Design, synthesis and biological evaluation of novel stilbene-based antitumor agents

Bioorg Med Chem. 2009 Jan 15;17(2):512-22. doi: 10.1016/j.bmc.2008.12.002. Epub 2008 Dec 9.

Abstract

A series of novel stilbene derivatives has been synthesized and studied with the main goal to investigate SAR of the amino compound 1a, as well as to improve its water solubility, a potentially negative aspect of the molecule that could be a serious obstacle for a pre-clinical development. We have obtained derivatives with good cytotoxic activity, in particular, the derivatives 5c and 6b could represent two novel leads for further investigation. Compound 8b, a morpholino-carbamate derivative, prodrug of 1a, has a very good solubility in water, and is active in suppressing growth of tumor cells at a concentration of 5000 nM, which is a concentration 100 times higher than the parent stilbene 1a.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Dose-Response Relationship, Drug
  • Drug Design
  • Humans
  • Prodrugs / chemistry
  • Solubility
  • Stilbenes / chemical synthesis*
  • Stilbenes / pharmacology
  • Structure-Activity Relationship
  • Tubulin / metabolism

Substances

  • Amines
  • Antineoplastic Agents
  • Prodrugs
  • Stilbenes
  • Tubulin