Fluorenyl derivatives as anti-inflammatory agents
AssigneeScios Nova Inc.
InventorJohn J. Perumattam
Life of this patent
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Abstract
The compound having the formula: ##STR1## and a method of treating an inflammatory condition comprising administering to an animal in need of such treatment an effective amount of at least one compound represented by the formula.
Claims28
A compound having the formula:
- ##STR18## wherein:
- X is selected from the group consisting of methylene, oxygen, ethylene, methyleneoxy, and ethyleneoxy;
- R.sub.1 and R.sub.2 are independently selected from the group consisting of hydrogen, C.sub.1 to C.sub.6 lower alkyl, aryl, aralkyl, alkoxy, alkoxyalkyl, halogen and nitro;
- R.sub.3 is selected from the group consisting of hydrogen and C.sub.1 to C.sub.6 lower alkyl groups;
- R.sub.4 is selected from the group consisting of -CO.sub.2 H;
- -NHSO.sub.2 R.sub.7, wherein R.sub.7 is methyl, or trifluoromethyl;
- -CONHSO.sub.2 R.sub.8, wherein R.sub.8 is methyl, trifluoromethyl, or phenyl;
- 1H-tetrazol-5-yl;
- and -CONH-tetrazol-5-yl;
- R.sub.5 is selected from the group consisting of hydrogen, C.sub.1 to C.sub.6 lower alkyl, halogen, hydroxyl, and a methoxy group;
- and
- R.sub.6 is selected from the group consisting of hydrogen, halogen, C.sub.1 to C.sub.6 lower alkyl, C.sub.1 to C.sub.6 lower alkoxy, C.sub.1 to C.sub.6 lower alkoxy ethers, and alicyclic hydrocarbo groups.
A method of treating an inflammatory condition comprising administering to an animal in need of such treatment an amount of at least one compound represented by the following formula:
- ##STR19## wherein:
- X is selected from the group consisting of methylene, oxygen, ethylene, methyleneoxy, and ethyleneoxy;
- R.sub.1 and R.sub.2 are independently selected from the group consisting of hydrogen, C.sub.1 to C.sub.6 lower alkyl, aryl, aralkyl, alkoxy, alkoxyalkyl, halogen, and nitro;
- R.sub.3 is selected from the group consisting of hydrogen and C.sub.1 to C.sub.6 lower alkyl groups;
- R.sub.4 is selected from the group consisting of -CO.sub.2 H;
- -NHSO.sub.2 R.sub.7, wherein R7 is methyl, or trifluoromethyl;
- -CONHSO.sub.2 R.sub.8, wherein R.sub.8 is methyl, trifluoromethyl, or phenyl;
- 1H-tetrazol-5-yl;
- and -CONH-tetrazol-5-yl;
- R.sub.5 is selected from the group consisting of hydrogen, C.sub.1 to C.sub.6 lower alkyl, halogen, hydroxyl, and a methoxy group;
- and
- R.sub.6 is selected from the group consisting of hydrogen, halogen, C.sub.1 to C.sub.6 lower alkyl, C.sub.1 to C.sub.6 lower alkoxy, C.sub.1 to C.sub.6 lower alkoxy ethers, and alicyclic hydrocarbon groups.
A pharmaceutical composition suitable for use in producing an anti-inflammatory effect in an animal comprising, as an active ingredient, an amount of at least one compound of the following formula administered to an animal together with a pharmaceutically acceptable carrier or diluent ##STR20## wherein:
- X is selected from the group consisting of methylene, oxygen, ethylene, methyleneoxy, and ethyleneoxy;
- R.sub.1 and R.sub.2 are independently selected from the group consisting of hydrogen, C.sub.1 to C.sub.6 lower alkyl, aryl, aralkyl, alkoxy, alkoxyalkyl, halogen, and nitro;
- R.sub.3 is selected from the group consisting of hydrogen, and C.sub.1 to C.sub.6 lower alkyl groups;
- R.sub.4 is selected from the group consisting of -CO.sub.2 H;
- -NHSO.sub.2 R.sub.7, wherein R.sub.7 is methyl, or trifluoromethyl;
- -CONHSO.sub.2 R.sub.8, wherein R.sub.8 is methyl, trifluoromethyl, or phenyl;
- 1H-tetrazol-5-yl;
- and -CONH-tetrazol-5-yl;
- R.sub.5 is selected from the group consisting of hydrogen, C.sub.1 to C.sub.6 lower alkyl, halogen, hydroxyl, and a methoxy group;
- and
- R.sub.6 is selected from the group consisting of hydrogen, halogen, C.sub.1 to C.sub.6 lower alkyl, C.sub.1 to C.sub.6 lower alkoxy, C.sub.1 to C.sub.6 lower alkoxy ethers, and alicyclic hydrocarbo groups.
Dependencies are inferred from the claim text.