Cytotoxicity of new pyrazino[1,2-b]isoquinoline and 6,15-iminoisoquino[3,2-b]3-benzazocine compounds

Bioorg Med Chem. 2010 Sep 15;18(18):6813-21. doi: 10.1016/j.bmc.2010.07.049. Epub 2010 Jul 25.

Abstract

Looking for optimised analogues of compound 2 that might be useful in colon cancer therapy, we here explore the in vitro cytotoxicity against MDA-MB 231 human breast carcinoma, A-549 human lung carcinoma and HT-29 human colon carcinoma cell lines of several analogues and derivatives. The effect of the R2-substituent and/or the introduction of an arylmethyl side-chain at C-3, as well as the presence of a double bond in the skeleton or a methoxy group at C-1 have been investigated. New 6,15-iminoisoquino[3,2-b]3-benzazocine compounds, related to the saframycin family, in which the C(7)-N(8)-C(9)-substructure contains a lactam function, a fused oxazolidine or an aminonitrile function were also studied, and many of them showed low micromolar GI50 values.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / toxicity
  • Azocines / chemical synthesis
  • Azocines / chemistry*
  • Azocines / toxicity
  • Cell Line, Tumor
  • Humans
  • Isoquinolines / chemical synthesis
  • Isoquinolines / chemistry*
  • Isoquinolines / toxicity
  • Pyrazines / chemical synthesis
  • Pyrazines / chemistry*
  • Pyrazines / toxicity
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Azocines
  • Isoquinolines
  • Pyrazines
  • isoquinoline