PSB-10211
PSB-10211 is a P2X2 receptor antagonist with an IC50 of 0.086 μM against rat P2X2 receptors. PSB-10211 inhibits ATP-mediated currents of rat P2X2 receptors expressed in Xenopus oocytes. PSB-10211 can be used in studies related to pain and urinary incontinence.
For research use only. We do not sell to patients.
- CAS No.: 66295-57-6
- Formula: C23H13Cl2N6NaO5S
- Molecular Weight:579.35
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All P2X Receptor Isoforms
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Biological Activity
Description
In Vitro
PSB-10211 inhibits human P2Y2 receptor-mediated calcium mobilization with an IC50 of 24.3 μM, shows inhibitory activity with an IC50 of ~10 μM at human P2Y4 receptors, and shows inhibitory activity at concentrations >10 μM at rat P2Y6 receptors[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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CAS No. 66295-57-6
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Molecular Weight 579.35
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Formula C23H13Cl2N6NaO5S
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SMILES
O=C1C2=C(C(C3=C(C(S(=O)(O[Na])=O)=CC(NC4=CC(NC5=NC(Cl)=NC(Cl)=N5)=CC=C4)=C13)N)=O)C=CC=C2
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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)