scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0968-0896(98)00025-X |
P698 | PubMed publication ID | 9681137 |
P50 | author | Christa E Müller | Q30510483 |
Karl-Norbert Klotz | Q42882153 | ||
P2093 | author name string | W Frobenius | |
U Geis | |||
J Sandoval-Ramírez | |||
U Schobert | |||
P2860 | cites work | Molecular cloning and characterization of the human A3 adenosine receptor | Q24564442 |
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3,7-Dimethyl-1-propargylxanthine: a potent and selective in vivo antagonist of adenosine analogs | Q34169391 | ||
The in vitro pharmacology of ZM 241385, a potent, non‐xanthine, A2a selective adenosine receptor antagonist | Q35872902 | ||
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1,3-Dialkyl-8-(p-sulfophenyl)xanthines: potent water-soluble antagonists for A1- and A2-adenosine receptors | Q42204768 | ||
Penetration of adenosine antagonists into mouse brain as determined by ex vivo binding | Q42269942 | ||
Synthesis of paraxanthine analogs (1,7-disubstituted xanthines) and other xanthines unsubstituted at the 3-position: structure-activity relationships at adenosine receptors | Q42286480 | ||
Comparative pharmacology of human adenosine receptor subtypes - characterization of stably transfected receptors in CHO cells. | Q42545166 | ||
Structure-activity relationships of 8-styrylxanthines as A2-selective adenosine antagonists | Q42558334 | ||
Effects of the new A2 adenosine receptor antagonist 8FB-PTP, an 8 substituted pyrazolo-triazolo-pyrimidine, on in vitro functional models | Q42700371 | ||
Solubilities of adenosine antagonists determined by radioreceptor assay | Q45843972 | ||
(E)-1,3-Dialkyl-7-methyl-8-(3,4,5-trimethoxystyryl)xanthines: potent and selective adenosine A2 antagonists | Q46418896 | ||
Synthesis of xanthines as adenosine antagonists, a practical quantitative structure-activity relationship application | Q48467831 | ||
Synthesis and structure-activity relationships of 3,7-dimethyl-1-propargylxanthine derivatives, A2A-selective adenosine receptor antagonists | Q48561677 | ||
Aza-analogs of 8-styrylxanthines as A2A-adenosine receptor antagonists | Q48686852 | ||
Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: potent and selective A(2A) adenosine antagonists | Q49097634 | ||
Configurationally stable analogs of styrylxanthines as A2A adenosine receptor antagonist | Q57708674 | ||
Modulation of erythropoietin production by selective adenosine agonists and antagonists in normal and anemic rats | Q71407634 | ||
In vivo characterisation of ZM 241385, a selective adenosine A2A receptor antagonist | Q71444104 | ||
Photoisomerization of a potent and selective adenosine A2 antagonist, (E)-1,3-Dipropyl-8-(3,4-dimethoxystyryl)-7-methylxanthine | Q72622175 | ||
Solubility of the Xanthines, Antipyrine, and Several Derivatives in Syrup Vehicles | Q72798643 | ||
Adenosine antagonism by purines, pteridines and benzopteridines in human fibroblasts | Q72885800 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 707-719 | |
P577 | publication date | 1998-06-01 | |
P1433 | published in | Bioorganic & Medicinal Chemistry | Q2904200 |
P1476 | title | 8-(Sulfostyryl)xanthines: water-soluble A2A-selective adenosine receptor antagonists | |
P478 | volume | 6 |
Q42577543 | Adenosine A2A receptors in the nucleus accumbens bi-directionally alter cocaine seeking in rats |
Q43503760 | Binding of [3H]MSX-2 (3-(3-hydroxypropyl)-7-methyl-8-(m-methoxystyryl)-1-propargylxanthine) to rat striatal membranes--a new, selective antagonist radioligand for A(2A) adenosine receptors |
Q40169268 | Characterization of the potency, selectivity, and pharmacokinetic profile for six adenosine A2A receptor antagonists |
Q45764150 | Computational studies of the binding modes of A 2A adenosine receptor antagonists |
Q28279556 | Highlights on the development of A(2A) adenosine receptor agonists and antagonists |
Q38768350 | Purinergic A2b Receptor Activation by Extracellular Cues Affects Positioning of the Centrosome and Nucleus and Causes Reduced Cell Migration. |
Q44454321 | Pyrimidin-8-on[2,1-f]theophylline-9-alkylcarboxylic acids amides as A1 and A2A adenosine receptor ligands |
Q40647461 | Recent developments in the field of A2A and A3 adenosine receptor antagonists |
Q45220367 | Receptors subtypes involved in adenosine-mediated modulation of norepinephrine release from cardiac nerve terminals |
Q42321220 | Stimulation of adenosine receptors in the nucleus accumbens reverses the expression of cocaine sensitization and cross-sensitization to dopamine D2 receptors in rats |
Q46729445 | Synthesis and properties of a new water-soluble prodrug of the adenosine A 2A receptor antagonist MSX-2. |
Q34139398 | Xanthines as Adenosine Receptor Antagonists |
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