Publication Cover
Xenobiotica
the fate of foreign compounds in biological systems
Volume 20, 1990 - Issue 7
24
Views
15
CrossRef citations to date
0
Altmetric
Original Article

Metabolism of illudin S, a toxic principle of Lampteromyces japonicus, by rat liver. I. Isolation and identification of cyclopropane ring-cleavage metabolites

, , &
Pages 671-681 | Received 14 Sep 1989, Accepted 02 Mar 1990, Published online: 27 Aug 2009

References

  • Bax A. Two-dimensional NMR in Liquids. D. Reidel, Holland 1982
  • Benn R., Günther H. Modern pulse methods in high-resolution NMR spectroscopy. Angewante Chemie (international edition in English) 1983; 22: 350–380
  • Brady S. F., Ilton M. A., Johnson W. S. A high stereoselective synthesis of transtrisubstituted olefinic bonds. Journal of the American Chemical Society 1968; 90: 2882–2889
  • Fukuda K., Uematsu T., Hamada A., Akiya S., Komatsu N., Okubo A. The polysaccharide from Lampteromyces japonicus. Chemical Pharmaceutical Bulletin 1975; 23: 1955–1959
  • Ichihara A., Shirahama H., Matsumoto T. Dihydroilludin S, a new constituent from Lampteromyces japonicus. Tetrahedron Letters 1969; 45: 3965–3968
  • Itano T. Illudin S; a possible new type inhibitor of RNA synthesis, and analysis of its action mechanism. Okayama Igaku Zasshi 1978; 91: 453–460
  • Kelner M. J., McMorris T. C., Beck W. T., Zamora J. M., Taetle R. Preclinical evaluation of illudin S as anticancer agents. Cancer Research 1987; 47: 3186–3189
  • Matsumoto T., Shirahama H., Ichihara A., Fukuoka Y., Takahashi Y., Mori Y., Watanabe M. Structure of lampterol (illudin S). Tetrahedron 1965; 21: 2671–2676
  • Nakanishi K., Ohashi M., Suzuki N., Tada M., Yamada Y., Inagaki S. Isolation of lampterol from Lampteromyces japonicus (KAWAM.) SING. Yakugaku Zasshi 1963; 83: 377–380
  • Nakanishi K., Tada M., Yamada Y., Ohashi M., Komatsu N., Terakawa H. Isolation of lampterol, an antitumour substance from Lampteromyces japonicus. Nature 1963 b; 197: 292
  • Nakanihsi K., Tada M., Yamada Y. Stereochemistry of illudin-S (lampterol). Chemical Pharmaceutical Bulletin 1964; 12: 856–857
  • Nakanishi K., Ohashi M., Tada M., Yamada Y. Illudin S (lampterol). Tetrahedron 1965; 21: 1231–1246
  • Neidleman S. L., Geigert J. Biohalogenation: Principles, Basic Roles and Applications. Ellis Horwood, Chichester 1986
  • Peter A., Bredshaw W., Hanson J. R., Sadler I. H. Studies in terpenoid biosynthesis. Part 26. Applications of 2H and 13C n.m.r. spectroscopy to the biosynthesis of the illudin sesquiterpenoids. Journal of the Chemical Society Perkin Transactions, I 1982; 10: 2445–2448
  • Shinozawa K., Tsutsui K., Oda T. Enhancement of the effect of illudin S by including it into liposomes. Experientia 1979; 35: 1102–1103
  • Suckling C. J. The cyclopropyl group in studies of enzyme mechanism and inhibition. Angewante Chemie (international edition in English) 1988; 27: 537–552
  • Tada M., Yamada Y., Bhacca N. S., Nakanishi K., Ohashi M. Structure and reactions of illudin S (lampterol). Chemical Pharmaceutical Bulletin 1964; 12: 853–855
  • Tsuda R., Kawano M., Hara M. Phytohemagglutinin found in Lampteromyces japonicus. Igakukenkyu 1986; 56: 22–26

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.