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Development of silicon-containing units as expanded bioisosters

Research Project

Project/Area Number 16K15137
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Drug development chemistry
Research InstitutionThe University of Tokyo

Principal Investigator

HASHIMOTO Yuichi  東京大学, 定量生命科学研究所, 教授 (90164798)

Co-Investigator(Renkei-kenkyūsha) FUJII shinya  
Research Collaborator FUJII shinya  
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Keywordsケイ素 / バイオアイソスター / 核内受容体 / 構造展開 / 構造変換 / プレグナンX受容体 / チュブリン / シラノール / エストロゲン受容体 / 酸性度 / アンドロゲン受容体 / グルココルチコイド受容体
Outline of Final Research Achievements

Application of silyl functionalities is one of promising strategies for development of novel and distinctive biologically active compounds. Exchange of carbon atom of various biologically active compounds to silicon atom, that is called sila-substitution, have been intensively investigated, and the results suggest that sila-substitution is effective for alteration of activity profiles. In addition to the simple C/Si exchange, by focusing on the intrinsic characteristics of silicon being different from those of carbon, several novel approaches for utilizing silicon atom in medicinal chemistry have been proposed. Thus, the results indicate that the usage of silicon-containing unit increases possible options of structural development and has great potential for enlarging the chemical space of medicinal chemistry.

Academic Significance and Societal Importance of the Research Achievements

新規な汎用性のあるバイオアイソスターの開発は医薬化学の重点課題の一つである。本研究において、(1)光や熱に不安定なシスオレフィンを安定なケイ素に代替できることを示し、また、(2)ケイ素の特性(電気陰性度/脂溶性/結合長/分極性/分子間力など)によって、活性変換(アゴニスト・アンタゴニスト)や標的選択性の変換、新たな活性の付与、等が可能であることを示した。本研究成果により、生物活性物質・医薬シーズの分子設計戦略に多様性を付与し、そのケミカルスペースの拡大に貢献することができたと考える。

Report

(4 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (15 results)

All 2018 2017 2016

All Journal Article (5 results) (of which Peer Reviewed: 5 results,  Acknowledgement Compliant: 3 results) Presentation (10 results) (of which Int'l Joint Research: 2 results,  Invited: 1 results)

  • [Journal Article] Development of novel silanol-based human pregnane X receptor (PXR) agonists with improved receptor selectivity.2018

    • Author(s)
      Toyama H, Shirakawa H, Komai M, Hashimoto Y, Fujii S.
    • Journal Title

      Bioorg. Med. Chem.

      Volume: 26 Issue: 15 Pages: 4493-4501

    • DOI

      10.1016/j.bmc.2018.07.038

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Progress in the medicinal chemistry of silicon. -C/Si-Exchange and beyond-2017

    • Author(s)
      Fujii, S.,* Hashimoto, Y.
    • Journal Title

      Future Med. Chem.

      Volume: in press Issue: 5 Pages: 485-505

    • DOI

      10.4155/fmc-2016-0193

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Journal Article] Discovery of N-(1-(3-(4-phenoxyphenyl)-1,2,4-oxadiazol-5-yl)ethyl)acetamides as novel acetyl-CoA carboxylase 2 (ACC2) inhibitors with peroxisome proliferator-activated receptor α/δ (PPARα/δ) dual agonistic activit2016

    • Author(s)
      Shogo Okazaki, Tomomi Noguchi-Yachide, Taki Sakai, Minoru Ishikawa, Makoto Makishima, Yuichi Hashimoto, Takao Yamaguchi
    • Journal Title

      Bioorganic & Medicinal Chemistry

      Volume: 24 Issue: 21 Pages: 5258-5269

    • DOI

      10.1016/j.bmc.2016.08.045

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] Efficient protein knockdown of HaloTag-fused proteins using hybrid molecules consisting of IAP antagonist and HaloTag ligand2016

    • Author(s)
      Shusuke Tomoshige, Yuichi Hashimoto, Minoru Ishikawa
    • Journal Title

      Bioorganic & Medicinal Chemistry

      Volume: 24 Issue: 14 Pages: 3144-3148

    • DOI

      10.1016/j.bmc.2016.05.035

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] Altered activity profile of a tertiary silanol analog of multi-targeting nuclear receptor modulator T0901317.2016

