Description
A selective AT2 receptor antagonist (IC50s = 39.5 and 408,000 nM for rat recombinant AT2 and AT1, respectively); inhibits capsaicin-induced calcium influx in cultured hDRG neurons (IC50 = 10 nM); reduces neurite density and length in rat DRG neuronal cultures; has analgesic effects in a rat model of neuropathic pain induced by chronic constriction injury
Formal name: (3S)-2-(2,2-diphenylacetyl)-1,2,3,4-tetrahydro-6-methoxy-5-(phenylmethoxy)-3-isoquinolinecarboxylic acid
Synonyms:
Molecular weight: 507.6
CAS: 1316755-16-4
Purity: ≥95%
Formulation: A crystalline solid
Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Neuroscience|Pain Research