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Journal of Wood Science

Official Journal of the Japan Wood Research Society

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Chemical constituents ofInonotus obliquus II: a new triterpene, 21,24-cyclopentalanosta-3β,21,25-triol-8-ene from sclerotium

Journal of Wood Science volume 47, pages 313–316 (2001)Cite this article

Abstract

A new lanostane-type triterpene with a cyclopentanol partial structure in the side chain was isolated from the sclerotium of the wood rotting fungusInonotus obliquus along with four known compounds: lanosterol, inotodiol, trametenolic acid, and 3β-hydroxy-8,24-dienlanosta-21,23-lactone. The new compound was determined to be 21,24-cyclopentalanosta-3β,21,25-triol-8-ene by spectroscopic analyses.

References

  1. Yamaguchi T (1992) Basidiosphore discharge ofFuscoporia obliqua (in Japanese). Ringakkai Hokkaido Sibu Ronbunshu 40:30–32

    Google Scholar 

  2. Molitoris HP (1994) Mushrooms in medicine. Folia Microbiol 39(2):91–98

    Article  CAS  Google Scholar 

  3. Maret S (1991) Fungi in Khanty folk medicine. J Ethnopharmacol 31:175–179

    Article  Google Scholar 

  4. Mizuno T, Zhuang C, Abe K, Okamoto H, Kiho T, Ukai S, Leclerc S, Meijer L (1996) Studies on the host-mediated antitumor polysaccharides. Part XXVII. Mushroom Sci Biotechnol 3(2):53–60

    Google Scholar 

  5. Kahlos K, Kangas L, Hiltunen R (1987) Antitumour activity of some compounds and fractions from ann-hexane extract ofInonotus obliquus. Acta Pharm Fenn 96:33–40

    CAS  Google Scholar 

  6. Shin Y, Tamai Y, Terazawa M (2000) Chemical constituents ofInonotus obliquus I. Eurasian J For Res 1:43–50

    CAS  Google Scholar 

  7. Kahlos K, Schantz MV, Hiltunen R (1984) 3β-Hydroxy-lanosta-8,24-dien-21-al, a new triterpene fromInonotus obliquus. Acta Pharm Fenn 92:197–198

    Google Scholar 

  8. Kahlos K, Hiltunen R (1986) Two oxygenated lanostane type triterpenes fromInonotus obliquus. Acta Pharm Fenn 95:71–76

    CAS  Google Scholar 

  9. Kahlos K (1986) 3β,22-Dihydroxy-lanosta-8,24-dien-7-one, a new 7-keto compound fromInonotus obliquus. Acta Pharm Fenn 95:113–117

    CAS  Google Scholar 

  10. Kahlos K, Hiltunen R (1986) 3β,22-Dihydroxy-lanosta-7,9(ll),24-trien, a new minor compound fromInonotus obliquus. Planta Med 52:495–496

    Article  Google Scholar 

  11. Kahlos K, Kangas L, Hiltunen R (1986) Antitumour tests of inotodiol from the fungus.Inonotus obliquus. Acta Pharm Fenn 95:173–177

    Google Scholar 

  12. Gninenko YI (1995) On the problem of the stock of the fungusInonotus obliquus (PERS.)Pil.F. sterilis(VAN)NIKOL: in northern and central Kazakhstan. Rastitel Nye Resursy 31(4):37–40

    Google Scholar 

  13. Burczyk J, Gawrin A, Slotwinska M (1996) Antimitotic activity of aqueous extracts ofInonotus obliquus. Bull Chim Farmaceut Anno 135:306–309

    CAS  Google Scholar 

  14. Kahlos K, Lesnau A, Lange W, Lindequist U (1996) Preliminary tests of antiviral activity of twoInonotus obliquus strains. Fitoterapia 67:344–347

    Google Scholar 

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Authors and Affiliations

  1. Laboratory of Forest Chemistry, Research Group of Forest Resource Science, Division of Environment Resource, Faculty of Agriculture, Hokkaido University, 060-8589, Sapporo, Japan

    Yusoo Shin, Yutaka Tamai & Minoru Terazawa

Authors
  1. Yusoo Shin
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  2. Yutaka Tamai
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  3. Minoru Terazawa
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Correspondence to Yusoo Shin.

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Shin, Y., Tamai, Y. & Terazawa, M. Chemical constituents ofInonotus obliquus II: a new triterpene, 21,24-cyclopentalanosta-3β,21,25-triol-8-ene from sclerotium. J Wood Sci 47, 313–316 (2001). https://doi.org/10.1007/BF00766719

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  • DOI: https://doi.org/10.1007/BF00766719

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