2016 Fiscal Year Final Research Report
Search for target proteins utilizing the stable equivalents of resorvins, pro-resolving lipid mediators
Project/Area Number |
15K18898
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Drug development chemistry
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Research Institution | Hokkaido University |
Principal Investigator |
FUKUDA Hayato 北海道大学, 薬学研究院, 助教 (30434450)
|
Project Period (FY) |
2015-04-01 – 2017-03-31
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Keywords | レゾルビン / レゾルビンE2 / 安定等価体 / 標的タンパク質 / 炎症収束 / シクロプロパン / デオキシレゾルビン |
Outline of Final Research Achievements |
It was decided to synthesize deoxyresolvine E2 in order to confirm the importance of the hydroxyl group of resolvin E2, then 5-deoxyresolvin E2, 18-deoxyresolvin E2, and 5,18-dideoxyresolvin E2 were efficiently synthesized by exploiting the synthetic method of resolvin E2. These synthesized compounds were evaluated by an anti-inflammatory activity test, so it was found that they all had the biological activity equivalent to that of resolvin E2. Therefore, it was suggested that the linker could extend from C-5 or C-18 of resolvin E2.
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Free Research Field |
創薬化学
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