5-HT2AR ligand-2
5-HT2AR ligand-2 is a serotonin 2A receptor (5-HT2AR) ligand with a Ki value of 11.4 nM. 5-HT2AR ligand-2 stabilizes the inactive conformation of receptors by interacting with specific amino acid residues in the orthosteric binding pockets of D2R and 5-HT2AR, thereby blocking downstream signal transduction. 5-HT2AR ligand-2 can be used in studies related to schizophrenia.
For research use only. We do not sell to patients.
- Formula: C25H27F2N3O
- Molecular Weight:423.50
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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-HT2AR |
5-HT2AR ligand-2 (Compound 35) (0.1 nM-10 μM; 90 min) exhibits specific binding activity to 5-HT2AR in membrane fragments of cells stably expressing the specific receptor (including CHO, HEK T*, HET T, fibroblast), with a Ki value of 11.4 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
SYA16263 (5.91-17.73 mg/kg; i.p.; single administration; 60-66 min) does not induce extrapyramidal side effects in the rat catalepsy test model[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague-Dawley (male, ~ 6 weeks old, 133-153 g)[1]
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Dosage:5.91 mg/kg, 11.82 mg/kg, 17.73 mg/kg
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Administration:i.p.; single administration; 60, 63, 66 min
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Result:Showed no significant cataleptic response in either the bar test or CLP test across all doses compared with vehicle controls.
Enabled all animals to successfully right themselves during the righting reflex test, indicating no marked impairment.
Chemical Information
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Molecular Weight 423.50
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Formula C25H27F2N3O
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SMILES
OC(C1=CC=C(F)C=C1)(CCCN2CCN(C3=NC=CC=C3)CC2)C4=CC=C(F)C=C4
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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)