep away from moisture | Powder: -20°C for 3 years | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||
| Solubility Information | DMSO: 2 mg/mL (5.07 mM), Sonication is recommended. | |||||||||||||||
Solution Preparation Table | ||||||||||||||||
DMSO
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Calculator
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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
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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