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2013 Fiscal Year Final Research Report

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

Research Project

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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
Keywords虚血/再灌流障害 / HCV / フォールディング / ダントロレン
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.

  • Research Products

    (1 results)

All 2012

All Journal Article (1 results) (of which Peer Reviewed: 1 results)

  • [Journal Article] Small- molecular Inhibitors of Ca^2+-induced Mitochondrial Permeability Transition (MPT) Derived from Muscle Relaxant Dantrolene, Bioorg2012

    • Author(s)
      Shinpei Murasawa, Katsuya Iuchi, Shinichi Sato, Tomomi Noguchi-Yachide, Mikiko Sodeoka, Tsutomu Yokomatsu, Kosuke Dodo, Yuichi Hashimoto, and Hiroshi Aoyama
    • Journal Title

      Med. Chem

      Volume: 20 Pages: 6384-6393

    • DOI

      10.1016/j.bmc.2012.08.062

    • Peer Reviewed

URL: 

Published: 2015-06-25  

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