Inhibitors of cathepsin S

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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Details

C514S410000, C514S367000, C548S233000, C548S219000, C548S235000, C548S455000, C548S159000, C548S218000

Reexamination Certificate

active

10868459

ABSTRACT:
The present invention provides compounds, compositions and methods for the selective inhibition of cathepsin S. In a preferred aspect, cathepsin S is selectively inhibited in the presence of at least one other cathepsin isozyme. The present invention also provides methods for treating a disease state in a subject by selectively inhibiting cathepsin S.

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R. L. Thurmond et al., Jan. 2004, The Journal of Pharmacology and Experimental Therapeutics, vol. 308, No. 1, p. 268-276.
Bania, J. et al.: “Human cathepsin S, but not cathepsin L, degrades efficiently MHC class II-associated invariant chain in nonprofessional APCs” PNAS; vol. 100, No. 11; pp. 6664-6669 (May 27, 2003).

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