Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives

Bioorg Med Chem. 2012 May 1;20(9):3016-30. doi: 10.1016/j.bmc.2012.03.001. Epub 2012 Mar 15.

Abstract

Two cucurbitacins, dihydrocucurbitacin B (1) and cucurbitacin B (2), which can be obtained in large amounts from the roots of Wilbrandia ebracteata and from the fruits of Luffa operculata, respectively, were used as starting materials for the preparation of a library of 29 semi-synthetic derivatives. The structural changes that were performed include the removal, modification or permutation of functional groups in rings A and B as well as in the side chain. All new semisynthetic compounds, as well as 1 and 2, were tested in vitro for their cytotoxic effects on non-small-cell lung cancer cells (A549 cells). Some of these compound displayed potent to moderate activity against A549 tumor cells, especially those cucurbitacin B derivatives which were modified at ring A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / toxicity*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cucurbitaceae / chemistry
  • Fruit / chemistry
  • Humans
  • Luffa / chemistry
  • Plant Roots / chemistry
  • Triterpenes / chemical synthesis
  • Triterpenes / chemistry*
  • Triterpenes / toxicity*

Substances

  • Antineoplastic Agents
  • Triterpenes
  • dihydrocucurbitacin B
  • cucurbitacin B