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Studies on the stereochemistry of new macrolides from marine organisms for research and development of drug molecules

Research Project

Project/Area Number 07558208
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section展開研究
Research Field Bioorganic chemistry
Research InstitutionCHIBA UNIVERSITY (1997)
Hokkaido University (1995-1996)

Principal Investigator

ISHIBASHI Masami  Chiba University, Faculty of Pharmaceutical Sciences, Professor, 薬学部, 教授 (90212927)

Project Period (FY) 1995 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 1997: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1996: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsMarine natural products / Macrolide / Sponge / Dinoflagellate / Stereochemistry / Chiral carbon / Synthesis / Structure elucidation / 過鞭毛藻
Research Abstract

In this research project, we investigated on determination of absolute stereochemistry of many chiral centers contained in bioactive marine natural products classified as macrolides, which were isolated from marine sponges and dinoflagellates by our research group.
1.Theonezolide A is a novel cytotoxic 37-membered macrolide isolated from the Okinawan marine sponge Theonella sp., having unique bioactivity of induction of rabbit platelet shape change and aggregation. Theonezolide A contains 23 chiral centers, among which the absolute configuration of one chiral center at the terminal position (C-75) was determined as R on the basis of synthesis of a degradation product. As to the C-4-C-17 fragment, which was obtained by ozonolysis of the macrolide, the relative configurations of two 1,3-diol type moieties were suggested as both syn from the synthesis of model compounds. Four structures therefore remained to be likely, and two possible diastereomers were synthesized as optically active forms. Comparison of their spectral and optical data established the absolute configuration of four chiral centers contained in the C-4-C-17 fragment as 8S,10R,14S,16S.
2.Amphidinolides are unique macrolides obtained from cultured marine dinoflagellate Amphidinium sp. A diastereomer of the C-1-C-9 fragment of amphidinolide C,one of the potent cytotoxic macrolides isolated from this dinoflagellate, was synthesized to provide an authentic sample for the degradation studies. To provide an adequate quantity of the natural product to supply for degradation experiments, further large-scale culturing of the dinoflagellate Amphidinium sp.was continued. During further examinations on the extracts of the cultured cells of this dinoflagellate, two new macrolides, amphidinolides R and S,were isolated and their structures including absolute configuration were elucidated on the basis of spectroscopic data as well as chemical experiments.

Report

(4 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report
  • 1995 Annual Research Report
  • Research Products

    (18 results)

All Other

All Publications (18 results)

  • [Publications] M.Ishibashi: "Studies on the Marolides from Marine Dinoflagellate Amphidinium sp.:Structures of Amphidinolides R and S and a Succinate Feeding Experiment" Tetrahedron. 53. 7827-7832 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] M.Ishibashi: "Amphidinolides:Unique Macrolides from Marine Dinoflagellates" Heterocycles. 44. 543-572 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] J.Kobayashi: "Studies on the Stereochemistry of Theonezolides A〜C:Elucidation of the Relative Configurations of 1,3-Diol Moietiesof the C-4〜C-17Fragment" Heterocycles. 47(印刷中). (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] M.Sato: "Studies on the Stereochemistry of Theonezolides A〜C:Determination of the Absolute Stereochemistry of the C-4〜C-17 Fragment" Tetrahedron. 54(印刷中). (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] M.Ishibashi: "Amphidinolides O and P,Novel 15-Membered Macrolides from the Dinoflagellate Amphidinium sp. : Analysis of the Relative Stereochemistry and Stable Solution Conformation" Journal of Organic Chemistry. 60. 6062-6066 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] J.Kobayashi: "Amphidinolide Q,a Novel 12-Membered Macrolide from the Cultured Marine Dinoflagellate Amphidinium sp." Tetrahedron Letters. 37. 1449-1450 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] H.Ishiyama: "Studies on the Stereochemistry of Amphidinolides : Synthesis of a Diastereomer of the C-1-C-9 Fragment of Amphidinolide C" Chemical and Pharmaceutical Bulletin. 44. 1819-1822 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] M.Ishibashi: "Studies on the Macrolides from Marine Dinoflagellate Amphidinium sp. : Structures of Amphidinolides R and S and a Succinate Feeding Experiment" Tetrahedron. 53. 7827-7832 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] M.Ishibashi: "Amphidinolides : Unique Macrolides from Marine Dinoflagellates" Heterocycles. 44. 543-572 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] J.Kobayashi: "Studies on the Stereochemistry of Theonezolides A-C : Elucidation of the Relative Configurations of 1,3-Diol Moieties of the C-4-C-17 Fragment" Heterocycles. 47 (in pres). (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] M.Sato: "Studies on the Stereochemistry of Theonezolides A-C : Determination of the Absolute Stereochemistry of the C-4-C-17 Fragment" Tetrahedron. 54 (in press). (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] M.Ishibashi: "Studies on the Macrolides from Marine Dinoflagellate Amphidinium sp.:Structures of Amphidinolides R and S and a Succinate Feeding Experiment" Tetrahedron. 53. 7827-7832 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] M.Ishibashi: "Amphidinolides:Unique Macrolides from Marine Dinoflagellates" Heterocycles. 44. 543-572 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] J.Kobayashi: "Studies on the Stereochemistry of Theonezolides A〜C:Elucidation of the Relative Configurations of 1,3-Diol Moieties of the C-4〜C-17 Fragment" Heterocycles. 47(印刷中). (1998)

    • Related Report
      1997 Annual Research Report
  • [Publications] M.Sato: "Studies on the Stereochemistry of Theonezolides A〜C:Determination of the Absolute Stereochemistry of the C-4〜C-17 Fragment" Tetrahedron. 54(印刷中). (1998)

    • Related Report
      1997 Annual Research Report
  • [Publications] J. Kobayashi: "Amphidinolide Q, a Novel 12-Membered Macrolide from the Cultured Marine Dinoflagellate Amphidinium sp." Tetrahedron Lett.37. 1449-1450 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] H. Ishiyama: "Studies on the Stereochemistry of Amphidinolides : Synthesis of a Diastereomer of the C-1^〜C-9 Fragment of Amphidinolide C" Chem. Pharm. Bull.44. 1819-1822 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] M. Ishibashi: "Amphidinolides O and P, Novel 15-Membered Macrolides from the Dinoflagellate Amphidinium sp. : Analysis of the Relative Stereochemistry and Stable Solution Conformation" Journal of Organic Chemistry. 60. 6062-6066 (1995)

    • Related Report
      1995 Annual Research Report

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Published: 1996-04-01   Modified: 2016-04-21  

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