    • Author(s)
      Hirozumi Toyama, Shoko Sato, Hitoshi Shirakawa, Michio Komai, Yuichi Hashimoto, Shinya Fujii
    • Journal Title

      Bioorganic and Medicinal Chemistry Letters

      Volume: 26 Pages: 1817-1820

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] ビスフェノール構造を基盤としたケイ素官能基の構造物性および構造活性相関2018

    • Author(s)
      松本雄一朗、橋本祐一、藤井晋也
    • Organizer
      日本薬学会第138年会
    • Related Report
      2018 Annual Research Report
  • [Presentation] Silyl groups as fancy isosteres of cis-diatomic functionalities: Development of novel nuclear receptor modulators bearing silyl functionality2018

    • Author(s)
      Shinya Fujii, Hirosumi Toyama, Daisuke Kajita, Yuichi Hashimoto
    • Organizer
      RICT 2018 54th International Conference on Medicinal Chemistry
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 創薬化学における高周期元素の利用法の検討 - 種々の元素をリンカー構造に有するビスフェノール誘導体の構造物性相関および構造活性相関2018

    • Author(s)
      松本雄一朗、橋本祐一、藤井晋也
    • Organizer
      日本レチノイド研究会第29会学術集会
    • Related Report
      2018 Annual Research Report
  • [Presentation] ケイ素官能基をリンカー構造とするビスフェノール誘導体の構造物性相関と選択的エストロゲン受容体モジュレータへの展開2018

    • Author(s)
      松本雄一朗、橋本祐一、藤井晋也
    • Organizer
      第36回メディシナルケミストリーシンポジウム
    • Related Report
      2018 Annual Research Report
  • [Presentation] パーフルオロアルコール基の代替官能基としてのシラノール基の医薬的有用性の検討2017

    • Author(s)
      外山大純、橋本祐一、藤井晋也
    • Organizer
      日本ケミカルバイオロジー学会第12会年会
    • Related Report
      2017 Research-status Report
  • [Presentation] 新規骨格構造を有する非ステロイド型GRリガンドの探索と構造展開.2016

    • Author(s)
      吉岡広大、西山郵子、山田歩、影近弘之、橋本祐一、藤井晋也
    • Organizer
      日本レチノイド研究会第27回学術集会
    • Place of Presentation
      昭和薬科大学(東京都町田市)
    • Year and Date
      2016-10-22
    • Related Report
      2016 Research-status Report
  • [Presentation] 新規アンドロゲン受容体AF-1モジュレーターの構造活性相関.2016

    • Author(s)
      沼館慧剛、梅田香織、槇島誠、橋本祐一、藤井晋也
    • Organizer
      日本レチノイド研究会第27回学術集会
    • Place of Presentation
      昭和薬科大学(東京都町田市)
    • Year and Date
      2016-10-22
    • Related Report
      2016 Research-status Report
  • [Presentation] Structural and functional development of retinoids/steroids.2016

    • Author(s)
      Yuichi Hashimoto
    • Organizer
      International Conference for the 70th Anniversary of Pharmaceutical Society of Korea
    • Place of Presentation
      The-K Hotel Seoul(韓国)
    • Year and Date
      2016-10-18
    • Related Report
      2016 Research-status Report
    • Int'l Joint Research / Invited
  • [Presentation] アンドロゲン受容体AF-1モジュレーターの構造展開.2016

    • Author(s)
      沼館慧剛、谷内出友美、梅田香織、槇島誠、橋本祐一、藤井晋也
    • Organizer
      日本ケミカルバイオロジー学会第11回年会
    • Place of Presentation
      京都テルサ(京都府京都市)
    • Year and Date
      2016-06-15
    • Related Report
      2016 Research-status Report
  • [Presentation] PPARα/δデュアル転写誘導活性を有する新規ACC2阻害剤の創出.2016

    • Author(s)
      吉岡広大、西山郵子、山田歩、影近弘之、橋本祐一、藤井晋也
    • Organizer
      日本ケミカルバイオロジー学会第11回年会
    • Place of Presentation
      京都テルサ(京都府京都市)
    • Year and Date
      2016-06-15
    • Related Report
      2016 Research-status Report

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Published: 2016-04-21   Modified: 2020-03-30  

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