Abstract
Design, synthesis and insight into the structure-activity relationship (SAR) of 1,3-disubstituted indazoles as novel HIF-1 inhibitors are described. In particular, the substituted furan moiety on indazole skeleton as well as its substitution pattern turns out crucial for the high HIF-1 inhibition.
| Original language | English |
|---|---|
| Pages (from-to) | 6297-6300 |
| Number of pages | 4 |
| Journal | Bioorganic and Medicinal Chemistry Letters |
| Volume | 21 |
| Issue number | 21 |
| DOIs | |
| State | Published - 1 Nov 2011 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Anti-cancer agent
- HIF-1α
- Hypoxia
- SAR (structure-activity relationship)
- YC-1
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