ANALOGS OF CAFFEINE - ANTAGONISTS WITH SELECTIVITY FOR A2 ADENOSINE RECEPTORS

被引:95
作者
UKENA, D
SHAMIM, MT
PADGETT, W
DALY, JW
机构
关键词
D O I
10.1016/0024-3205(86)90023-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
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页码:743 / 750
页数:8
相关论文
共 15 条
[1]   ADENOSINE RECEPTOR-BINDING - STRUCTURE-ACTIVITY ANALYSIS GENERATES EXTREMELY POTENT XANTHINE ANTAGONISTS [J].
BRUNS, RF ;
DALY, JW ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (07) :2077-2080
[2]   ADENOSINE RECEPTORS IN BRAIN MEMBRANES - BINDING OF N6-CYCLOHEXYL[H-3]ADENOSINE AND 1,3-DIETHYL-8-[H-3]PHENYLXANTHINE [J].
BRUNS, RF ;
DALY, JW ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (09) :5547-5551
[3]  
COLLIS MG, PURINES PHARM PHYSL, P75
[4]   8-PHENYLTHEOPHYLLINE POTENTIATES THE ELECTRICAL-ACTIVITY EVOKED IN HIPPOCAMPAL SLICES [J].
CORRADETTI, R ;
MORONI, F ;
PASSANI, MB ;
PEPEU, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1984, 103 (1-2) :177-180
[5]   5'-N-ETHYLCARBOXAMIDOADENOSINE - A POTENT INHIBITOR OF HUMAN-PLATELET AGGREGATION [J].
CUSACK, NJ ;
HOURANI, SMO .
BRITISH JOURNAL OF PHARMACOLOGY, 1981, 72 (03) :443-447
[6]   1,3-DIALKYL-8-(PARA-SULFOPHENYL)XANTHINES - POTENT WATER-SOLUBLE ANTAGONISTS FOR A1-ADENOSINE AND A2-ADENOSINE RECEPTORS [J].
DALY, JW ;
PADGETT, W ;
SHAMIM, MT ;
BUTTSLAMB, P ;
WATERS, J .
JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (04) :487-492
[7]   ADENOSINE RECEPTORS - TARGETS FOR FUTURE DRUGS [J].
DALY, JW .
JOURNAL OF MEDICINAL CHEMISTRY, 1982, 25 (03) :197-207
[8]  
DALY JW, 1986, J MED CHEM
[9]   THE ACTION OF ADENOSINE-ANALOGS ON PC12 CELLS [J].
GUROFF, G ;
DICKENS, G ;
END, D ;
LONDOS, C .
JOURNAL OF NEUROCHEMISTRY, 1981, 37 (06) :1431-1439
[10]   FUNCTIONALIZED CONGENERS OF ADENOSINE - PREPARATION OF ANALOGS WITH HIGH-AFFINITY FOR A1-ADENOSINE RECEPTORS [J].
JACOBSON, KA ;
KIRK, KL ;
PADGETT, WL ;
DALY, JW .
JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (09) :1341-1346