6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-one cGMP-PDE inhibitors for the treatment of erectile dysfunction
AssigneePfizer Inc.
InventorsSimon Fraser Campbell, Alexander Roderick Mackenzie, Anthony Wood
Life of this patent
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Abstract
6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-one compounds which are selective inhibitors of cGMP PDE are useful in the treatment of erectile dysfunction (impotence) in male animals, including man.
Claims7
The use of a compound which is a selective cGMP PDE inhibitor for the manufacture of a medicament for the treatment of erectile dysfunction in a male animal, including man, wherein said compound is:
- i a 5-substituted pyrazolo [4,3-d]pyrimdine-7-one as disclosed in European patent application 0201188;
- ii a griseolic acid derivative as disclosed in European patent applications nos 0214708 and 0319050;
- iii a 2-phenylpurinone derivative as disclosed in European patent application 0293063;
- iv a phenylpyridone derivative as disclosed in European patent application 0347027;
- v a fused pyrimidine derivative as disclosed in European patent application 0347146;
- vi a condensed pyrimidine derivative as disclosed in European patent application 0349239;
- vii a pyrimidopyrimidine derivative as disclosed in European patent application 0351058;
- viii a purine compound as disclosed in European patent application 0352960;
- ix a quinazolinone derivative as disclosed in European patent application 0371731;
- x a phenylpyrimidone derivative as disclosed in European patent application 0395328;
- xi an imidazoquinoxalinone derivative or its aza analogue as disclosed in European patent application 0400583;
- xii a phenylpyrimidone derivative as disclosed in European patent application 0400799;
- xiii a phenylpyridone derivative as disclosed in European patent application 0428268;
- xiv a pyrimidopyrimidine derivative as disclosed in European patent 0442204;
- xv a 4-aminoquinazoline derivative as disclosed in European patent application 0579496;
- xvi a 4,5-dihydro-4-oxo-pyrrolo[1,2-a]quinoxaline derivative or its aza analogue as disclosed in European patent application 0584487;
- xvii a polycyclic guanine derivative as disclosed in International patent application WO91/19717;
- xviii a nitrogenous heterocyclic compound as disclosed in International patent application WO93/07124;
- xix a 2-benzyl-polycyclic guanine derivative as disclosed in International patent application WO94/19351;
- xx a quinazoline derivative as disclosed in U.S. Pat. No. 4,060,615
- xxi a 6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-one as disclosed in U.S. Pat. No. 5,294,612
- xxii a benzimidazole as disclosed in Japanese patent application 5-222000;
- or
- xxiii a cycloheptimidazole as disclosed in European Journal of Pharmacology, 251, (1994),1.
- xxiv a N-containing heterocycle as disclosed in International patent application WO94/22855.
The use of a compound which is a selective cGMP PDE inhibitor for the manufacture of a medicament for the treatment of erectile dysfunction in a male animal, including man, wherein said compound is:
- xxv a pyrazolopyrimidine derivative as disclosed in European patent application 0636626;
- xxvi a 4-aminopyrimidine derivative as disclosed in European patent application 0640599;
- xxvii a imidazoquinazoline derivative as disclosed in International patent application WO95/06648;
- xxviii an anthranilic acid derivative as disclosed in International patent application WO095/18097;
- xxix a 4-aminoquinazoline derivative as disclosed in U.S. Pat. No. 5,436,233;
- xxx a tetracyclic derivative as disclosed in International patent application WO95/19978;
- xxxi a imidazoquinazoline derivative as disclosed in European patent application 0668280;
- or
- xxxii a quinazoline compound as disclosed in European patent application 0669324.
Dependencies are inferred from the claim text.