Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2005-03-22
2005-03-22
Ramsuer, Robert W. (Department: 1626)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Heterocyclic carbon compounds containing a hetero ring...
C544S159000
Reexamination Certificate
active
06869951
ABSTRACT:
The present invention provides a matrix metalloproteinase inhibiting compound having structure (VIII) or a salt, an enantiomer, a diastereomer, a racemate, or a tautomer thereof. In other embodiments, the present invention provides a method of changing the conformation of a matrix metalloproteinase, a method of inhibiting a matrix metal metalloproteinase, and a method of treating osteoarthritis.
REFERENCES:
patent: 4595700 (1986-06-01), Donald et al.
patent: 6362183 (2002-03-01), Freskos et al.
patent: 6451791 (2002-09-01), Heintz et al.
patent: 0 757 037 (1997-02-01), None
patent: 0 757 984 (1997-02-01), None
patent: 0 780 386 (1997-06-01), None
patent: 0 950 656 (1999-10-01), None
patent: 11-236369 (1999-08-01), None
patent: 11-246527 (1999-09-01), None
patent: WO 9005719 (1990-05-01), None
patent: WO 9320047 (1993-10-01), None
patent: WO 9402466 (1994-02-01), None
patent: WO 9424140 (1994-10-01), None
patent: WO 9509841 (1995-04-01), None
patent: WO 9513289 (1995-05-01), None
patent: WO 9529892 (1995-11-01), None
patent: WO 9606074 (1996-02-01), None
patent: WO 9720824 (1997-06-01), None
patent: WO 9724117 (1997-07-01), None
patent: WO 9803166 (1998-01-01), None
patent: WO 9839315 (1998-09-01), None
patent: WO 9839329 (1998-09-01), None
patent: WO 9942433 (1999-08-01), None
Reinemer et al.,Structural Implifications for the role of the N terminus in the ‘superactivation’ of collagenases, FEBS Letters, 338:227-233 (1994).
Brünger,Free R value: a novel statistical quantity for assessing the accuracy of crystal structures, Nature, 355:472-475 (1992).
Denis et al.,Matrix metalloproteinase Inhibitors: Present achievements and future prospects, Investig. New Drugs, 15:175-185 (1997).
Gearing et al.,Processing of tumour necrosis factor-α precursor by metalloproteinases, Nature, 370:555-557 (1994).
Grams et al.,X-ray structures of human neutrophil collagenase complexed with peptide hydroxamate and peptide thiol Inhibitors—Implications for substrate binding and rational drug design, Eur. J. Biochem., 228:830-841 (1995).
Jones et al.,Improved methods for building protein models in electron density maps and the location of errors in these models, Acta Cryst., A47:110-119 (1991).
Kiyama et al.,Homology modeling of gelatinase catalytic domains and docking simulations of novel sulfonamide inhibitors, J. Med. Chem., 42:1723-1738 (1999).
Lovejoy et al.,Crystal structures of MMP-1 and -13 reveal the structural basis for selectivity of collagenase inhibitors, Nat. Struc. Biol., 6(3):217-221 (1999).
McGeehan et al.,Regulation of tumour necrosis factor-α processing by a metalloproteinase inhibitor, Nature, 370:558-561 (1994).
Mitchell et al.,Cloning, expression, and type II collagenolytic activity of matrix metalloproteinase-13 from human osteoarthritic cartilage, J. Clin. Invest., 97(3):761-768 (1996).
Morgunova et al.,Structure of human pro-matrix metalloproteinase-2: Activation mechanism revealed, Science, 284:1667-1670 (1999).
Nicholls et al.,Protein folding and association: Insights from the Interfacial and thermodynamic properties of hydrocarbons, Proteins, 11(4) 281-296 (1991).
Otwinowski,Oscillation data reduction program, in Proceedings of CCP-4 Study Weekend: Data Collection and Processing, 56-62 (1993).
Parks et al., Matrix Metalloproteinases, 32-33 (1998).
Rasmussen et al.,Matrix metalloproteinase inhibition as a novel anticancer strategy: A review with special focus on batimastat and marimastat, Pharmacol. Ther., 75(1):69-75 (1997).
Reboul et al.,The new collagenase, collagnease-3, is expressed and synthesized by human chondrocytes but not by synoviocytes, J. Clin. Invest., 97(9):2011-2019 (1996).
Schwartz et al.,Synthetic inhibitors of bacterial and mammalian interstitial collagenases, Prog. in Med. Chem., 29:271-334 (1992).
Tamura et al.,Highly selective and orally active inhibitors of type IV collagenase(MMP-9 and MMP-2);N-sulfonylamino acid derivatives, J. Med. Chem., 41:640-649 (1998).
PCT/US00/16323 (WO 01/05389) International Search Report and Transmittal, 9 pgs.
DeCrescenzo Gary A.
Howard Susan C.
McDonald Joseph J.
Shieh Huey S.
Stallings William C.
Harness & Dickey & Pierce P.L.C.
Pharmacia Corporation
Ramsuer Robert W.
Saeed Kamal
LandOfFree
Method of changing conformation of a matrix metalloproteinase does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Method of changing conformation of a matrix metalloproteinase, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Method of changing conformation of a matrix metalloproteinase will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3420243