Abstract
The design, synthesis, and biological evaluation of structurally novel N-cyanopyrazolidine and N-cyanohexahydropyridazine derivatives as cathepsin inhibitors are described. In vitro assay reveals that several compounds exhibit highly potent and selective profiles against cathepsins K or S.
Original language | English |
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Pages (from-to) | 1467-1471 |
Number of pages | 5 |
Journal | Bulletin of the Korean Chemical Society |
Volume | 29 |
Issue number | 8 |
DOIs | |
Publication status | Published - 2008 Aug 20 |
All Science Journal Classification (ASJC) codes
- Chemistry(all)