Abstract
A new class of 2,5-disubstituted-dioxacycloalkanes were designed and synthesized via stereoselective synthetic method as cancer chemoprevention agents. The anti-inflammatory activities of these compounds were tested using the xylene-induced mouse ear edema model. Some of these compounds exhibited comparable or better anti-inflammatory activities than that of aspirin suggesting that they can be further developed as potential anti-inflammatory drug lead compounds. In addition, treatment of these anti-inflammatory agents did not prolong tail bleeding time in mice. The structure/activity relationships were also analyzed among these compounds.
| Original language | English |
|---|---|
| Pages (from-to) | 4775-4799 |
| Number of pages | 25 |
| Journal | Bioorganic and Medicinal Chemistry |
| Volume | 15 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 15 2007 |
Keywords
- 2,5-Disubstituted-dioxacycloalkanes
- Anti-inflammatory activity
- Chemoprevention agents
- Stereoselective synthesis
- Structure-activity relationship study
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