PDE11A4-IN-2
PDE11A4-IN-2 is a selective PDE11A4 inhibitor with an IC50 of 33 nM. PDE11A4-IN-2 functionally inhibits PDE11A4-mediated catalytic activities of cAMP and cGMP in cellular models. PDE11A4-IN-2 is applicable to the research of age-related cognitive decline.
For research use only. We do not sell to patients.
- Formula: C23H23FN8
- Molecular Weight:430.48
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
PDE11A4 33 nM (IC50) |
In Vitro
PDE11A4-IN-2 (compound 15c) exhibits moderate stability in mouse liver microsomes with a half-life of 25 min[1].
PDE11A4-IN-2 (0.1-100 μM) concentration-dependently inhibits cAMP- and cGMP-mediated catalytic activity of PDE11A4 in mouse HT22 hippocampal neuron cells overexpressing PDE11A4, with EC50 values of 10.2 μM and 10.4 μM, respectively, and does not alter the protein level of PDE11A4[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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Molecular Weight 430.48
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Formula C23H23FN8
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SMILES
CN(N=C1)C=C1C2=CN(C3CCN(CC#N)CC3)C4=NC=NC(NC5=CC(F)=CC=C5)=C42
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)