Description
A 5-HT1A receptor agonist (Ki = 0.4 nM); selective for 5-HT1A over 5-HT1D, 5-HT2, dopamine D1 and D2, and α1- and α2-adrenergic receptors (Kis = 7.7, >1,000, >1,000, 36, >1,000, and >1,000 nM, respectively); inhibits forskolin-stimulated cAMP synthesis in CHO cells transfected with human 5-HT1A; induces hypothermia in mice (ED50 = 0.041 mg/kg); induces 5-HT syndrome as well as decreases accumulation of 5-HT and dopamine in rats (5 mg/kg); decreases arterial blood pressure and heart rate in a dose-dependent manner in spontaneously hypertensive rats; reverses isolation-induced aggression in mice,
Formal name: (8R)-8-(dipropylamino)-6,7,8,9-tetrahydro-3H-benz[e]indole-2-carbonitrile, monohydrochloride
Synonyms:
Molecular weight: 331.9
CAS: 149654-41-1
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Cardiovascular System|Cardiovascular Diseases|Hypertension||Research Area|Neuroscience