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
相关文献:
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)]