Synthesis and antitumor activity of novel C-8 ester derivatives of leinamycin

Bioorg Med Chem Lett. 2003 Feb 10;13(3):455-8. doi: 10.1016/s0960-894x(02)00949-6.

Abstract

A novel series of C-8 ester derivatives of leinamycin are described. Condensation of N-substituted amino acids or carboxylic acids containing polyether moiety with leinamycin resulted in the C-8 ester derivatives with good antitumor activity in several experimental models. Among these derivatives, compound 4e, which has five ethylene glycol ether units in the C-8 acyl group, showed potent antitumor activity against human tumor xenograft. Combination with the modification of the dithiolanone moiety was applied to these C-8 ester derivatives and some of them also showed good antitumor activity.

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / chemical synthesis*
  • Antibiotics, Antineoplastic / pharmacology*
  • Cell Division / drug effects
  • Esters / chemical synthesis
  • Esters / pharmacology
  • HeLa Cells
  • Humans
  • Lactams*
  • Leukemia P388 / drug therapy
  • Macrolides
  • Mice
  • Mice, Nude
  • Sarcoma 180 / drug therapy
  • Structure-Activity Relationship
  • Thiazoles*
  • Thiones*

Substances

  • Antibiotics, Antineoplastic
  • Esters
  • Lactams
  • Macrolides
  • Thiazoles
  • Thiones
  • leinamycin