Claims for Patent: 5,804,593

Summary for Patent: 5,804,593

Title:	.alpha.-Amino sulfonyl hydroxamic acids as matrix metalloproteinase inhibitors
Abstract:	A compound of formula I or pharmaceutical acceptable salts thereof, ##STR1## wherein R.sub.1 is isopropyl, 2-methylbut-2yl, phenyl, benzyl, or 1H-indol-3ylmethyl; R.sub.2 is n-octyl, phenyl, or phenyl substituted with methoxy, fluoro, or bromo, are matrix metalloproteinase inhibitors.
Inventor(s):	Warpehoski; Martha A. (Portage, MI), Mitchell; Mark Allen (Kalamazoo, MI), Jacobsen; Eric Jon (Portage, MI)
Assignee:	Pharmacia & Upjohn Company (Kalamazoo, MI)
Application Number:	08/953,940
Patent Claims:	1. A compound of formula I ##STR14## or pharmaceutical acceptable salts thereof wherein R.sub.1 is a) isopropyl, b) 2-methylbut-2yl c) phenyl, d) benzyl, or e) 1H-indol-3ylmethyl; and R.sub.2 is a) n-octyl, b) phenyl, or c) phenyl substituted with methoxy, fluoro, or bromo. 2. A compound of claim 1 wherein R.sub.2 is selected from the group consisting of n-octyl, phenyl, p-methoxyphenyl, p-fluorophenyl, or p-bromophenyl. 3. A compound of claim 1 which is a. N-Hydroxy-2(R)-[(4- methoxybenzenesulfonyl) amino]-3-(3-indolyl)-propanamide, b. N-Hydroxy-2(R)-[(benzenesulfonyl)amino]-3-(3-indolyl)-propanamide, c. N-Hydroxy-2(R)-[(4-fluorobenzenesulfonyl)amino]-3-(3-indolyl)-propanamide, d. N-Hydroxy-2(R)-[(4-methoxybenzenesulfonyl)amino]-3-phenyl-propanamide, e. N-Hydroxy-2(R)-[(4-bromobenzenesulfonyl)amino]-3-(3-indolyl)-propanamide, f. N-Hydroxy-2(R)-[(n-octylsulfonyl)amino]-3-(3-indolyl)-propanamide, g. N-Hydroxy-2(R)-[(4-methoxybenzenesulfonyl)amino]-2-phenyl acetamide, h. N-Hydroxy-2(R)-[(4-methoxybenzenesulfonyl)amino]-3-methyl butanamide, i. N-Hydroxy-2(R)-[(benzenesulfonyl)amino]-3-methyl butanamide, or j. N-Hydroxy-2(R)-[(4-methoxybenzenesulfonyl)amino]-3,3-dimethyl pentanamide. 4. A method of inhibiting excess matrix metalloproteinase which comprises administering to a patient in need thereof an effective amount of a compound of claim 1. 5. A method of claim 4 wherein the matrix metalloproteinase is stromelysin, collagenase, and gelatinase. 6. A method of treating a disease involving connective tissue degradation which comprises administering to a patient in need thereof an effective amount of a compound of claim 1. 7. A method of claim 6 wherein the disease related to connective tissue degradation is osteoarthrits, rheumatoid arthritis, septic arthritis, osteopenias, osteoporosis, tumor metastasis, periodontitis, gingivitis, corneal ulceration, dermal ulceration, or gastric ulceration. 8. The method of claim 4 wherein the effective amount of the compound of claim 1 is administered orally, parenterally, or topically in a pharmaceutical composition. 9. The method of claim 6 wherein the effective amount of the compound of claim 1 is administered orally, parenterally, or topically in a pharmaceutical composition. 10. The method of claim 4 or 6 wherein said compound is administered in an amount of from about 0.1 to about 100 mg/kg of body weight/day. 11. A pharmaceutical composition which comprises an amount of the compound of claim 1 effective to inhibit excess matrix metalloproteinase and a pharmaceutically acceptable carrier.

Details for Patent 5,804,593

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Smith & Nephew, Inc.	SANTYL	collagenase	Ointment	101995	06/04/1965		2039-03-29