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cataract/protease

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Substituted amino bicyclic-.beta.-lactam penam and cepham derivatives as cysteine protease inhibitors

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BACKGROUND OF INVENTION Cysteine proteases, such as cathepsins B, H, K, L, S, and O.sub.2, containing a highly reactive cysteine residue with a free thiol group at the active site have been known as playing an important role in certain conditions distinguished by aberrant protein turnover such as:

Sulfonamide derivatives

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BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel sulfonamide derivative. More particularly, it relates to a novel sulfonamide derivative or a salt thereof which shows a strong inhibitory activity against cysteine protease such as calpain, cathepsin B,

Aminoketone derivatives

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FIELD OF THE INVENTION This invention relates to novel aminoketone derivatives and, in particular, to novel aminoketone derivatives and their pharmaceutically acceptable salts which strongly inhibit thiol protease such as papain, cathepsin B, cathepsin H, cathepsin L and calpain or the

.alpha.-aminoketone derivatives

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FIELD OF THE INVENTION This invention relates to novel .alpha.-aminoketone derivatives and, in particular, to novel .alpha.-aminoketone derivatives and their pharmaceutically acceptable salts which strongly inhibit thiol protease such as papain, cathepsin B, cathepsin H, cathepsin L and calpain or
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