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Structure–Activity Relationships of 8-Styrylxanthines as A(2)-Selective Adenosine Antagonists(,)
A series of substituted 8-styryl derivatives of 1,3,7-alkylxanthines was synthesized as potential A(2)-selective adenosine receptor antagonists, and the potency at rat brain A(1)- and A(2)-receptors was studied in radioligand binding experiments. At the xanthine 7-position, only small hydrophobic su...
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| Vydáno v: | J Med Chem |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
1993
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5975975/ https://ncbi.nlm.nih.gov/pubmed/8496902 |
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