4'-Alkoxyl substitution enhancing the anti-mitotic effect of 5-(3',4',5'-substituted)anilino-4-hydroxy-8-nitroquinazolines as a novel class of anti-microtubule agents

Bioorg Med Chem Lett. 2006 Nov 15;16(22):5864-9. doi: 10.1016/j.bmcl.2006.08.058. Epub 2006 Aug 30.

Abstract

Mitosis inhibitors are powerful anticancer drugs. Based on a novel anti-microtubule agent of 5-(4'-methoxy)anilino-4-hydroxy-8-nitroquinazoline, a series of 5-(3',4',5'-substituted)anilino-4-hydroxy-8- nitroquinazolines were designed and synthesized to investigate the effect of the substitution on the inhibitory activity against mitotic progression of tumor cells. The large alkoxyl substitution on the 4'-position of 5-anilino ring is beneficial for the potency. The 5-(3',4',5'-trimethoxy)anilino-8-nitroquinazoline (1h) displays an overwhelming activity in arresting the cells at the G2/M phase, providing a promising new template for further development of potent microtubule-targeted anti-mitotic drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemistry*
  • Aniline Compounds / chemical synthesis*
  • Aniline Compounds / pharmacology*
  • Antimitotic Agents / pharmacology*
  • Cell Division / drug effects
  • Cell Division / physiology
  • Cell Line, Tumor
  • G2 Phase / drug effects
  • G2 Phase / physiology
  • Humans
  • Microtubules / drug effects*
  • Mitosis / drug effects*
  • Mitosis / physiology
  • Quinazolines / chemical synthesis*
  • Quinazolines / pharmacology*
  • Structure-Activity Relationship

Substances

  • Alcohols
  • Aniline Compounds
  • Antimitotic Agents
  • Quinazolines
  • alkoxyl radical