Abstract
The synthesis and structure-activity relationships of a novel series of substituted quercetins that activates peroxisome proliferator-activated receptor gamma (PPARγ) are reported. The PPARγ agonistic activity of the most potent compound in this series is comparable to that of the thiazolidinedione-based antidiabetic drugs currently in clinical use.
| Original language | English |
|---|---|
| Pages (from-to) | 142-150 |
| Number of pages | 9 |
| Journal | Archives of Pharmacal Research |
| Volume | 28 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 28 Feb 2005 |
Bibliographical note
Funding Information:This study was financially supported by Chonnam National University in the program, 2001.
Keywords
- Antidiabetic agents
- Malonate
- Quercetin
- Thiazolidinedione
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