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• W1992080487 abstract "In the last few years, many efforts have been made to search for potent and selective human A3 adenosine antagonists. In particular, one of the most promising human A3 adenosine receptor antagonists is represented by the pyrazolo-triazolo-pyrimidine family. This class of compounds has been strongly investigated from the point of view of structure-activity relationships. In particular, it has been observed that fundamental requisites for having both potency and selectivity at the human A3 adenosine receptors are the presence of a small substituent at the N8 position and an unsubstitued phenyl carbamoyl moiety at the N5 position. In this study, we report the role of the N5-bond type on the affinity and selectivity at the four adenosine receptor subtypes. The observed structure-activity relationships of this class of antagonists are also exhaustively rationalized using the recently published ligand-based homology modeling approach." @default.
• W1992080487 created "2016-06-24" @default.
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• W1992080487 date "2007-07-25" @default.
• W1992080487 modified "2023-10-15" @default.
• W1992080487 title "Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes" @default.
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• W1992080487 doi "https://doi.org/10.1007/s11302-007-9058-y" @default.
• W1992080487 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2245997" @default.
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