Selective A1-adenosine receptor antagonists identified using yeast Saccharomyces cerevisiae functional assays
- 1 August 1999
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 9 (16) , 2413-2418
- https://doi.org/10.1016/s0960-894x(99)00398-4
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Derivatives of the Triazoloquinazoline Adenosine Antagonist (CGS 15943) Having High Potency at the Human A2Band A3Receptor SubtypesJournal of Medicinal Chemistry, 1998
- New assay technologies for high-throughput screeningCurrent Opinion in Chemical Biology, 1998
- AdenosinePublished by Elsevier ,1998
- Canine Mast Cell Adenosine Receptors: Cloning and Expression of the A3 Receptor and Evidence that Degranulation Is Mediated by the A2B ReceptorMolecular Pharmacology, 1997
- N6-Cyclopentyl-3‘-substituted-xylofuranosyladenosines: A New Class of Non-Xanthine Adenosine A1 Receptor AntagonistsJournal of Medicinal Chemistry, 1997
- Synthesis and Biological Evaluation of the Enantiomers of the Potent and Selective A1-Adenosine Antagonist 1,3-Dipropyl-8-[2-(5,6-epoxynorbonyl)]- xanthineJournal of Medicinal Chemistry, 1997
- A1-Adenosine receptor antagonistsExpert Opinion on Therapeutic Patents, 1997
- DNA antisense therapy for asthma in an animal modelNature, 1997
- Chiral Pyrrolo[2,3-d]pyrimidine and Pyrimido[4,5-b]indole Derivatives: Structure−Activity Relationships of Potent, Highly Stereoselective A1-Adenosine Receptor Antagonists,Journal of Medicinal Chemistry, 1996
- 7-Deaza-2-phenyladenines: structure-activity relationships of potent A1 selective adenosine receptor antagonistsJournal of Medicinal Chemistry, 1990