3,7-DIMETHYL-1-PROPARGYLXANTHINE - A POTENT AND SELECTIVE INVIVO ANTAGONIST OF ADENOSINE-ANALOGS

被引：140

作者：

SEALE, TW

ABLA, KA

SHAMIM, MT

CARNEY, JM

DALY, JW

机构：

[1] UNIV OKLAHOMA,HLTH SCI CTR,DEPT BIOCHEM,OKLAHOMA CITY,OK 73190

[2] UNIV OKLAHOMA,HLTH SCI CTR,DEPT PSYCHIAT,OKLAHOMA CITY,OK 73190

[3] NATL INST DIABET & DIGEST & KIDNEY DIS,BIOORGAN CHEM LAB,BETHESDA,MD 20892

[4] UNIV KENTUCKY,DEPT PHARMACOL,LEXINGTON,KY 40536

来源：

LIFE SCIENCES | 1988年 / 43卷 / 21期

关键词：

D O I：

10.1016/0024-3205(88)90478-X

中图分类号：

R-3 [医学研究方法]; R3 [基础医学];

学科分类号：

1001 ;

摘要：

引用

页码：1671 / 1684

页数：14

共 28 条

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[6] COLLIS MG, 1984, PURINES PHARM PHYSL, P75
[7] STRUCTURE-ACTIVITY-RELATIONSHIPS FOR N6-SUBSTITUTED ADENOSINES AT A BRAIN ADENOSINE-A1-RECEPTOR WITH A COMPARISON TO AN ADENOSINE-A2 RECEPTOR REGULATING CORONARY BLOOD-FLOW
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[8] ANALOGS OF 1,3-DIPROPYL-8-PHENYLXANTHINE - ENHANCEMENT OF SELECTIVITY AT ADENOSINE-A1-RECEPTORS BY ARYL SUBSTITUENTS
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[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1986, 29 (08) : 1520 - 1524
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[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1982, 25 (03) : 197 - 207
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