Acyl dipeptides as reversible caspase inhibitors. Part 2: further optimization

Bioorganic & Medicinal Chemistry Letters(2003)

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摘要
A new structural class of broad spectrum caspase inhibitors was optimized for its activity against caspases 1, 3, 6, 7, and 8. The most potent compound had low nanomolar broad spectrum activity, in particular, single digit nanomolar inhibitory activity against caspase 8.
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