Nature 1987-01-01

Highly potent and selective ligands for histamine H3-receptors.

J M Arrang, M Garbarg, J C Lancelot, J M Lecomte, H Pollard, M Robba, W Schunack, J C Schwartz

文献索引:Nature 327 , 117, (1987)

全文:HTML全文

摘要

New drugs selective for histamine H3-receptors can be used to establish that these receptors are involved in the feedback control of histamine synthesis and release, and to demonstrate their distribution in the brain and peripheral tissues. These drugs provide new tools for affecting physiological and possibly pathological conditions in which histamine is involved.


相关化合物

  • R-(−)-α-Methylhis...
  • 硫丙咪胺马来酸

相关文献:

Effects of the histamine H3-agonist (R)-alpha-methylhistamine and the antagonist thioperamide on histamine metabolism in the mouse and rat brain.

1989-05-01

[J. Neurochem. 52 , 1388, (1989)]

Structure-activity relations of histamine analogs. XX. Absolute configuration and histamine-like activity of enantiomeric α-methyl histamines. Gerhard, et al.

[Arch. Pharm. Res. 313 , 709, (1980)]

更多文献...