Synthesis and cytotoxicity study of alkannin derivatives

Eur J Med Chem. 2004 Sep;39(9):755-64. doi: 10.1016/j.ejmech.2004.05.004.

Abstract

Alkannin derivatives (3-19) were prepared through the reaction of beta,beta-dimethylacrylalkannin (1), the most abundant isohexenylnaphthazarin isolated from the roots of Arnebia euchroma, with different types of nucleophiles such as amines and thiols in the absence or presence of a reducing agent. The cytotoxicities of 1-8, 10-14 and 19 against four human carcinoma cell line (GLC-82, CNE2, Bel-7402, K-562) were found to be markedly higher than that of the naturally occurring beta,beta-dimethylacrylalkannin (1) and acetylalkannin (2). This study also shed light on the understanding of the biological activities in terms of the chemical reactivity of alkannins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boraginaceae / chemistry
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Drug Screening Assays, Antitumor
  • Humans
  • Molecular Structure
  • Naphthoquinones / chemical synthesis*
  • Naphthoquinones / chemistry
  • Naphthoquinones / pharmacology*
  • Structure-Activity Relationship

Substances

  • Naphthoquinones
  • alkannin
  • naphthazarin