Structure-activity profiles of eleutherobin analogs and their cross-resistance in Taxol-resistant cell lines

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Cancer Chemotherapy and Pharmacology

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1007/s002800050957PMID 10412947
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Characterization of the Taxol Binding Site on the Microtubule

  1999cited by this paper
• The Total Synthesis of Eleutherobin

  1999cited by this paper
• A CONVERGENT ROUTE FOR THE TOTAL SYNTHESIS OF THE ELEUTHESIDES

  1998cited by this paper
• Eleutherobin, a novel cytotoxic agent that induces tubulin polymerization, is similar to paclitaxel (Taxol).

  1998cited by this paper
• Mechanisms of Taxol-induced cell death are concentration dependent.

  1998cited by this paper
• The Total Synthesis of Eleutherobin: A Surprise Ending.

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  1998cited by this paper
• Eleutherobin, a New Cytotoxin that Mimics Paclitaxel (Taxol) by Stabilizing Microtubules.

  1997cited by this paper
• Taxol induces tyrosine phosphorylation of SHC and its association with GRB2 in murine raw 264.7 cells

  1997cited by this paper
• Taxol-resistant epithelial ovarian tumors are associated with altered expression of specific beta-tubulin isotypes.

  1997cited by this paper
• SYNTHESIS OF THE TRICYCLIC CORE OF ELEUTHEROBIN AND SARCODICTYINS AND TOTAL SYNTHESIS OF SARCODICTYIN A

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