The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 3346878 |
22 |
8-Aryl-and 8-cycloalkyl-1,3-dipropylxanthines: further potent and selective antagonists for A1-adenosine receptors. |
National Institute of Diabetes, Digestive and Kidney Diseases |
| 27124340 |
10 |
5'-Substituted Amiloride Derivatives as Allosteric Modulators Binding in the Sodium Ion Pocket of the Adenosine A2A Receptor. |
Leiden University |
| 2016708 |
52 |
2-aralkoxyadenosines: potent and selective agonists at the coronary artery A2 adenosine receptor. |
University of South Florida |
| 8355252 |
54 |
Adenosine A1 antagonists. 3. Structure-activity relationships on amelioration against scopolamine- or N6-((R)-phenylisopropyl)adenosine-induced cognitive disturbance. |
Kyowa Hakko Kogyo |
| 1738138 |
62 |
Adenosine receptors: pharmacology, structure-activity relationships, and therapeutic potential. |
Niddk |
| 1619615 |
71 |
2-Alkynyl derivatives of adenosine and adenosine-5'-N-ethyluronamide as selective agonists at A2 adenosine receptors. |
Universit£ |
| 3373486 |
44 |
Adenosine receptor agonists: synthesis and biological evaluation of 1-deaza analogues of adenosine derivatives. |
Universit£ |
| 3351850 |
46 |
125I-labeled 8-phenylxanthine derivatives: antagonist radioligands for adenosine A1 receptors. |
University of Virginia School of Medicine |
| 3018244 |
91 |
N6-substituted N-alkyladenosine-5'-uronamides: bifunctional ligands having recognition groups for A1 and A2 adenosine receptors. |
TBA |
| 15203136 |
39 |
(+/-)8-Amino-5,6,7,8-tetrahydroisoquinolines as novel antinociceptive agents. |
Virginia Commonwealth University |
| | 13 |
Discovery of FK453, a novel non-xanthine adenosine A1 receptor antagonist |
TBA |
| 16458504 |
37 |
Synthesis, in vitro and in vivo evaluation of [O-methyl-11C] 2-{4-[4-(3-methoxyphenyl)piperazin-1-yl]-butyl}-4-methyl-2H-[1,2,4]-triazine-3,5-dione: a novel agonist 5-HT1A receptor PET ligand. |
Columbia University College of Physicians and Surgeons |
| 16392798 |
46 |
Synthesis and in vivo validation of [O-methyl-11C]2-{4-[4-(7-methoxynaphthalen-1-yl)piperazin- 1-yl]butyl}-4-methyl-2H-[1,2,4]triazine-3,5-dione: a novel 5-HT1A receptor agonist positron emission tomography ligand. |
Columbia University College of Physicians and Surgeons |
| 31404862 |
138 |
Imidazopyridine-based selective and multifunctional ligands of biological targets associated with psychiatric and neurodegenerative diseases. |
Palack£ |
| 8496906 |
127 |
Bronchodilator activity of xanthine derivatives substituted with functional groups at the 1- or 7-position. |
Hokuriku University |
| 3172141 |
35 |
Benzo[1,2-c:5,4-c']dipyrazoles: non-xanthine adenosine antagonists. |
Merrell Dow Research Institute |
| 2993622 |
36 |
Functionalized congeners of 1,3-dialkylxanthines: preparation of analogues with high affinity for adenosine receptors. |
TBA |
| 2724296 |
113 |
Effects of 8-phenyl and 8-cycloalkyl substituents on the activity of mono-, di-, and trisubstituted alkylxanthines with substitution at the 1-, 3-, and 7-positions. |
National Institutes of Health |
| 1469687 |
42 |
2-(N'-alkylidenehydrazino)adenosines: potent and selective coronary vasodilators. |
University of South Florida |
| 1404238 |
14 |
7,8-Dihydro-8-ethyl-2-(3-noradamantyl)-4-propyl-1H-imidazo[2,1-i]purin-5(4H)-one: a potent and water-soluble adenosine A1 antagonist. |
Kyowa Hakko Kogyo |
| 1331453 |
106 |
Effects of alkyl substitutions of xanthine skeleton on bronchodilation. |
Hokuriku University |
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