Description
A G protein-biased agonist of dopamine D2 receptors (EC50 = 0.37 μM in a calcium mobilization assay); inhibits forskolin-induced cAMP accumulation in CHO cells expressing human D2 receptors (EC50 = 0.26 μM) but is inactive in β-arrestin recruitment assays; antagonizes dopamine-induced β-arrestin recruitment in cell-based assays (IC50s = 3.8-9.9 μM); inhibitor of type II secretion in Gram-negative bacteria; inhibits secretion of phospholipase C (PlcH/N) and the virulence factor elastase (LasB) from P. aeruginosa (IC50s = 15 and 13 μM, respectively) and inhibits B. pseudomallei protease secretion by 90.8% at 25 μM
Formal name: 5-chloro-7-[[4-(2-pyridinyl)-1-piperazinyl]methyl]-8-quinolinol
Synonyms:
Molecular weight: 354.8
CAS: 315698-36-3
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Bacterial Diseases||Research Area|Neuroscience