STEREOSELECTIVITY OF THE HISTAMINE H3-PRESYNAPTIC AUTORECEPTOR

被引:57
作者
ARRANG, JM [1 ]
SCHWARTZ, JC [1 ]
SCHUNACK, W [1 ]
机构
[1] FREE UNIV BERLIN,INST PHARM,D-1000 BERLIN 33,FED REP GER
关键词
D O I
10.1016/0014-2999(85)90478-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
引用
收藏
页码:109 / 114
页数:6
相关论文
共 17 条
[1]   ACTIONS OF BETAHISTINE AT HISTAMINE-RECEPTORS IN THE BRAIN [J].
ARRANG, JM ;
GARBARG, M ;
QUACH, TT ;
TUONG, MDT ;
YERAMIAN, E ;
SCHWARTZ, JC .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 111 (01) :73-84
[2]   AUTO-INHIBITION OF BRAIN HISTAMINE-RELEASE MEDIATED BY A NOVEL CLASS (H-3) OF HISTAMINE-RECEPTOR [J].
ARRANG, JM ;
GARBARG, M ;
SCHWARTZ, JC .
NATURE, 1983, 302 (5911) :832-837
[3]   AUTO-REGULATION OF HISTAMINE-RELEASE IN BRAIN BY PRESYNAPTIC H-3-RECEPTORS [J].
ARRANG, JM ;
GARBARG, M ;
SCHWARTZ, JC .
NEUROSCIENCE, 1985, 15 (02) :553-562
[4]  
ARRANG JM, 1985, FRONTIERS HISTAMINE, P143
[5]  
CHENG Y, 1973, BIOCHEM PHARMACOL, V22, P3099
[6]   IMPROMIDINE (SK AND F 92676) IS A VERY POTENT AND SPECIFIC AGONIST FOR HISTAMINE H-2 RECEPTORS [J].
DURANT, GJ ;
DUNCAN, WAM ;
GANELLIN, CR ;
PARSONS, ME ;
BLAKEMORE, RC ;
RASMUSSEN, AC .
NATURE, 1978, 276 (5686) :403-405
[7]  
Ganellin C. R., 1982, CHEM STRUCTURE ACTIV, P10
[8]  
GARBARG M, 1983, METHODS BIOGENIC AMI, P623
[10]   STRUCTURE-ACTIVITY RELATIONSHIP OF HISTAMINE ANALOGS .22. ABSOLUTE-CONFIGURATION AND HISTAMINE-LIKE ACTIVITY OF THE ENANTIOMERIC-ALPHA,NALPHA-DIMETHYLHISTAMINES [J].
GERHARD, G ;
SCHUNACK, W .
ARCHIV DER PHARMAZIE, 1980, 313 (09) :780-784