N6-CYCLOALKYLADENOSINES - POTENT, A1-SELECTIVE ADENOSINE AGONISTS

被引：125

作者：

MOOS, WH ^{[1
]}

SZOTEK, DS ^{[1
]}

BRUNS, RF ^{[1
]}

机构：

[1] WARNER LAMBERT PARKE DAVIS,PHARMACEUT RES,DEPT PHARMACOL,ANN ARBOR,MI 48105

来源：

JOURNAL OF MEDICINAL CHEMISTRY | 1985年 / 28卷 / 10期

关键词：

D O I：

10.1021/jm00148a001

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

引用

页码：1383 / 1384

页数：2

共 14 条

[1]

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[3]

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[4]

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[9] INHIBITORY-ACTION OF ADENOSINE AND ADENOSINE-ANALOGS ON NEUROTRANSMISSION IN THE OLFACTORY CORTEX SLICE OF GUINEA-PIG - STRUCTURE-ACTIVITY-RELATIONSHIPS [J].

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[10] MODIFICATION OF THE 5' POSITION OF PURINE NUCLEOSIDES .2. SYNTHESIS AND SOME CARDIOVASCULAR PROPERTIES OF ADENOSINE-5'-(N-SUBSTITUTED)CARBOXAMIDES [J].

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