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PKR1 antagonist 1
Catalog No. T201456 Copy Product Info
Purity: 99.47%
🥰Excellent
PKR1 antagonist 1 (PC1) is a potent PKR1 antagonist that effectively alleviates hyperalgesia and allodynia in SNI mice. PKR1 antagonist 1 can be used in research on pain, inflammation, and neurobiology.
PKR1 antagonist 1
Copy Product Info🥰Excellent
Catalog No. T201456
PKR1 antagonist 1 (PC1) is a potent PKR1 antagonist that effectively alleviates hyperalgesia and allodynia in SNI mice. PKR1 antagonist 1 can be used in research on pain, inflammation, and neurobiology.
Cas No. 910113-60-9
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $367 | - | In Stock | |
| 5 mg | $868 | - | In Stock | |
| 10 mg | $1,170 | - | In Stock | |
| 25 mg | $1,730 | - | In Stock | |
| 50 mg | $2,350 | - | In Stock |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.47%
Appearance:Solid
Color:White
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | PKR1 antagonist 1 (PC1) is a potent PKR1 antagonist that effectively alleviates hyperalgesia and allodynia in SNI mice. PKR1 antagonist 1 can be used in research on pain, inflammation, and neurobiology. |
| In vivo | Methods: To investigate the analgesic effects of PKR1 antagonist 1, a spared nerve injury (SNI) mouse model was used. From day 1 to day 8 post-surgery, mice were administered PKR1 antagonist 1 (150 μg/kg) subcutaneously twice daily for 8 consecutive days. Results: PKR1 antagonist 1 completely prevented thermal allodynia, mechanosensory-induced pain, and dynamic mechanosensory pain. Pain returned in the mice 2–3 days after discontinuation of the drug.[1] |
| Molecular Weight | 451.52 |
| Formula | C23H29N7O3 |
| Cas No. | 910113-60-9 |
| Smiles | O=C1N=C(NCCNC(=N)N)N(C(=O)N1CC2=CC=C(C=C2)CC)CC3=CC=C(OC)C=C3 |
| 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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
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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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