Claims
- 1. A method for treating a patient with an autoimmune or inflammatory disease which method comprises administering to said patient a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an effective autoimmune or inflammatory disease-treating amount of a compound of formula I: ##STR10## wherein R.sup.1 is selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, aralkyl, aryl, cycloalkyl, cycloalkylalkyl and cycloalkenyl;
- each R.sup.2 is independently selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, aralkyl, aryl, alkoxy, substituted alkoxy, cycloalkyl and halo;
- R.sup.3 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, aralkyl, aryl, cycloalkyl and cycloalkyalkyl;
- R.sup.4 is selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, aralkyl, aryl, cycloalkyl, cycloalkylalkyl and cycloalkenyl; and n is an integer ranging from 0 to 2; and optical isomers and racemates thereof, and pharmaceutically acceptable salts thereof.
- 2. The method according to claim 1 wherein the autoimmune disease is systemic lupus or multiple sclerosis.
- 3. The method according to claim 1 wherein the inflammatory disease is rheumatoid arthritis, septic shock, erythema nodosum leprosy, septicemia, uveitis, adult respiratory distress syndrome, or inflammatory bowel disease.
- 4. The method of claim 1 wherein n is 0.
- 5. The method of claim 4 wherein R.sup.3 is hydrogen.
- 6. The method of claim 5 wherein R.sup.1 is a substituted phenyl group having the formula: ##STR11## wherein each R.sup.5 is independently selected from the group consisting of alkyl, substituted alkyl, cycloalkyl, aralkyl, aryl, alkoxy, substituted alkoxy, aryloxy, aralkyloxy, cycloalkoxy, acyl, acylamino, aminocarbonyl, alkoxycarbonyl, carboxyl, cyano, halo, hydroxy, nitro, sulfonate, thioalkoxy, and --NR.sup.6 R.sup.7, where R.sup.6 and R.sup.7 are each independently selected from hydrogen, alkyl, substituted alkyl or aryl; or two adjacent R.sup.5 groups can be joined together to form an alkylene or alkylenedioxy group; and
- m is an integer from 1 to 5.
- 7. The method of claim 6 wherein R.sup.5 is selected from the group consisting of alkyl, alkoxy, substituted alkoxy, acylamino, thioalkoxy.
- 8. The method of claim 7 wherein R.sup.5 is a methyl, methoxy, trifluoromethoxy, acetamido or thiomethoxy group and m is 1 or 2.
- 9. The method of claim 5 wherein R.sup.1 is selected from the group consisting of 2-methoxyphenyl, 4-methoxyphenyl, 4-trifluoromethoxyphenyl, 3,5-dimethylphenyl, 4-acetamidophenyl and 4-thiomethoxyphenyl.
- 10. The method of claim 4 wherein R.sup.4 is selected from the group consisting of alkyl, substituted alkyl, aralkyl, cycloalkyl and cycloalkylalkyl.
- 11. The method of claim 10 wherein R.sup.4 is alkyl or cycloalkyl.
- 12. The method of claim 11 wherein R.sup.4 is selected from the group consisting of n-propyl, isopropyl, tert-butyl, cyclopentyl, cyclohexyl and 2,4,4-trimethypent-2-yl.
- 13. The method of claim 1 wherein the compound of formula I is selected from a compound of formula II: ##STR12## wherein each R.sup.8 is independently selected from the group consisting of alkyl, alkoxy, acylamino, trifluoromethoxy and thioalkoxy;
- R.sup.9 is selected from the group consisting of alkyl and cycloalkyl; and
- p is an integer ranging from 1 to 3;
- and optical isomers and racemates thereof, and pharmaceutically acceptable salts thereof.
- 14. The method of claim 13 wherein R.sup.8 is a methyl, methoxy, trifluoromethoxy, acetamido or thiomethoxy group and p is 1 or 2.
- 15. The method of claim 13 wherein R.sup.9 is n-propyl, isopropyl, tert-butyl, cyclopentyl, cyclohexyl or 2,4,4-trimethylpent-2-yl.
- 16. The method of claim 1 wherein the compound of formula I is selected from:
- .alpha.-[2-(4-methoxyphenylthio)-5-furyl]-N-tert-butylnitrone,
- .alpha.-[2-(2-methoxyphenylthio)-5-furyl]-N-tert-butylnitrone,
- .alpha.-[2-(4-methoxyphenylthio)-5-furyl]-N-cyclohexylnitrone,
- .alpha.-[2-(4-trifluoromethoxyphenylthio)-5-furyl]-N-tert-butylnitrone,
- .alpha.-[2-(3,5-dimethylphenylthio)-5-furyl]-N-tert-butylnitrone,
- .alpha.-[2-(4-acetamidophenylthio)-5-furyl]-N-tert-butylnitrone,
- .alpha.-[2-(4-ethylphenylthio)-5-furyl]-N-tert-butylnitrone,
- .alpha.-[2-(4-thiomethoxyphenylthio)-5-furyl]-N-tert-butylnitrone,
- .alpha.-[2-(4-methoxyphenylthio)-5-furyl]-N-isopropylnitrone,
- .alpha.-[2-(4-trifluoromethoxyphenylthio)-5-furyl]-N-cyclohexylnitrone,
- .alpha.-[2-(4-methoxyphenylthio)-5-furyl]-N-n-butylnitrone,
- .alpha.-[2-(4-methoxyphenylthio)-5-furyl]-N-n-propylnitrone,
- .alpha.-[2-(4-trifluoromethoxyphenylthio)-5-furyl]-N-isopropylnitrone,
- .alpha.-[2-(4-trifluoromethoxyphenylthio)-5-furyl]-N-n-propylnitrone,
- .alpha.-[2-(4-methoxyphenylthio)-5-furyl]-N-2,4,4-trimethylpent-2-ylnitrone
- .alpha.-[2-(4-trifluoromethoxyphenylthio)-5-furyl]-N-2,4,4-trimethylpent-2-ylnitrone,
- .alpha.-[2-(4-methoxyphenylthio)-5-furyl]-N-cyclopentylnitrone, and
- .alpha.-[2-(4-trifluoromethoxyphenylthio)-5-furyl]-N-cyclopentylnitrone.
CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a divisional, of application Ser. No. 09/245,130, filed Jan. 14, 1999 which claims the benefit of U.S. Provisional Application No. 60/071,626, filed Jan. 16, 1998, which application is incorporated herein by reference in its entirety.
US Referenced Citations (3)
Number |
Name |
Date |
Kind |
4128658 |
Price et al. |
Dec 1978 |
|
5591761 |
Chan et al. |
Jan 1997 |
|
5942507 |
Kelleher et al. |
Aug 1999 |
|
Divisions (1)
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Number |
Date |
Country |
Parent |
245130 |
Jan 1999 |
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