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. 1983 Apr;80(7):2077–2080. doi: 10.1073/pnas.80.7.2077

Adenosine receptor binding: structure-activity analysis generates extremely potent xanthine antagonists.

R F Bruns, J W Daly, S H Snyder
PMCID: PMC393756  PMID: 6300892

Abstract

Structure-activity analysis of alkylxanthine derivatives at adenosine receptor binding sites has been employed to design more potent adenosine receptor antagonists. Receptor affinities of xanthines were determined by measuring inhibition of the binding of N6-[3H]cyclohexyladenosine to bovine brain membranes. 1,3-Dipropyl substitutions enhance potency compared to the 1,3-dimethyl substitution in theophylline. An 8-phenyl substituent produces a considerable increase in potency, which is augmented by certain para substitutions on the 8-phenyl ring. Combining an ortho amino with a para-chloro substituent on the 8-phenyl ring affords further increases in potency. Combining all of these substituents results in 1,3-dipropyl-8-(2-amino-4-chlorophenyl) xanthine, a compound of extraordinary receptor affinity, with a Ki for adenosine A1 receptors of 22 pM. It is 4,000,000 times more potent than xanthine itself and 70,000 times more potent than theophylline.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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