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. 1985 Nov;50(5):1225–1228. doi: 10.1128/aem.50.5.1225-1228.1985

7 alpha-hydroxytrichodermol, a new trichothecene from Myrothecium roridum.

B B Jarvis, Y W Lee, C S Yatawara, D B Mazzocchi, J L Flippen-Anderson, R Gilardi, C George
PMCID: PMC238729  PMID: 4091555

Abstract

Five plant-pathogenic isolates of Myrothecium roridum from Florida produced only simple trichothecenes rather than the usual macrocyclic trichothecenes. The major metabolite was 7 alpha-hydroxytrichodermol.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Kupchan S. M., Streelman D. R., Jarvis B. B., Dailey R. G., Jr, Sneden A. T. Isolation of potent new antileukemic trichothecenes from Baccharis megapotamica. J Org Chem. 1977 Dec 23;42(26):4221–4225. doi: 10.1021/jo00862a011. [DOI] [PubMed] [Google Scholar]
  2. Lee Y. W., Mirocha C. J. Production of Nivalenol and Fusarenone-X by Fusarium tricinctum Fn-2B on a Rice Substrate. Appl Environ Microbiol. 1984 Oct;48(4):857–858. doi: 10.1128/aem.48.4.857-858.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. McDougal P. G., Schmuff N. R. Chemical synthesis of the trichothecenes. Fortschr Chem Org Naturst. 1985;47:153–219. doi: 10.1007/978-3-7091-8790-6_3. [DOI] [PubMed] [Google Scholar]
  4. Schuda P. F., Potlock S. J., Wannemacher R. W., Jr Trichothecenes, 1: The synthesis of 4-deoxyverrucarol from verrucarol and diacetoxyscirpenol. J Nat Prod. 1984 May-Jun;47(3):514–519. doi: 10.1021/np50033a019. [DOI] [PubMed] [Google Scholar]

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