Structures and cytotoxic properties of trichoverroids and their macrolide analogues produced by saltwater culture of Myrothecium verrucaria

J Med Chem. 2003 Sep 25;46(20):4342-50. doi: 10.1021/jm030090t.

Abstract

Saltwater culture of Myrothecium verrucaria, separated from a Spongia sp. collected in Hawaii, was a source of three new trichothecenes, 3-hydroxyroridin E (1a), 13'-acetyltrichoverrin B (2), and miophytocen C (3) and nine known related compounds (1b, 4, 5, 6, 7a, 7b, 8, 9a, and 9b). The stereostructures of the new compounds were established on the basis of 1D and 2D NMR spectral analyses and a chemical transformation. At the same time, the stereostructures of known compounds, 1b, 4, and 5 reported previously were also elucidated. All the compounds except 3 showed significant cytotoxicity against murine and human tumor cell lines. Moreover, the structure-activity relationships (SARs) were established from the results of the bioassay data.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / isolation & purification
  • Antineoplastic Agents / pharmacology*
  • Basidiomycota / chemistry*
  • Basidiomycota / metabolism
  • Bone Marrow Cells / drug effects
  • Drug Screening Assays, Antitumor
  • Humans
  • Lethal Dose 50
  • Macrolides / chemistry*
  • Macrolides / isolation & purification
  • Macrolides / pharmacology*
  • Mice
  • Nuclear Magnetic Resonance, Biomolecular
  • Stereoisomerism
  • Trichothecenes / chemistry*
  • Trichothecenes / isolation & purification
  • Trichothecenes / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Macrolides
  • Trichothecenes