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Development of histamine H_3 receptor selective ligands based on the versatile chiral cyclopropane units.

Research Project

Project/Area Number 15590096
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Drug development chemistry
Research InstitutionHOKKAIDO UNIVERSITY

Principal Investigator

SHUTO Satoshi  Hokkaido Univ., Grad.School of Pharm.Sci., Prof., 大学院・薬学研究科, 教授 (70241346)

Project Period (FY) 2003 – 2004
Project Status Completed (Fiscal Year 2004)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2004: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2003: ¥1,800,000 (Direct Cost: ¥1,800,000)
Keywordsagonist / antagonist / conformationally restricted analogue / cyclopropane / drug design / histamine / H_3 receptor / H_1 receptor / 配座制御 / 創薬 / 受容体サブタイプ
Research Abstract

Highly selective H_3 agonists and also antagonists would not only be very useful as tools for pharmacological studies but would also be important as leads for the development of new drugs. We designed a series of cyclopropane-based conformationally restricted analogues of histamine, which were effectively synthesized from chiral cyclopropane units previously developed by us. Among these conformationally restricted analogues, (1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclopropane having the cis-cyclopropane structure was identified as a highly H_3-selective agonist. On the basis of these findings, cyclopropane-based H_3 selective antagonists were designed. These were designed by introducing an aromatic ring into the structure of the H_3 selective agonists found, since introduction of aromatic rings into the proper site of an agonist sometimes convert it into the corresponding antagonist, which has been recognized as "umbrella effect". These compounds were also synthesized from above chiral cyclopropane units, and some very strong H_3 receptor antagonists with selectivity were found. Thus, we successfully developed H_3 selective agonists and antagonists based on theoretical design using the versatile chiral cyclopropane units.

Report

(3 results)
  • 2004 Annual Research Report   Final Research Report Summary
  • 2003 Annual Research Report
  • Research Products

    (28 results)

All 2004 Other

All Journal Article (20 results) Book (2 results) Publications (6 results)

  • [Journal Article] Conformational and inframolecular studies of the protonation of Adenophostin analogues lacking the Adenine moiety.2004

    • Author(s)
      H.Dozol, et al.
    • Journal Title

      Biochim.Biophys.Acta-General Subjects 1671

      Pages: 1-8

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] The first 1,4-chelation-controlled nucleophilic addition to aldehydes with high stereoselectivity. A systematic study of stereoselectivity in the addition reaction of carbon nucleophiles to cis-substituted cyclopropanecarbaldehydes.2004

    • Author(s)
      Y.Kazuta, et al.
    • Journal Title

      Tetrahedron 60

      Pages: 6689-6703

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Annual Research Report 2004 Final Research Report Summary
  • [Journal Article] Oligodeoxynucleotides having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl)thymidines form stable hairpins.2004

    • Author(s)
      Y.Yamamoto, et al.
    • Journal Title

      Biochemistry 43

      Pages: 8690-8699

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] An efficient synthesis of β-C-glycosides based on the conformational restriction strategy : Lewis acid-promoted silane reduction of the anomeric position with complete stereoselectivity2004

    • Author(s)
      M.Terauchi, et al.
    • Journal Title

      Org.Lett. 6

      Pages: 3751-3754

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Highly stereoselective Grignard addition to cis-substituted C-cyclopropylaldonitiones. The bisected s-trans transition state can be stabilized effectively by the Lewis acid-coordination.2004

    • Author(s)
      Y.Kazuta, et al.
    • Journal Title

      J.Org.Chem. 69

      Pages: 9143-9150

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Stable hairpins having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl)thymidines.2004

    • Author(s)
      S.Shuto, et al.
    • Journal Title

      Nucleic Acids Res.Supplement. 48

      Pages: 67-68

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Chemistry of cyclic ADP-ribose and its analogs.2004

    • Author(s)
      S.Shuto, et al.
    • Journal Title

      Curr.Med.Chem. 11

      Pages: 827-845

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Annual Research Report 2004 Final Research Report Summary
  • [Journal Article] Conformational and intramolecular studies of the protonation of Adenophostin analogues lacking the Adenine moiety.2004

    • Author(s)
      H.Dozol, et al.
    • Journal Title

      Biochim.Biophys.Acta-General Subjects 1671

      Pages: 1-8

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Oligodeoxynucleotides having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl) thymidines form stable hairpins.2004

    • Author(s)
      Y.Yamamoto, et al.
    • Journal Title

      Biochemistry 43

      Pages: 8690-8699

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Annual Research Report 2004 Final Research Report Summary
  • [Journal Article] An efficient synthesis of β-C-glycosides based on the conformational restriction strategy : Lewis acid-promoted silane reduction of the anomeric position with complete stereoselectivity.2004

