IL-8 receptor antagonists
This invention relates to novel compounds and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).
1. A compound selected from the group consisting of:
N-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}-N′-(3-fluoro-2-methylphenyl)urea;
N-[4-chloro-2-hydroxy-3-(3-piperidinylsulfonyl)-phenyl]-N′-(3-fluoro-2-methylphenyl)urea;
N-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}-N′-(2-chloro-3-pyridinyl)urea; and
N-(2-chloro-3-fluorophenyl)-N′-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinyl-sulfonyl]phenyl}urea;
or a pharmaceutically acceptable salt thereof.
2. A compound according to claim 1 wherein the pharmaceutically acceptable salt is a hydrochloride salt.
3. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier or diluent.
4. A method of treating asthma, chronic obstructive pulmonary disease or adult respiratory distress syndrome in a mammal in need thereof which method comprises administering to said mammal an effective amount of a compound according to claim 1 .
5. The method according to claim 4 wherein the mammal is a human afflicted with chronic obstructive pulmonary disease.
6. The method according to claim 4 wherein the mammal is a human.
7. The compound which is N-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}-N′-(3-fluoro-2-methylphenyl)urea, or a pharmaceutically acceptable salt thereof.
8. A pharmaceutical composition comprising N-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}-N′-(3-fluoro-2-methylphenyl)urea, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent.
9. The compound which is N-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}-N′-(3-fluoro-2-methylphenyl)urea.
10. A pharmaceutical composition comprising N-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}-N′-(3-fluoro-2-methylphenyl)urea and a pharmaceutically acceptable carrier or diluent.
11. The compound which is N-(2-chloro-3-fluorophenyl)-N′-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}urea, or a pharmaceutically acceptable salt thereof.
12. A pharmaceutical composition comprising N-(2-chloro-3-fluorophenyl)-N′-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}urea, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent.
13. The compound which is N-(2-chloro-3-fluorophenyl)-N′-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}urea.
14. A pharmaceutical composition comprising N-(2-chloro-3-fluorophenyl)-N′-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}urea and a pharmaceutically acceptable carrier or diluent.
15. The compound according to claim 1 wherein the pharmaceutically acceptable salt is selected from the group consisting of hydrochloride, hydrobromide, sulfate, phosphate, methane sulfonate, ethane sulfonate, acetate, malate, tartrate, citrate, lactate, oxalate, succinate, fumarate, maleate, benzoate, salicylate, phenylacetate, and mandelate.
16. The compound according to claim 7 wherein the pharmaceutically acceptable salt is selected from the group consisting of hydrochloride, hydrobromide, sulfate, phosphate, methane sulfonate, ethane sulfonate, acetate, malate, tartrate, citrate, lactate, oxalate, succinate, fumarate, maleate, benzoate, salicylate, phenylacetate, and mandelate.
17. The compound which is N-[4-chloro-2-hydroxy-3-(3-piperidinylsulfonyl)-phenyl]-N′-(3-fluoro-2-methylphenyl)urea, or a pharmaceutically acceptable salt thereof.
18. The compound according to claim 11 wherein the pharmaceutically acceptable salt is selected from the group consisting of hydrochloride, hydrobromide, sulfate, phosphate, methane sulfonate, ethane sulfonate, acetate, malate, tartrate, citrate, lactate, oxalate, succinate, fumarate, maleate, benzoate, salicylate, phenylacetate, and mandelate.
19. A pharmaceutical composition comprising a compound according to claim 1 , or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or diluent.
20. A method of treating asthma, chronic obstructive pulmonary disease or adult respiratory distress syndrome in a human in need thereof comprising administering to said human an effective amount of a compound according to claim 7 .
21. A method of treating asthma, chronic obstructive pulmonary disease or adult respiratory distress syndrome in a human in need thereof comprising administering to said human an effective amount of a compound according to claim 9 .
22. A method of treating psoriasis, atopic dermatitis, osteoarthritis, rheumatoid arthritis, inflammatory bowel disease, Crohn's disease, or ulcerative colitis in a human in need thereof, comprising administering to said human an effective amount of a compound according to claim 1 .
23. A pharmaceutical composition comprising N-{4-chloro-2-hydroxy-3-[(3S)-3-piperidinylsulfonyl]phenyl}-N′-(3-fluoro-2-methylphenyl)urea, or a pharmaceutically acceptable salt thereof, or N-[4-chloro-2-hydroxy-3-(3-piperidinylsulfonyl)-phenyl]-N′-(3-fluoro-2-methylphenyl)urea, or a pharmaceutically acceptable salt thereof, in admixture with a pharmaceutically acceptable carrier or diluent for administration by intravenous, intramuscular, subcutaneous, intravaginal, intraperitoneal, oral inhalation, or intranasal means.
24. The compound according to claim 17 wherein the pharmaceutically acceptable salt is selected from the group consisting of hydrochloride, hydrobromide, sulfate, phosphate, methane sulfonate, ethane sulfonate, acetate, malate, tartrate, citrate, lactate, oxalate, succinate, fumarate, maleate, benzoate, salicylate, phenylacetate, and mandelate.
25. The compound which is N-[4-chloro-2-hydroxy-3-(3-piperidinylsulfonyl)-phenyl]-N′-(3-fluoro-2-methylphenyl)urea.
26. A pharmaceutical composition comprising N-[4-chloro-2-hydroxy-3-(3-piperidinylsulfonyl)-phenyl]-N′-(3-fluoro-2-methylphenyl)urea, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent.
27. A pharmaceutical composition comprising N-[4-chloro-2-hydroxy-3-(3-piperidinylsulfonyl)-phenyl]-N′-(3-fluoro-2-methylphenyl)urea, and a pharmaceutically acceptable carrier or diluent.
28. A method of treating a disease selected from the group consisting of asthma, chronic obstructive pulmonary disease, adult respiratory distress syndrome, psoriasis, atopic dermatitis, osteoarthritis, rheumatoid arthritis, inflammatory bowel disease, Crohn's disease, and ulcerative colitis in a human in need thereof, comprising administering to said human an effective amount of a compound according to claim 17 .
29. The method according to claim 28 wherein the disease is chronic obstructive pulmonary disease.
30. A method of treating a disease selected from the group consisting of asthma, chronic obstructive pulmonary disease, adult respiratory distress syndrome, psoriasis, atopic dermatitis, osteoarthritis, rheumatoid arthritis, inflammatory bowel disease, Crohn's disease, and ulcerative colitis in a human in need thereof, comprising administering to said human an effective amount of a compound according to claim 25 .
31. The method according to claim 30 wherein the disease is chronic obstructive pulmonary disease.