STUDIES ON ANNELATED 1,4-BENZOTHIAZINES AND 1,5-BENZOTHIAZEPINES .7. SYNTHESIS AND INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING OF SOME 4,5-DIHYDRO-TETRAZOLO[5,1-D]-1,5-BENZOTHIAZEPINES AND 5-PHENYL-S-TRIAZOLO[3,4-D]-1,5-BENZOTHIAZEPINES

被引:0
作者
AMBROGI, V
GRANDOLINI, G
PERIOLI, L
GIUSTI, L
LUCACCHINI, A
MARTINI, C
机构
[1] UNIV PERUGIA,IST CHIM FARMACEUT & TECN FARMACEUT,VIA DEL LICEO 1,I-06123 PERUGIA,ITALY
[2] UNIV PISA,IST POLICATTEDRA DISCIPLINE BIOL,I-56100 PISA,ITALY
来源
FARMACO | 1993年 / 48卷 / 05期
关键词
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The 4,5-dihydro-tetrazolo[5, 1-d]-1,5-benzothiazepines 3a-k and the 5-phenyl-s-triazolo[3,4-d]-1,5-benzothiazepines 6a-f and 11a-c have been prepared and tested for their ability to displace [H-3] flunitrazepam binding from bovine brain membranes. Some of the triazoloderivatives showed moderate binding affinity for the benzodiazepine receptor.
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页码:665 / 676
页数:12
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