8-(Sulfostyryl)xanthines: water-soluble A2A-selective adenosine receptor antagonists.

Bioorg Med Chem

Institut für Pharmazie und Lebensmittelchemie, Julius-Maximilians-Universität Würzburg, Pharmazeutische Chemie, Germany.

Published: June 1998

8-(Sulfostyryl)xanthine derivatives were synthesized as water-soluble A2A-selective adenosine receptor (AR) antagonists. meta- and para-sulfostyryl-DMPX (3,7-dimethyl-1-propargylxanthine) derivatives 11a and 11b exhibited high affinity to rat A2A-AR in submicromolar concentrations, and were 20- to 30-fold selective versus rat A1-AR. Styryl-DMPX derivatives were inactive at human A2B- and A3-AR. 1,3-Dipropyl-8-p-sulfostyrylxanthine (13) or only a 7-methyl derivative (14) showed similar (13) or higher (14) A2A affinity than 11a and 11b but showed no (13) or only a low degree (14) of selectivity versus A1-, A2B-, and A3-AR. The A2A-selective sulfostyryl-DMPX derivatives exhibit high water-solubility and may be useful research tools for in vivo studies.

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0968-0896(98)00025-xDOI Listing

Publication Analysis

Top Keywords

water-soluble a2a-selective
8
a2a-selective adenosine
8
adenosine receptor
8
receptor antagonists
8
11a 11b
8
a2b- a3-ar
8
8-sulfostyrylxanthines water-soluble
4
antagonists 8-sulfostyrylxanthine
4
derivatives
4
8-sulfostyrylxanthine derivatives
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!