Abstract
A new series of 5-glycylamino-2-substituted-phenyl-1,3-dioxacycloalkanes were designed and synthesized. The anti-inflammatory activities of these compounds were tested using the xylene-induced mouse ear edema model. Sixteen of these new compounds exhibited comparable or better anti-inflammatory activities than aspirin suggesting that they can be further developed as potential anti-inflammatory drug leads. In addition, treatment with these anti-inflammatory agents did not prolong tail bleeding time in mice. The structure/activity relationships were also analyzed among these compounds. Considering their good efficacy and safety profiles, some 5-glycylamino-2-substituted-phenyl-1,3-dioxacycloalkanes are worthy to be explored further in assessing the possible link between anti-inflammation and cancer prevention.
| Original language | English |
|---|---|
| Pages (from-to) | 1764-1774 |
| Number of pages | 11 |
| Journal | Bioorganic and Medicinal Chemistry |
| Volume | 16 |
| Issue number | 4 |
| DOIs | |
| State | Published - Feb 15 2008 |
Keywords
- 5-Glycylamino-2-substituted-phenyl-1,3-dioxacycloalkanes
- Anti-inflammatory activity
- Chemoprevention
- Structure-activity relationship
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