Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376720 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
Abstract
Novel diazirine or biotin-labeled tanshinone probes were synthesized and evaluated for TRAP inhibitory activity against RANKL-induced osteoclastogenesis in RAW264.7 cells. We found that diazirine-labeled derivatives (18 and 20) are potent inhibitors of RANKL-induced osteoclastogenesis. IC50 values were 18.02 and 15.00 μM, respectively. These probes will be useful reagents for investigating tanshinone–proteins interactions.
Graphical abstractNovel diazirine or biotin-labeled tanshinone probes were synthesized and evaluated for TRAP inhibitory activity against RANKL-induced osteoclastogenesis in RAW264.7 cells.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jin-Soo Lee, Sun-Young Han, Myong Sang Kim, Chan-Mo Yu, Myung Hee Kim, Seong Hwan Kim, Yong Ki Min, Bum Tae Kim,