N-substituted-heteroaryloxy-aryl-spiro-pyrimidine-2,4,6-trio...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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Details

C514S231500, C514S241000, C514S269000, C544S180000, C544S231000, C544S006000, C544S070000, C544S403000, C540S492000, C540S485000, C540S543000

Reexamination Certificate

active

06900201

ABSTRACT:
The present invention relates to N-substituted-heteroaryloxy-aryl-spiro-pyrimidine-2,4,6-trione metalloproteinase inhibitors of the formulawherein ring X is a 5-7 membered heterocyclic ring, and wherein A, Y, B, and G are as defined in the specification; and to pharmaceutical compositions and methods of treating inflammation, cancer and other disorders.

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Mitchell, P.G., et al., “Cloning, Expression, and Type II Collagenolytic Activity of Matrix Metalloproteinase-13 from Human Osteoarthritic Cartilage,”J. Clin. Invest., 97, 761-768 (1996).
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Lednicer, D., et al.,The Organic Chemistry of Drug Synthesis, 1, 167-277.
Cawston, T.E., et al., “A Rapid and Reproducible Assay for Collagenase Using [1-14C] Acetylated Collagen,”Anal. Biochem.99(2), 340-345 (1979).
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