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Volumn 6, Issue 6, 2015, Pages 1178-1185

New selective A2A agonists and A3 antagonists for human adenosine receptors: synthesis, biological activity and molecular docking studies

(8) Rodríguez, Anna a Guerrero, Angel a Gutierrez De Terán, Hugo b Rodríguez, David c Brea, José d Loza, María I d Rosell, Gloria e Pilar Bosch, M a

a INSTITUTE OF ADVANCED CHEMISTRY OF CATALONIA IQAC CSIC (Spain)

b UPPSALA UNIVERSITY (Sweden)

c STOCKHOLM UNIVERSITY (Sweden)

d UNIVERSITY OF SANTIAGO DE COMPOSTELA (Spain)

e UNIVERSITY OF BARCELONA (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE 5' (N ETHYLCARBOXAMIDE); ADENOSINE A1 RECEPTOR; ADENOSINE A2A RECEPTOR; ADENOSINE A2A RECEPTOR AGONIST; ADENOSINE A2B RECEPTOR; ADENOSINE A3 RECEPTOR; ADENOSINE A3 RECEPTOR ANTAGONIST; BENZENE DERIVATIVE; CYCLIC AMP; RADIOLIGAND;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; BIOLOGICAL ACTIVITY; DRUG DETERMINATION; DRUG RECEPTOR BINDING; DRUG STRUCTURE; DRUG SYNTHESIS; EPIMERIZATION; HUMAN; MOLECULAR DOCKING; NONHUMAN; PRIORITY JOURNAL; RECEPTOR BINDING ASSAY; STEREOISOMERISM; STRUCTURE ANALYSIS;

EID: 84935826648 PISSN: 20402503 EISSN: 20402511 Source Type: Journal
DOI: 10.1039/c5md00086f Document Type: Article

Times cited : (10)

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