The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 2016708 |
52 |
2-aralkoxyadenosines: potent and selective agonists at the coronary artery A2 adenosine receptor. |
University of South Florida |
| 17933541 |
145 |
5'-Carbamoyl derivatives of 2'-C-methyl-purine nucleosides as selective A1 adenosine receptor agonists: affinity, efficacy, and selectivity for A1 receptor from different species. |
Universit£ |
| 8246243 |
9 |
Photoisomerization of a potent and selective adenosine A2 antagonist, (E)-1,3-Dipropyl-8-(3,4-dimethoxystyryl)-7-methylxanthine. |
Kyowa Hakko Kogyo |
| 8355252 |
54 |
Adenosine A1 antagonists. 3. Structure-activity relationships on amelioration against scopolamine- or N6-((R)-phenylisopropyl)adenosine-induced cognitive disturbance. |
Kyowa Hakko Kogyo |
| 1548682 |
126 |
8-Polycycloalkyl-1,3-dipropylxanthines as potent and selective antagonists for A1-adenosine receptors. |
Kyowa Hakko Kogyo |
| 1738138 |
62 |
Adenosine receptors: pharmacology, structure-activity relationships, and therapeutic potential. |
Niddk |
| 1469688 |
31 |
2-(N'-aralkylidenehydrazino)adenosines: potent and selective coronary vasodilators. |
University of South Florida |
| 1501234 |
111 |
Adenosine A1 antagonists. 2. Structure-activity relationships on diuretic activities and protective effects against acute renal failure. |
Kyowa Hakko Kogyo |
| 2016707 |
34 |
2-Alkoxyadenosines: potent and selective agonists at the coronary artery A2 adenosine receptor. |
University of South Florida |
| 15203164 |
38 |
Structure-affinity relationships of 5'-aromatic ethers and 5'-aromatic sulfides as partial A1 adenosine agonists, potential supraventricular anti-arrhythmic agents. |
Cv Therapeutics |
| 10714510 |
36 |
The discovery and synthesis of highly potent, A2a receptor agonists. |
Glaxowellcome Medicines Research Centre |
| | 52 |
Adenosine A2A antagonists with potent anti-cataleptic activity |
TBA |
| | 13 |
Discovery of FK453, a novel non-xanthine adenosine A1 receptor antagonist |
TBA |
| 9191953 |
11 |
Synthesis and biological evaluation of the enantiomers of the potent and selective A1-adenosine antagonist 1,3-dipropyl-8-[2-(5,6-epoxynorbonyl)]-xanthine. |
Cv Therapeutics |
| 8809156 |
2 |
Synthesis and cardiotonic activity of novel pyrimidine derivatives: crystallographic and quantum chemical studies. |
Università |
| 8496906 |
127 |
Bronchodilator activity of xanthine derivatives substituted with functional groups at the 1- or 7-position. |
Hokuriku University |
| 1992150 |
60 |
8-(Dicyclopropylmethyl)-1,3-dipropylxanthine: a potent and selective adenosine A1 antagonist with renal protective and diuretic activities. |
Kyowa Hakko Kogyo |
| 1613758 |
95 |
(E)-1,3-dialkyl-7-methyl-8-(3,4,5-trimethoxystyryl)xanthines: potent and selective adenosine A2 antagonists. |
Kyowa Hakko Kogyo |
| 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 |
| 25590533 |
245 |
Identification of a fragment-like small molecule ligand for the methyl-lysine binding protein, 53BP1. |
University of North Carolina At Chapel Hill |
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