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Research on IDO inhibitor as anticancer agent

Research Project

Project/Area Number 25460149
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Drug development chemistry
Research InstitutionKogakuin University (2015)
Okayama University (2013-2014)

Principal Investigator

MATSUNO KENJI  工学院大学, 先進工学部, 教授 (50433214)

Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywordsリード化合物 / 抗がん剤 / がん免疫療法剤 / IDO / 免疫寛容 / 構造活性相関 / 創薬 / 阻害剤 / in vivo活性 / 活性増強 / 新規ケモタイプ / 評価系構築
Outline of Final Research Achievements

The design, synthesis and biological evaluations for our original IDO inhibitors were conducted. We succeeded enhancement of IDO enzyme inhibition, as well as cellular IDO inhibition. As the result of our efforts, many potent analogues were identified. Furthermore, all potent IDO inhibitors demonstrated in vivo efficacy. The activity would be attributed to IDO inhibition since inactive IDO inhibitor did NOT show the in vivo activity.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (5 results)

All 2016 2015 Other

All Presentation (4 results) (of which Int'l Joint Research: 2 results) Remarks (1 results)

  • [Presentation] BENZIMIDAZOLE ANALOGUES AS KYNURENINE PRODUCTION INHIBITOR WITHOUT INDOLEAMINE 2,3-DIOXYGENASE INHIBITION2016

    • Author(s)
      Fukuda, M.; Suzuki, K.; Sasaki, T.; Miyachi, H.; Waki, M.; Asai, A.; Hashimoto, T.; Ohno, O.; Takikawa, O.; Matsuno, K.
    • Organizer
      XXIV EFMC International Symposium on Medicinal Chemistry
    • Place of Presentation
      Manchester, UK
    • Year and Date
      2016-08-28
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Cyclisation of Benzylisothiourea Provided Kynurenine Production Inhibitor without Indoleamine 2,3-Dioxygenase Inhibition.2015

    • Author(s)
      Fukuda, M.; Miyachi, H.; Waki, M.; Asai, A.; Takikawa, O.; Matsuno, K.
    • Organizer
      EFMC-ASMC'15 6th EFMC International Symposium on Advances in Synthetic and Medicinal Chemistry
    • Place of Presentation
      Rehovot, Israel
    • Year and Date
      2015-11-15
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Indoleamine 2,3-dioxygenase (IDO) 阻害活性を有するbenzimidazole系化合物の創製

    • Author(s)
      福田美和、脇稔、浅井章良、滝川修、宮地弘幸、松野研司
    • Organizer
      日本薬学会第134年会
    • Place of Presentation
      熊本市
    • Related Report
      2013 Research-status Report
  • [Presentation] Benzimidazole 構造を有する新規indoleamine 2,3-dioxygenase (IDO) 阻害剤の合成と

    • Author(s)
      福田美和、脇稔、浅井章良、滝川修、宮地弘幸、松野研司
    • Organizer
      第31回メディシナルケミストリーシンポジウム
    • Place of Presentation
      広島市
    • Related Report
      2013 Research-status Report
  • [Remarks] キヌレニン産生経路を標的とした医薬化学研究

    • URL

      http://www.ns.kogakuin.ac.jp/~wwa1068/research_Kynurenine.html

    • Related Report
      2015 Annual Research Report

URL: 

Published: 2014-07-25   Modified: 2019-07-29  

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