Description
A potent and selective non-peptide OX1R antagonist (Kd = 5.03 and 3.76 nM in whole cell binding and membrane-based assays, respectively); >100-fold selective for OX1 over OX2 in calcium mobilization; no significant affinity for serotonergic, dopaminergic, adrenergic, or purinergic receptors
Formal name: [5-(2-fluorophenyl)-2-methyl-4-thiazolyl][(2S)-2-[(5-phenyl-1,3,4-oxadiazol-2-yl)methyl]-1-pyrrolidinyl]-methanone
Synonyms:
Molecular weight: 448.5
CAS: 483313-22-0
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Neuroscience