18 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
27485602	183	Similarities and differences in affinity and binding modes of tricyclic pyrimido- and pyrazinoxanthines at human and rat adenosine receptors.	Jagiellonian University Medical College
6133953	2	alpha-adrenoreceptor reagents. 1. Synthesis of some 1,4-benzodioxans as selective presynaptic alpha 2-adrenoreceptor antagonists and potential antidepressants.	TBA
20188574	141	2-Amino-5-benzoyl-4-phenylthiazoles: Development of potent and selective adenosine A1 receptor antagonists.	University of Bonn
19569717	251	1-alkyl-8-(piperazine-1-sulfonyl)phenylxanthines: development and characterization of adenosine A2B receptor antagonists and a new radioligand with subnanomolar affinity and subtype specificity.	Institute
12646033	124	Design, synthesis, and biological evaluation of C9- and C2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as new A2A and A3 adenosine receptors antagonists.	Universit£
9667957	5	Nucleosides and nucleotides. 177. 9-(6,7-dideoxy-beta-D-allo-hept-5- ynofuranosyl)adenine: a selective and potent ligand for P3 purinoceptor-like protein.	Hokkaido University
7658429	31	(5aR,11bS)-4,5,5a,6,7,11b-hexahydro-2-propyl-3-thia-5-azacyclopent-1- ena[c]-phenanthrene-9,10-diol (A-86929): a potent and selective dopamine D1 agonist that maintains behavioral efficacy following repeated administration and characterization of its diacetyl prodrug (ABT-431).	Abbott Laboratories
2213824	20	Thiazole as a carbonyl bioisostere. A novel class of highly potent and selective 5-HT3 receptor antagonists.	Pfizer
	44	5-O-Carboxymethyl piperazide derivatives of serotonin: a new class of potent and selective 5-HT1D receptor agonists	TBA
12014951	139	Structure-activity relationships at human and rat A2B adenosine receptors of xanthine derivatives substituted at the 1-, 3-, 7-, and 8-positions.	National Institute of Diabetes & Digestive & Kidney Diseases
30576906	92	Novel non-xanthine antagonist of the A	Bayer Pharmaceuticals
10479303	36	Design, synthesis, and evaluation of chromen-2-ones as potent and selective human dopamine D4 antagonists.	Warner-Lambert
9873377	54	Isoindolinone enantiomers having affinity for the dopamine D4 receptor.	Parke-Davis Pharmaceutical Research
30835463	202	A	Rheinische Friedrich-Wilhelms-Universitat Bonn
9191952	63	Substituted [(4-phenylpiperazinyl)-methyl]benzamides: selective dopamine D4 agonists.	Warner-Lambert
29681156	71	Fluorescent-Labeled Selective Adenosine A	University of Bonn