    • Author(s)
      M.Terauchi, et al.
    • Journal Title

      Org.Lett. 6

      Pages: 3751-3754

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Annual Research Report 2004 Final Research Report Summary
  • [Journal Article] Highly stereoselective Grignard addition to cis-substituted C-cyclopropylaldonitrones. The bisected s-trans transition state can be stabilized effectively by the Lewis acid-coordination.2004

    • Author(s)
      Y.Kazuta, et al.
    • Journal Title

      J.Org.Chem. 69

      Pages: 9143-9150

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Annual Research Report 2004 Final Research Report Summary
  • [Journal Article] Stable hairpins having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl) thymidines.2004

    • Author(s)
      S.Shuto, et al.
    • Journal Title

      Nucleic Acids Res.Supplement. 48

      Pages: 67-68

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Conformational and inframolecular studies of the protonation of Adenophostin analogues lacking the Adenine moiety.2004

    • Author(s)
      H.Dozol, et al.
    • Journal Title

      Biochim.Biophys. Acta-General Subjects 1671

      Pages: 1-8

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Stable hairpins having a loop consisting of 3'-deoxy-4'-C-(2-hydroxyethyl) thymidines.2004

    • Author(s)
      S.Shuto, et al.
    • Journal Title

      Nucleic Acids Res. Supplement 48

      Pages: 67-68

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Synthesis of 5'-methylenearisteromycin and its 2-fluoro congener with potent antimalarial activity due to inhibition of the parasite S-sdenosylhomocysteine hydrolase.

    • Author(s)
      C.Takagi, et al.
    • Journal Title

      Org.Biomol.Chem. (in press)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Synthesis of 4,8-anhydro-D-glycero-D-ido-nonanitol 1,6,7-trisphosphate as a novel IP_3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy.

    • Author(s)
      M.Terauchi, et al.
    • Journal Title

      Tetrahedron (in press)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Synthesis of 5'-methylenearisteromycin and its 2-fluoro congener with potent antimalarial activity due to inhibition of the parasite S-sdenosylhomocysteine hydrolase.

    • Author(s)
      C.Takagi, et al.
    • Journal Title

      Org.Biomol.Chem. (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Synthesis of 4,8-anhydro-D-glycero-D-idononanitol-1,6,7-trisphosphate as a novel IP_3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy.

    • Author(s)
      M.Terauchi, et al.
    • Journal Title

      Tetrahedron (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Synthesis of 5'-methylenearisteromycin and its 2-fluoro congener with potent antimalarial activity due to inhibition of the parasite S-sdenosylhomocysteine hydrolase.

    • Author(s)
      C.Takagi, et al.
    • Journal Title

      Org.Biomol.Chem. (in press)

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Synthesis of 4,8-anhydro-D-glycero-D-ido-nonanitol 1,6,7-trisphosphate as a novel IP_3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy.

    • Author(s)
      M.Terauchi, et al.
    • Journal Title

      Tetrahedron (in press)

    • Related Report
      2004 Annual Research Report
  • [Book] オングストロムの分子設計 ナノバイオエンジニアリング,化学フロンティア(杉本直己編)2004

    • Author(s)
      周東 智
    • Total Pages
      13
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Book] オングストロムの分子設計 ナノバイオエンジニアリング,化学フロンティア(杉本直己 編)2004

    • Author(s)
      周東 智
    • Total Pages
      13
    • Related Report
      2004 Annual Research Report
  • [Publications] Y.Kazuta, et al.: "1S,2S)-2-(2-Aminoethyl)-1-(1H-imidazol-4-yl)cyclopropane, a highly selective agonist for the histamine H_3 receptor, having a cis-cyclopropane structure"J.Med.Chem.. 42. 1980-1988 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Y.Kazuta, et al.: "A systematic study of the hydride reduction of cyclopropyl ketones with structurally simplified substrates"J.Org.Chem.. 68. 3511-3521 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] M.Sukeda, et al.: "The first radical method for the introduction of an ethynyl group using a silicon tether and its application to the synthesis of 2'-deoxy-2'-C-ethynylnucleosides"J.Org.Chem.. 68. 3465-3475 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] A.Tamura, et al.: "Control of the α/β-stereoselectivity in Lewis acid-promoted C-glycosidation using a controlling anomeric effect based on the conformational restriction strategy"Angew.Chem.Int.Ed.. 42. 1021-1023 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] S.Shuto, et al.: "Convergent Synthesis and Unexpected Ca^<2+>-Mobilizing Activity of 8-Substituted Analogues of Cyclic ADP-Carbocyclic-Ribose"J.Med.Chem.. 42. 4741-4749 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Y.Ohmori, et al.: "A method for designing conformationally restricted analogues based on allylic strain"J.Med.Chem.. 42. 5326-5333 (2003)

    • Related Report
      2003 Annual Research Report

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Published: 2003-04-01   Modified: 2016-04-21  

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