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2016 Fiscal Year Final Research Report

Search for target proteins utilizing the stable equivalents of resorvins, pro-resolving lipid mediators

Research Project

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Project/Area Number 15K18898
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Drug development chemistry
Research InstitutionHokkaido 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
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.

Free Research Field

創薬化学

URL: 

Published: 2018-03-22  

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