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  • 标题:A common pharmacophore for cytotoxic natural products that stabilize microtubules
  • 本地全文:下载
  • 作者:Iwao Ojima ; Subrata Chakravarty ; Tadashi Inoue
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:1999
  • 卷号:96
  • 期号:8
  • 页码:4256-4261
  • DOI:10.1073/pnas.96.8.4256
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Taxol (paclitaxel), a complex diterpene obtained from the Pacific yew, Taxus brevifolia, is arguably the most important new drug in cancer chemotherapy. The mechanism of cytotoxic action for paclitaxel--i.e., the stabilization of microtubules leading to mitotic arrest--is now shared by four recently identified natural products, eleutherobin, epothilones A and B, and discodermolide. Their ability to competitively inhibit [3H]paclitaxel binding to microtubules strongly suggests the existence of a common binding site. Recently, we have developed nonaromatic analogues of paclitaxel that maintain high cytotoxicity and tubulin binding (e.g., nonataxel). We now propose a common pharmacophore that unites paclitaxel, nonataxel, the epothilones, eleutherobin, and discodermolide, and rationalizes the extensive structure-activity relationship data pertinent to these compounds. Insights from the common pharmacophore have enabled the development of a hybrid construct with demonstrated cytotoxic and tubulin-binding activity.
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