Synthesis of a series of new 2-phenyl-9-benzyl-8-azaadenines bearing on N6 an alkyl or aralkyl chain having a carbonyloxymethyl group on the carbon bound to N6 were reported. The ester group could assure to the molecule a better water-solubility than the 8-azaadenines 2, 6 and 9 substituted with lipophilic groups synthesised in the past. Compounds synthesised demonstrated only little capability of binding A1 adenosine receptors.

NEW 2-(2'-PHENYL-9'-AZAPURIN-6'-YLAMINO)-CARBOXYLIC ACID METHYLESTERS AS LIGANDS FOR A1 ADENOSINE RECEPTORS

GIORGI, IRENE;
2001-01-01

Abstract

Synthesis of a series of new 2-phenyl-9-benzyl-8-azaadenines bearing on N6 an alkyl or aralkyl chain having a carbonyloxymethyl group on the carbon bound to N6 were reported. The ester group could assure to the molecule a better water-solubility than the 8-azaadenines 2, 6 and 9 substituted with lipophilic groups synthesised in the past. Compounds synthesised demonstrated only little capability of binding A1 adenosine receptors.
2001
Biagi, G; Giorgi, Irene; F., Pacchini; O., Livi; V., Scartoni
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/176999
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