Name | 1-(2-naphthalen-2-ylethyl)-4-[3-(trifluoromethyl)phenyl]-3,6-dihydro-2H-pyridine,hydrochloride |
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Synonyms | Xaliproden hydrochloride |
Description | Xaliproden hydrochloride (SR57746A) is a potent, selective and orally active agonist of 5-HT1A receptor, shows a high affinity for 5-HT1A specific binding sites in the rat hippocampus (IC50=3 nM). Xaliproden hydrochloride is also a selective antagonist of dopamine D2 receptor, has moderate affinity (IC50=0.1-1 μM). Xaliproden hydrochloride exhibits anti-depression and anti-anxiety effects, and it may possess therapeutic potential for the research of neurodegenerative diseases[1][2][3]. |
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Related Catalog | |
Target |
5-HT1A Receptor:3 nM (IC50) D2 Receptor:0.1-1 μM (IC50) |
References |
Boiling Point | 487.8ºC at 760mmHg |
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Molecular Formula | C24H23ClF3N |
Molecular Weight | 417.89400 |
Flash Point | 248.8ºC |
Exact Mass | 417.14700 |
PSA | 3.24000 |
LogP | 6.93030 |