Description
A dibenzoxazepine which acts as a selective antagonist of PGE2 at the human EP1 receptor (IC50 = 6.7 µM); at doses between 0.3-300 µM, is a competitive antagonist of PGE2-induced smooth muscle contractions of guinea pig ileum and stomach and trachea
Formal name: 8-chloro-dibenz[b,f][1,4]oxazepine-10(11H)-carboxy-(2-acetyl)hydrazide
Synonyms:
Molecular weight: 331.8
CAS: 19395-87-0
Purity: ≥96%
Formulation: A crystalline solid
Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway||Research Area|Neuroscience|Neurodegenerative Disorders|Parkinson’s Disease