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Antitumor components from an actinomycete strain 6011W.

Abstract
Three bioactive compounds that inhibited nucleoside transport were isolated from the cultured broth of Streptoverticillium sp. 6011W. The structures of those compounds were characterized as cinnamamide, N-(tetrahydro-2-oxo-3-thienyl)-acetamide and benzamide, respectively. They all inhibited radiolabeled thymidine transport into Ehrlich carcinoma cells, with IC50 values of 30.4, 97.2 and 85.4 microM, respectively. When administered i.p., cinnamamide not only inhibited the growth of transplanted tumors but also reduced the number of lung metastases in mice bearing Lewis lung carcinoma. The results suggest that nucleoside transport inhibition assay is a valuable model to search for antitumor agents of natural origin.
AuthorsX F Jiang, B Y Shang, L F Jin, J L Hu, Y S Zhen
JournalJournal of Asian natural products research (J Asian Nat Prod Res) Vol. 2 Issue 1 Pg. 31-8 ( 1999) ISSN: 1028-6020 [Print] England
PMID11261203 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
Topics
  • Actinomycetales (chemistry)
  • Animals
  • Antineoplastic Agents (chemistry, isolation & purification, pharmacology)
  • Drug Screening Assays, Antitumor
  • Humans
  • Mice
  • Molecular Structure
  • Spectrum Analysis
  • Tumor Cells, Cultured

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