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The in vitro pharmacology of ZM 241385, a potent, non-xanthine A2a selective adenosine receptor antagonist.

1. This paper describes the in vitro pharmacology of ZM 241385 (4-(2-[7-amino-2-(2-furyl) [1,2,4]-triazolo[2,3-a][1,3,5]triazin- 5-yl amino]ethyl) phenol), a novel non-xanthine adenosine receptor antagonist with selectivity for the A2a receptor subtype. 2. ZM 241385 had high affinity for A2a recepto...

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Bibliografske podrobnosti
Main Authors: Poucher, S. M., Keddie, J. R., Singh, P., Stoggall, S. M., Caulkett, P. W., Jones, G., Coll, M. G.
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1909020/
https://ncbi.nlm.nih.gov/pubmed/7582508
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