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Volumn 61, Issue 2, 2002, Pages 415-424
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A3 adenosine receptors in human neutrophils and promyelocytic HL60 cells: A pharmacological and biochemical study
a,b a,b a,b a,b a,b c a a,b |
Author keywords
[No Author keywords available]
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Indexed keywords
2 (2 FURYL) 5 [3 (4 METHOXYPHENYL)UREIDO] 8 PROPYLPYRAZOLO[4,3 E] 1,2,4 TRIAZOLO[1,5 C]PYRIMIDINE;
5 N (4 METHOXYPHENYLCARBAMOYL)AMINO 8 PROPYL 2 (2 FURYL)PYRAZOLO[4,3 E] 1,2,4 TRIAZOLO[1,5 C]PYRIMIDINE;
ADENOSINE A3 RECEPTOR ANTAGONIST;
ADENOSINE RECEPTOR AFFECTING AGENT;
PYRIMIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
BINDING AFFINITY;
BINDING SITE;
DRUG RECEPTOR BINDING;
HUMAN;
HUMAN CELL;
LIGAND BINDING;
NEUTROPHIL;
PRIORITY JOURNAL;
PROMYELOCYTIC LEUKEMIA;
REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;
ADENOSINE;
BINDING, COMPETITIVE;
BIOLOGICAL TRANSPORT;
CALCIUM;
CYCLIC AMP;
GENE EXPRESSION;
GRANULOCYTES;
HL-60 CELLS;
HUMANS;
NEUTROPHILS;
PHENYLUREA COMPOUNDS;
RECEPTOR, ADENOSINE A3;
RECEPTORS, PURINERGIC P1;
SUPEROXIDES;
TRIAZOLES;
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EID: 0036156443
PISSN: 0026895X
EISSN: None
Source Type: Journal
DOI: 10.1124/mol.61.2.415 Document Type: Article |
Times cited : (112)
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References (40)
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