Synthesis and cytotoxicity of dihydroartemisinin ethers containing cyanoarylmethyl group

Bioorg Med Chem. 2003 Mar 20;11(6):977-84. doi: 10.1016/s0968-0896(02)00538-2.

Abstract

A new type of ether of dihydroartemisinin containing cyano and aryl groups was prepared and tested for cytotoxicity to A549, P388, L1210 and HT29 cells using the MTT assay. 12k and 12l were the most cytotoxic compounds. 13 lacking the peroxy group showed a 1000-fold less potency than 12l. Similarly, the inactive compound 14 indicated that the position of cyano groups was also important. Flow cytometry data showed that the compounds caused an accumulation of P388 cells in the G(1)-phase of the cell cycle.

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / chemical synthesis*
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Artemisia / chemistry
  • Drug Screening Assays, Antitumor
  • Ethers / chemical synthesis*
  • Ethers / pharmacology*
  • Flow Cytometry
  • G1 Phase / drug effects
  • HT29 Cells
  • Humans
  • Leukemia L1210 / drug therapy
  • Leukemia L1210 / pathology
  • Leukemia P388 / drug therapy
  • Leukemia P388 / pathology
  • Mice
  • Nitriles / chemical synthesis*
  • Nitriles / pharmacology*
  • Tetrazolium Salts
  • Thiazoles

Substances

  • Antineoplastic Agents, Phytogenic
  • Ethers
  • Nitriles
  • Tetrazolium Salts
  • Thiazoles
  • thiazolyl blue