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].
Molekulargewicht:
417.89
Reinheit:
98.57
CAS Nummer:
[90494-79-4]
Formel:
C24H23ClF3N
Target-Kategorie:
5-HT Receptor,Dopamine Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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