QUANTITATIVE COMPARISON OF BROMOACETYLATED DERIVATIVES OF ALPRENOLOL AND PINDOLOL ON BETA-ADRENERGIC-RECEPTOR BINDING AND MOBILITY IN S49-CELLS

被引：1

作者：

BOX, RJ ^{[1
]}

机构：

[1] KANTONSSPITAL,DEPT FORSCH,CH-4031 BASEL,SWITZERLAND

来源：

JOURNAL OF RECEPTOR RESEARCH | 1989年 / 9卷 / 4-5期

关键词：

D O I：

10.3109/10799898909066065

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

引用

页码：385 / 403

页数：19

共 19 条

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[7] DETERMINATION OF THE DESENSITIZATION OF BETA-ADRENERGIC RECEPTORS BY [H-3]-LABELED CGP-12177
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[J]. BIOCHEMICAL JOURNAL, 1983, 216 (03) : 669 - 674
[8] IRREVERSIBLE BLOCKADE OF BETA-ADRENERGIC RECEPTORS WITH A BROMOACETYL DERIVATIVE OF PINDOLOL
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[J]. NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1985, 328 (03) : 279 - 287
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[10] SHAPE CHANGE AND UPTAKE OF 5-HYDROXYTRYPTAMINE IN HUMAN-BLOOD PLATELETS - ACTION OF NEUROPSYCHOTROPIC DRUGS
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[J]. LIFE SCIENCES, 1979, 24 (20) : 1833 - 1840

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