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PDE4-IN-32
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Catalog No. T218188 Copy Product Info
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PDE4-IN-32 (Compound B05) is a selective inhibitor of PDE4B and PDE4D with the capacity to penetrate the blood-brain barrier, exhibiting IC50 values of 13.7 nM and 23.8 nM, respectively. It aids in motor and cognitive recovery in MCAO/R mouse models, reduces cerebral edema, and is applicable in ischemic stroke research.
PDE4-IN-32
Cas No. 3080627-61-5
| 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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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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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | PDE4-IN-32 (Compound B05) is a selective inhibitor of PDE4B and PDE4D with the capacity to penetrate the blood-brain barrier, exhibiting IC50 values of 13.7 nM and 23.8 nM, respectively. It aids in motor and cognitive recovery in MCAO/R mouse models, reduces cerebral edema, and is applicable in ischemic stroke research. |
| Targets & IC50 | PDE4B:13.7 nM |
| In vitro | PDE4-IN-32 is a potent and selective inhibitor of PDE4 subtypes, exhibiting an IC50 of 23.8 nM for PDE4D and 13.7 nM for PDE4B, with over 420-fold selectivity for other PDE subtypes. PDE4-IN-32 (0.156-1.25 μM; 1 h) dose-dependently protects HT-22 mouse hippocampal neuronal cells from OGD/R-induced damage. |
| In vivo | PDE4-IN-32 (60 mg/kg; oral; single dose) does not induce vomiting in adult male Beagle dogs. PDE4-IN-32 (2-30 mg/kg; intraperitoneal injection) reduces the infarct volume in male C57BL/6 mice within the MCAO/R model, and this reduction in infarct size is dose-dependent. |
| Molecular Weight | 320.34 |
| Formula | C20H16O4 |
| Cas No. | 3080627-61-5 |
| Smiles | O=C1OCC=2C=C(C=CC12)C=3C=CC(OC)=C4OC(=CC43)C5CC5 |
| 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
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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Related Tags: PDE4-IN-32 in vivo | PDE4-IN-32 in vitro | PDE4-IN-32 formula | PDE4-IN-32 molecular weight
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