DEVELOPMENT OF A RADIORECEPTOR ASSAY FOR THE D2-SELECTIVE DOPAMINE AGONIST N-0437

被引：8

作者：

ENSING, K

BLOEMHOF, DA

THOUT, WGI

VANDERLENDE, J

DEZEEUW, RA

机构：

来源：

PHARMACEUTICAL RESEARCH | 1988年 / 5卷 / 05期

关键词：

D O I：

10.1023/A:1015922619831

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

收藏

页码：283 / 287

页数：5

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[1] N,N-DISUBSTITUTED 2-AMINOTETRALINS ARE POTENT D-2 DOPAMINE RECEPTOR AGONISTS
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[4] EVIDENCE FOR ESSENTIAL THIOL-GROUPS AND DISULFIDE BONDS IN AGONIST AND ANTAGONIST BINDING TO THE DOPAMINE RECEPTOR
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[5] INVITRO BINDING OF THE VERY POTENT AND SELECTIVE D-2 DOPAMINE AGONIST, (H-3]N-0437 TO CALF CAUDATE MEMBRANES
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[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1987, 134 (02) : 211 - 219
[6] PHARMACOLOGICAL PROFILES OF 3 NEW, POTENT AND SELECTIVE DOPAMINE RECEPTOR AGONISTS - N-0434, N-0437 AND N-0734
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[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1986, 125 (02) : 273 - 282
[7] REGULATION OF ANTERIOR-PITUITARY D2 DOPAMINE-RECEPTORS BY MAGNESIUM AND SODIUM-IONS
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[J]. JOURNAL OF NEUROCHEMISTRY, 1985, 45 (06) : 1842 - 1849