Pro-drugs of adenosine receptor agonists
The invention relates to a method of improving oral drug absorption of adenosine analogues by the use of 2′-methoxy adenosine pro-drugs and to the use of these pro-drugs as medicaments. The invention further relates to compounds that are pro-drugs of adenosine receptor agonists, and to their use as therapeutic compounds, in particular as analgesic or anti-inflammatory compounds, or as disease modifying antirheumatic drugs (DMARDs), and to methods of preventing, treating or ameliorating pain or inflammation using these compounds.
1. A compound selected from:
(2R,3R,4R,5R)-5[6-amino-2-(cyclopentylmethoxy)-9H-purin-9-yl]-2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol;
(2R,3R,4R,5R)-5-{6-amino-2-[(2,2,3,3-tetrafluorocyclobutyl)oxy]-9H-purin-9-yl}-2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol;
(2R,3R,4R,5R)-5[6-amino-2-(2,5-difluorophenoxy)-9H-purin-9-yl]-2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol;
(2R,3R,4R,5R)-5[6-amino-2-(3,4-difluorophenoxy)-9H-purin-9-yl]-2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol;
(2R,3R,4R,5R)-5[6-amino-2[4-chloro-3-(trifluoromethyl)phenoxy]-9H-purin-9-yl]-2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol;
(2R,3R,4R,5R)-5-(6-amino-2-{[(1S)-1-methylpropyl]amino}-9H-purin-9-yl)- 2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol; and
(2R,3R,4R,5R)-5-[6-amino-2-(cyclohexylamino)-9H-purin-9-yl]-2-(hydroxymethyl)-4-methoxytetrahydrofuran-3-ol.
2. A pharmaceutical formulation containing a compound according to claim 1 as active ingredient, in combination with a pharmaceutically acceptable carrier, excipient, or diluent.
3. A pharmaceutical formulation according to claim 2 further comprising an additional therapeutic agent for use in the treatment or amelioration of a pathological condition that can be improved by agonism of adenosine A2A receptors.
4. The pharmaceutical formulation according to claim 3 wherein the additional therapeutic agent is useful for treating pain, inflammation and/or arthropathy.
5. A method for the treatment or amelioration of a pathological condition that can be improved by agonism of adenosine A2A receptors in a subject comprising administering to the subject an effective amount of a compound according to claim 1 , wherein said pathological condition is neuropathic pain.