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Xanthine Functionalized Congeners as Potent Ligands at A(2)-Adenosine Receptors(,)
Amide derivatives of a carboxylic acid congener of 1,3-dialkylxanthine, having a 4-[(carboxymethyl)oxy]phenyl substituent at the 8-position, have been synthesized in order to identify potent antagonists at A(2)-adenosine receptors stimulatory to adenylate cyclase in platelets. Distal structural feat...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
1987
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3433718/ https://ncbi.nlm.nih.gov/pubmed/3806597 |
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