摘要 |
The present invention relates to interleukin-1beta converting enzyme inhibitors having the formula: R is a carbocyclic or heterocyclic ring; R<SUP>1 </SUP>is a cysteine trap; R<SUP>2a</SUP>, R<SUP>2a'</SUP>, R<SUP>2b</SUP>, and R<SUP>2b'</SUP> are each independently hydrogen, C<SUB>1</SUB>-C<SUB>4 </SUB>alkyl, C<SUB>1</SUB>-C<SUB>4 </SUB>alkoxy, and mixtures thereof; or R<SUP>2a'</SUP> and R<SUP>2b'</SUP> can taken together to form a double bond; L and L<SUP>1 </SUP>are linking groups having the formula: T is selected from the group consisting of: i) -NR<SUP>6</SUP>-; ii) -O-; iii) -NR<SUP>6</SUP>S(O)<SUB>2</SUB>-; iv) -S(O)<SUB>2</SUB>NR<SUP>6</SUP>-; and v) mixtures thereof; R<SUP>6 </SUP>is hydrogen, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>20 </SUB>linear, branched, or cyclic alkyl, C<SUB>6</SUB>-C<SUB>20 </SUB>aryl, C<SUB>7</SUB>-C<SUB>20 </SUB>alkylenearyl, and mixtures thereof; the indices w, w<SUP>1</SUP>, and w<SUP>2 </SUP>are each independently 0 or 1; i) hydrogen; ii) C<SUB>1</SUB>-C<SUB>4 </SUB>linear, branched, and cyclic alkyl; iii) R<SUP>3a </SUP>and R<SUP>3b </SUP>or R<SUP>4a</SUP>, and R<SUP>4b </SUP>can be taken together to form a carbonyl unit; iv) two R<SUP>3a </SUP>or two R<SUP>3b </SUP>units from adjacent carbon atoms or two R<SUP>4a </SUP>or two R<SUP>4b </SUP>units from adjacent carbon atoms can be taken together to form a double bond; and v) mixtures thereof; the index m is from 0 to 5; the index n is from 0 to 5.
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