Potential antitumor agents. 24. Synthesis and pharmacological behavior of imidazo[2,1-b]thiazole guanylhydrazones bearing at least one chlorine

J Med Chem. 1996 Jul 5;39(14):2852-5. doi: 10.1021/jm9509307.

Abstract

In connection with a previous research dealing with the antitumor activity of imidazo[2,1-b]-thiazole guanylhydrazones, this paper reports the synthesis of new derivatives which were tested for antitumor and positive inotropic activity. In most cases the cytotoxic data from the in vitro experiments (HeLa) were in agreement with the antitumor data in vivo (Ehrlich). The active compounds bear a phenyl ring at the 6 position. On the other hand, the most active cardiotonic agents were devoid of the phenyl ring.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Carcinoma, Ehrlich Tumor / drug therapy
  • Cardiotonic Agents / chemical synthesis*
  • Cardiotonic Agents / pharmacology
  • Chlorine
  • Drug Screening Assays, Antitumor
  • Female
  • HeLa Cells
  • Humans
  • Hydrazones / chemical synthesis*
  • Hydrazones / pharmacology
  • Mice
  • Structure-Activity Relationship
  • Thiazoles / chemical synthesis*
  • Thiazoles / pharmacology

Substances

  • Antineoplastic Agents
  • Cardiotonic Agents
  • Hydrazones
  • Thiazoles
  • Chlorine