Description
A 5-HT1F receptor agonist (Kd =0.446 nM); selective for 5-HT1F over other G protein-coupled 5-HT receptor subtypes (Kis = 16.4->3,000 nM); inhibits forskolin-induced cAMP accumulation in mouse L-M(TK-) cell membranes expressing the recombinant human 5-HT1F receptor (EC50 = 1.51 nM); decreases electrically stimulated extravasation of plasma proteins in the dura mater in a guinea pig trigeminal nerve model of migraine headache.
Formal name: 4-fluoro-N-[3-(1-methyl-4-piperidinyl)-1H-indol-5-yl]-benzamide, monohydrochloride
Synonyms:
Molecular weight: 387.9
CAS: 199673-74-0
Purity: ≥98%
Formulation: A crystalline solid