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Basic medicinal chemistry based on behavioral structure-building regulation of protein

Research Project

Project/Area Number 24790119
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Drug development chemistry
Research InstitutionTokyo University of Pharmacy and Life Science

Principal Investigator

AOYAMA hiroshi  東京薬科大学, 薬学部, 准教授 (40374699)

Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2012: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywords虚血/再灌流障害 / HCV / フォールディング / ダントロレン / 虚血・再灌流障害 / ミトコンドリア / C型肝炎 / 虚血性疾患 / PTP
Research Abstract

In this study, we tried to establish innovative drug development methodology by using a basic medicinal chemistry based on behavioral structure-building regulation of protein. A target of this study is folding regulatory factor, and illness to intend for both ischemia/reperfusion induced cell death and hepatitis C virus reproduction. As a result, we succeeded in development of compounds which have inhibitory effect of Ca2+-induced mitochondrial swelling. These compounds were considered to be capable of inhibitor for the ischemia/reperfusion induced cell death.

Report

(3 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • Research Products

    (2 results)

All 2013 2012

All Journal Article (2 results) (of which Peer Reviewed: 2 results)

  • [Journal Article] Novel Strategy for Synthesis of Substituted Benzimidazo[1,2-a]quinolines2013

    • Author(s)
      Jun-ya Kato, Yutaro Ito, Ryosuke Ijuin, Hiroshi Aoyama, Tsutomu Yokomatsu
    • Journal Title

      Organic Letters

      Volume: 15 Issue: 14 Pages: 3794-3797

    • DOI

      10.1021/ol4017723

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Small-molecular inhibitors of Ca2+-induced mitochondrial permeability transition (MPT) derived from muscle relaxant dantrolene.2012

    • Author(s)
      Shinpei Murasawa
    • Journal Title

      Bioorganic & Medicinal Chemistry

      Volume: 20 Issue: 21 Pages: 6384-6393

    • DOI

      10.1016/j.bmc.2012.08.062

    • Related Report
      2013 Final Research Report 2012 Research-status Report
    • Peer Reviewed

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Published: 2013-05-31   Modified: 2019-07-29  

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