טוען...
Discovery of A New Human A(2A) Adenosine Receptor Agonist, Truncated 2-Hexynyl-4′-thioadenosine
[Image: see text] The truncated C2- and C8-substituted 4′-thioadenosine derivatives 4a−d were synthesized from d-mannose, using palladium-catalyzed cross-coupling reactions as key steps. In this study, an A(3) adenosine receptor (AR) antagonist, truncated 4′-thioadenosine derivative 3, was successfu...
שמור ב:
| Main Authors: | , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Chemical Society
2010
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| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3030271/ https://ncbi.nlm.nih.gov/pubmed/21286238 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ml1001823 |
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