N-0437 - A SELECTIVE D-2 DOPAMINE RECEPTOR AGONIST IN INVITRO AND INVIVO MODELS

被引：45

作者：

VANDERWEIDE, J

DEVRIES, JB

TEPPER, PG

KRAUSE, DN

DUBOCOVICH, ML

HORN, AS

机构：

[1] STATE UNIV GRONINGEN,DEPT MED CHEM,ANTONIUS DEUSINGLAAN 2,9713 AW GRONINGEN,NETHERLANDS

[2] NELSON RES & DEV CO,DEPT MOLEC PHARMACOL,IRVINE,CA 92715

[3] NORTHWESTERN UNIV,SCH MED,DEPT PHARMACOL,CHICAGO,IL 60611

来源：

EUROPEAN JOURNAL OF PHARMACOLOGY | 1988年 / 147卷 / 02期

关键词：

D O I：

10.1016/0014-2999(88)90783-2

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：249 / 258

页数：10

共 39 条

[1] N,N-DISUBSTITUTED 2-AMINOTETRALINS ARE POTENT D-2 DOPAMINE RECEPTOR AGONISTS
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[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1984, 105 (1-2) : 15 - 21
[2] CHARACTERISTICS OF GABAB RECEPTOR-BINDING SITES ON RAT WHOLE BRAIN SYNAPTIC-MEMBRANES
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HILL, DR
HUDSON, AL
[J]. BRITISH JOURNAL OF PHARMACOLOGY, 1983, 78 (01) : 191 - 206
[3] BRADBURY AJ, 1982, ADV BIOSCI, V37, P413
[4] ADENOSINE RECEPTORS IN BRAIN MEMBRANES - BINDING OF N6-CYCLOHEXYL[H-3]ADENOSINE AND 1,3-DIETHYL-8-[H-3]PHENYLXANTHINE
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DALY, JW
SNYDER, SH
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (09): : 5547 - 5551
[5] BYLUND DB, 1976, MOL PHARMACOL, V12, P568
[6] CHARACTERIZATION OF THE MECHANISMS BY WHICH PURPORTED DOPAMINE AGONISTS REDUCE SPONTANEOUS LOCOMOTOR-ACTIVITY OF MICE
COSTALL, B
LIM, SK
NAYLOR, RJ
[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1981, 73 (2-3) : 175 - 188
[7] SIMILARITIES BETWEEN NEUROLOGIC EFFECTS OF L-DOPA AND OF APOMORPHINE
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[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1970, 282 (01) : 31 - +
[8] DUBOCOVICH ML, 1985, J PHARMACOL EXP THER, V234, P395
[9] IS TL-99 A SELECTIVE PRE-SYNAPTIC DOPAMINE RECEPTOR AGONIST
HORN, AS
DEVRIES, J
DIJKSTRA, D
MULDER, AH
[J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1982, 83 (1-2) : 35 - 45
[10] SYNTHESIS AND RADIORECEPTOR BINDING-ACTIVITY OF N-0437, A NEW, EXTREMELY POTENT AND SELECTIVE D2 DOPAMINE RECEPTOR AGONIST
HORN, AS
TEPPER, P
VANDERWEIDE, J
WATANABE, M
GRIGORIADIS, D
SEEMAN, P
[J]. PHARMACEUTISCH WEEKBLAD-SCIENTIFIC EDITION, 1985, 7 (05) : 208 - 211

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