(Partial) agonist/antagonist properties of novel diarylalkyl carbamates on histamine H 3 receptors

This publication has 29 references indexed in Scilit:

• Novel Partial Agonists for the Histamine H₃ Receptor with High in Vitro and in Vivo Activity
  Journal of Medicinal Chemistry, 1999
• Cloning and Functional Expression of the Human Histamine H₃Receptor
  Molecular Pharmacology, 1999
• Therapeutic potential of histamine H3 receptor agonists and antagonists
  Trends in Pharmacological Sciences, 1998
• Imetit and N-methyl derivatives. The transition from potent agonist to antagonist at histamine H3 receptors.1
  Bioorganic & Medicinal Chemistry Letters, 1992
• Isothiourea analogues of histamine as potent agonists or antagonists of the histamine H3-receptor
  European Journal of Medicinal Chemistry, 1992
• Two novel, potent and selective histamine H3 receptor agonists
  Bioorganic & Medicinal Chemistry Letters, 1992
• Autoinhibition of histamine synthesis mediated by presynaptic H3-receptors
  Neuroscience, 1987
• Highly potent and selective ligands for histamine H3-receptors
  Nature, 1987
• Autoregulation of histamine release in brain by presynaptic H3-receptors
  Neuroscience, 1985
• Auto-inhibition of brain histamine release mediated by a novel class (H3) of histamine receptor
  Nature, 1983