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Volumn 444, Issue 3, 2002, Pages 133-141
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KF26777 (2-(4-bromophenyl)-7,8-dihydro-4-propyl-1H-imidazo[2,1-i]purin-5(4H)-one dihydrochloride), a new potent and selective adenosine A3 receptor antagonist
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Author keywords
Adenosine A3 receptor; Binding assay; Ca2+; Guanine nucleotide; KF26777 (2 (4 bromophenyl) 7,8 dihydro 4 propyl 1H imidazo 2,1 i purin 5(4H) one dihydrochloride)
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Indexed keywords
2 (4 BROMOPHENYL) 7,8 DIHYDRO 4 PROPYL 1H IMIDAZO[2,1 I]PURIN 5(4H) ONE;
ADENOSINE A1 RECEPTOR;
ADENOSINE A2A RECEPTOR;
ADENOSINE A2B RECEPTOR;
ADENOSINE A3 RECEPTOR;
ADENOSINE A3 RECEPTOR ANTAGONIST;
ADENOSINE DERIVATIVE;
CALCIUM ION;
DEXAMETHASONE;
GUANOSINE 5' O (3 THIOTRIPHOSPHATE);
KF 26777;
N 6 (4 AMINO 3 IODOBENZYL)ADENOSINE 5' N METHYLURONAMIDE;
UNCLASSIFIED DRUG;
ADENOSINE RECEPTOR;
PURINE DERIVATIVE;
ARTICLE;
CALCIUM CELL LEVEL;
CELL STRAIN HL 60;
CONTROLLED STUDY;
DRUG EFFECT;
DRUG POTENCY;
DRUG RECEPTOR BINDING;
HUMAN;
HUMAN CELL;
PRIORITY JOURNAL;
PROMYELOCYTIC LEUKEMIA;
RECEPTOR UPREGULATION;
ANIMAL;
CELL LINE;
CHO CELL;
DRUG ANTAGONISM;
HAMSTER;
METABOLISM;
ANIMAL;
CELL LINE;
CHO CELLS;
HAMSTERS;
HL-60 CELLS;
HUMAN;
PURINES;
RECEPTORS, PURINERGIC P1;
ANIMALS;
CRICETINAE;
HUMANS;
RECEPTOR, ADENOSINE A3;
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EID: 0037204734
PISSN: 00142999
EISSN: None
Source Type: Journal
DOI: 10.1016/S0014-2999(02)01662-X Document Type: Article |
Times cited : (29)
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References (51)
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