Indexed keywords
2 (2 FURYL) 5 [3 (4 METHOXYPHENYL)UREIDO] 8 PROPYLPYRAZOLO[4,3 E] 1,2,4 TRIAZOLO[1,5 C]PYRIMIDINE;
2 [4 (2 CARBOXYETHYL)PHENETHYLAMINO]ADENOSINE 5' (N ETHYLCARBOXAMIDE);
5 AMINO 2 (2 FURYL) 7 (2 PHENYLETHYL)PYRAZOLO[4,3 E][1,2,4]TRIAZOLO[1,5 C]PYRIMIDINE;
5N (3 CHLOROPHENYLCARBAMOYL)AMINO 8 PROPYL 2 (2 FURYL)PYRAZOLO[4,3 E] 1,2,4 TRIAZOLO[1,5 C]PYRIMIDINE;
5N (4 METHOXYPHENYLCARBAMOYL)AMINO 8 PROPYL 2 (2 FURYL)PYRAZOLO[4,3 E] 1,2,4 TRIAZOLO[1,5 C]PYRIMIDINE;
8 CYCLOPENTYL 1,3 DIPROPYLXANTHINE;
9 CHLORO 2 (2 FURYL) 5,6 DIHYDRO 5 IMINO 1,2,4 TRIAZOLO[2,3 C]QUINAZOLINE;
ADENOSINE 5' (N ETHYLCARBOXAMIDE);
ADENOSINE 5' (N METHYLCARBOXAMIDE);
ADENOSINE A3 RECEPTOR;
ADENOSINE RECEPTOR BLOCKING AGENT;
ADENOSINE RECEPTOR STIMULATING AGENT;
CYCLIC AMP;
IODINE 125;
LIGAND;
MRE 3010F20;
PHENYLISOPROPYLADENOSINE;
RECEPTOR SUBTYPE;
TRITIUM;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ARTICLE;
BINDING AFFINITY;
CHO CELL;
DRUG RECEPTOR BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
ISOTOPE LABELING;
NONHUMAN;
PRIORITY JOURNAL;
ADENOSINE;
ADENYLATE CYCLASE;
ANIMALS;
BINDING, COMPETITIVE;
CHO CELLS;
CRICETINAE;
CYCLIC AMP;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HUMANS;
PHENYLUREA COMPOUNDS;
RADIOLIGAND ASSAY;
RATS;
RECEPTOR, ADENOSINE A3;
RECEPTORS, PURINERGIC P1;
TRIAZOLES;
TRITIUM;
1
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