Quaternised renzapride as a potent and selective 5-HT4 receptor agonist

This publication has 11 references indexed in Scilit:

• SC-53116: the first selective agonist at the newly identified serotonin 5-HT4 receptor subtype
  Journal of Medicinal Chemistry, 1992
• Benzimidazolone derivatives act as 5-HT4 receptor ligands in rat oesophagus
  European Journal of Pharmacology, 1992
• Peristalsis evoked by 5‐HT and renzapride: evidence for putative 5‐HT₄ receptor activation
  British Journal of Pharmacology, 1991
• Azabicycloalkyl benzimidazolones: Interaction with serotonergic 5-HT3 and 5-HT4 receptors and potential therapeutic implications
  Drugs of the Future, 1991
• Piglet sinoatrial 5-HT receptors resemble human atrial 5-HT4-like receptors
  Naunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1990
• Synthesis of a new class of 2,3-dihydro-2-oxo-1H-benzimidazole-1-carboxylic acid derivatives as highly potent 5-HT3 receptor antagonists
  Journal of Medicinal Chemistry, 1990
• The gastrointestinal prokinetic benzamide derivatives are agonists at the non-classical 5-HT receptor (5-HT4) positively coupled to adenylate cyclase in neurons
  Naunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1989
• [3H]-BRL 43694 (granisetron), a specific ligand for 5-HT3 binding sites in rat brain cortical membranes
  Biochemical Pharmacology, 1989
• Increased gut cholinergic activity and antagonism of 5‐hydroxytryptamine M‐receptors by BRL 24924: potential clinical importance of BRL 24924
  British Journal of Pharmacology, 1987
• Identification of serotonin M-receptor subtypes and their specific blockade by a new class of drugs
  Nature, 1985