CP 132484
CP 132484 is a rat 5-HT2A receptor agonist with a Ki of 1.1 nM and an IC50 of 2.8 nM, and it exhibits over 40-fold selectivity over rat 5-HT1A receptors and bovine 5-HT1D receptors. CP 132484 stimulates phosphoinositide hydrolysis and intracellular calcium mobilization. CP 132484 can be used for research into diseases such as glaucoma.
For research use only. We do not sell to patients.
- CAS No.: 143508-76-3
- Formula: C14H18N2O
- Molecular Weight:230.31
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All 5-HT Receptor Isoforms
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Biological Activity
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5-HT2A Receptor 1.1 nM (Ki) |
5-HT2A Receptor 2.8 nM (IC50) |
CP 132484 (Compound 4a) (1 h) binds with high affinity to rat cortical 5-HT2A receptors, with a Ki of 1.1 nM and an IC50 of 2.8 nM[1].
CP 132484 (1 h) potently stimulates phosphoinositide hydrolysis in A7r5 rat vascular smooth muscle cells via activation of the 5-HT2A receptor, with an EC50 of 213 nM and a potency reaching 96% relative to serotonin[1].
CP 132484 stimulates calcium mobilization in A7r5 rat vascular smooth muscle cells by activating the 5-HT2a receptor, with an EC50 of 95.5 nM and a potency equivalent to 70% of that of serotonin[1].
CP 132484 (1 h) exhibits low affinity (IC50 = 8410 nM) and no agonist activity at cloned human 5-HT1A receptors expressed on CHO cell membranes[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 143508-76-3
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Molecular Weight 230.31
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Formula C14H18N2O
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SMILES
O1C2=CC=C3C(C(=CN3C)CCN)=C2CCC1
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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.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)