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The first synthesis of clausenamine-A and cytotoxic activities of three biscarbazole analogues against cancer cells.

Abstract
Clausemine-A (3), isolated from the stem and root bark of Clausena excavata, was synthesized using Suzuki cross-coupling and Oxidative coupling as the key step. Compound 3, and the other two structurally related biscarbazoles 1 and 2, showed potent cytotoxic activities against a variety of human cancer cell lines in vitro.
AuthorsA Zhang, G Lin
JournalBioorganic & medicinal chemistry letters (Bioorg Med Chem Lett) Vol. 10 Issue 10 Pg. 1021-3 (May 15 2000) ISSN: 0960-894X [Print] England
PMID10843207 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Carbazoles
  • clausenamine A
Topics
  • Antineoplastic Agents (chemical synthesis, pharmacology)
  • Carbazoles (chemical synthesis, pharmacology)
  • Drug Screening Assays, Antitumor
  • Humans
  • Tumor Cells, Cultured

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