SEPARATE BINDING-SITES FOR HISTAMINIC DRUGS IN RAT CEREBRAL-CORTEX

被引：20

作者：

KANDEL, SI ^{[1
]}

STEINBERG, GH ^{[1
]}

WELLS, JW ^{[1
]}

KANDEL, M ^{[1
]}

GORNALL, AG ^{[1
]}

机构：

[1] UNIV TORONTO,DEPT CLIN BIOCHEM,TORONTO M5S 1A1,ONTARIO,CANADA

来源：

BIOCHEMICAL PHARMACOLOGY | 1980年 / 29卷 / 16期

关键词：

D O I：

10.1016/0006-2952(80)90213-0

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：2269 / 2272

页数：4

共 14 条

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SNYDER, SH .

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[6] IMPROMIDINE (SK AND F 92676) IS A VERY POTENT AND SPECIFIC AGONIST FOR HISTAMINE H-2 RECEPTORS [J].

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[7] CHEMICAL DIFFERENTIATION OF HISTAMINE H1-RECEPTOR AND H2-RECEPTOR AGONISTS [J].

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[8] BINDING OF [H-3] MEPYRAMINE TO HISTAMINE H-1 RECEPTORS IN GUINEA-PIG BRAIN [J].

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EMSON, PC ;

YOUNG, JM .

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[9]

HILL SJ, 1979, BRIT J PHARMACOL, V66, pP93

[10] BLOCKADE OF HISTAMINE-INDUCED CONTRACTIONS OF GUINEA-PIG ILEUM BY BETA-HALOALKYLAMINES [J].

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