טוען...
Structure–Activity Relationships of N(6)-Benzyladenosine-5′-uronamides as A(3)-Selective Adenosine Agonists()
Adenosine analogues modified at the 5′-position as uronamides and/or as N(6)-benzyl derivatives were synthesized. These derivatives were examined for affinity in radioligand binding assays at the newly discovered rat brain A(3) adenosine receptor and at rat brain A(1) and A(2a) receptors. 5′-Uronami...
שמור ב:
| הוצא לאור ב: | J Med Chem |
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| Main Authors: | , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
1994
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4474279/ https://ncbi.nlm.nih.gov/pubmed/8126704 |
| תגים: |
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