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2001 Fiscal Year Final Research Report Summary

NOVEL METHOD FOR THE PRODUCTION OF TAXANE DITERPENES

Research Project

Project/Area Number 10555320
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field Synthetic chemistry
Research InstitutionNIIGATA UNIVERSITY

Principal Investigator

ANDO masayoshi  NIIGATA UNIVERSITY, Faculty of Engineering, Professor, 工学部, 教授 (40004402)

Co-Investigator(Kenkyū-buntansha) OTOMATSU Toshihiko  Kobe Natural Products & Chemiclas Co., Lts., Team Leader, Research & Development Dept., チームリーダー(研究職)
HIRATA Naonori  Kobe Natural Products & Chemicals Co., Ltd., manager, Research & Development Dept., 開発部長(研究職)
SUZUKI Todshio  NIIGATA UNIVERSITY, Faculty of Engineering, Professor, 工学部, 教授 (80202133)
Project Period (FY) 1998 – 2000
KeywordsTaxol / Taxus cuspidata / Taxane diterpene / Modulators of multidrug resistant tumor cells / P-糖蛋白質阻害剤 / 新規作用抗癌剤 / イチイカルス / タキソール生合成
Research Abstract

(1) Taxol, Taxol analogs, and New Basic and Neutral Taxoids from Taxus cuspidata
(a) We examined the content of taxol in needles and stems of Japanese yew, Taxuscuspidata grown in different 5 places in Japan, Sendai, Matumoto, Wakkanai, Asahikawa, and Toyotomi. The isolated yields of taxol are 0.0022%, 0.0006%, 0.0043%, 0.0033%, 0.0007% based on the weight of fresh needles and stems respectively. The results show that 25 Kg of fresh reproducible needles and stems of T. cuspidata grown in Wakkanai, produce 1 g of taxol. We also isolated new basic and neutral taxoids and determined their structures mainly by spectroscopic method.
(b) We examined biological activity of 42 taxoids as modulators of multidrug resistant cancer cells and found that 11 taxoids showed strong activity. In them taxinines NN-1 and NN-11 also showd anticancer activity in the screening assay by cell line panel, the results of which suggest that they are a new type of anticancer reagent.
(2) Production of Taxol, Taxol an … More alogs, Taxuyunnanine C and Its Related Compounds by Callus Culture of T. cuspidata. The Callus cultures induced from young stems of T. cuspidata grown in Sendai produce twxol, and 14 taxoids including 6 taxol analogs. The yield of taxol is 263 mg/1 Kg dry callus and the total yield of taxoids is 16.6 g/1 Kg dry callus. In them 5 kinds of taxoids, which are produced in excellent yields in callus cultures but not produced in the needles and stems, showed high activity as the modulator of multidrug resistant cancer cell. the yields and the kinds of products largely depend on additives and conditions.
(3)Partial Synthesis of Biologically, Active Taxoids. Since the very limited amount of biologically active taxinines NN-1, -3, -7, -14, and 5-cinnamoyl-10-acetoxy taxcin II were produced from natural sources, they were synthesized from taxinine, which is the most abundant product in needles and young stems of T. cuspidata, in good yoilds to keep enough amount of samples in vivo assay of these compounds. Less

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] 安東 政義: "Neutral taxoids from Taxus cuspidota as modulators of multidrug-resistant tumor cells"Phytochemisby. 54(8). 839-845 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 安東 政義: "Santonine-related compound 2 inhibits the expussion of ICAM-1 in response to IL-1 stimulation by blocking the signaling pathway upstream of IkB degradadon"Immunophurucology. 48. 129-135 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 安東 政義: "Two taxoids from Taxus cuspidata as modulators of multidrug resistant tumor cells"Heterocycles. 54(2). 999-1009 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 安東 政義: "Stereospecific Synthcsis of α,ω-cis-and α,ω-trans-Disubsututed Oxepanes"Tetrahedron Letters. 41(40). 7697-7700 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 安東 政義: "Cyclization of hydroxy epoxides promoted by (Bu_3Sn)_2O/Lewis acid: efficient synthesis of oxepanes"Tetrahedron Letters. 41(40). 7701-7704 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 安東 政義: "Application of Ring Closing Metathesis to the First Total Synthesis of (R)-(+)-Muscopyridine: Determination of Absolute Stereochemistry"Jounal of Organic Chemistry. 46. 7231-7234 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Jun-ichi Sakai, Hirofumi Sasaki, Katsuhiko Kosugi, Shuiun Zang, Naonori Hirata, Katutoshi Hirose, Akihiro Tomida, Takashi Tsurao, Masayoshi Ando: "Neutral taxoids from Taxus cuspidata as modulators of multidrug-resistant tumor cells"Heterocycles. 54(2). 999-1009 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Katsuhiko Kosugi, Jun-ichi Sakai, Shujun Zang, Yusuke Watanabe, EBrofumi Sasaki, Toshio Suzuki, Hisahiro Hagiwara, Naonori Hirata, Katutoshi Hirose, Masayoshi Ando, Akihiro Tomida, Takashi Tsunio: "Neutral taxoids from Taxus cuspidata as modulators of multidrag-resistant tumor cells"Phytochemistry. 54(8). 839-845 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shigeto Kawai, Takao Kataoka, Hikaru Sugimoto, Akito Nakamura, Takafumi Kobayashi, Kei Arao, Yohsuke Higuchi, Masayoshi Ando, Kazuo Nagai: "Santonine-related compound 2 inhibits the expression of ICAM-1 in response to IL-l stimulation by blocking the signaling pathway upstream of 1KB degradation"Immunopharmacclogy. 48. 129-135 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Saori Yuuya, Hisahiro Hagiwara, TosWo Suzuki Masavosi Ando. Atsusi Yamada, Kouj Suda, Takao Kataoka, Kazuo Nagai: "Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanrfiin, and Their Derivarives"J. Natural Products. 62(11). 22-30 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Fumito Shimoma, Haruhiko Kusaka, Hidenori Azami, Katsuaki Wada, Toshio Suzuki, Hisahiro Hagiwara, Masayosi Ando: "Total Synthesis of (±)-Hymenolin and (±)-Parthenin"Journal of Organic Chemistry. 63(11). 3758-3763 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] F. Shimoma, F. Kusaka, K. Wada, H. Azami, M. Yasunami, T. Suzuki, H. Hagiwara, M. Ando: "A Novel Synthetic Method of the (±)-(3aα,8aα)-Ethyl8β-Hydroxy-6β-methyl-2-oxooctahydro-2Η-cyclohepta[b] furan-3α-carboxylate and Its Chemical Transformation to (±)-(3aα,8aα)-3α,6β-Dimemyl-3 ,3a,4,5 ,6, 8a-hexahydro-2Η-cyclohepta[b] furan-2-one, (+)- and (-)-7β-(2-Acetoxy- 1α-methylemyl)-4β-memyl2-cyclohepten- 1β-o1, and (+)- and (-)-7β-{2-Acetoxy 1α-methylethyl)-4β-methyl-2-cyclohepten- l -one. Possible Common Synthetic Intermediate for Pseudoguaianolides, 4,5 -Secopseudoguaianolides, Guaianolides, 4,5-Secoguaianolides, and Octalactins."Journal of organic Chemistry. 63(4). 920-929 (1998)

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      「研究成果報告書概要(欧文)」より

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Published: 2003-09-17  

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