Description
A selective, orally bioavailable antagonist of the EP1 receptor (Ki = 1.9 nM); suppresses pain associated with cyclophosphamide-induced cystitis in mice
Formal name: 4-[[[2,3-dihydro-6-[(2-methylpropyl)[(4-methyl-2-thiazolyl)sulfonyl]amino]-1H-inden-5-yl]oxy]methyl]-benzoic acid
Synonyms:
Molecular weight: 500.6
CAS: 459841-96-4
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway||Research Area|Neuroscience|Pain Research