Furoxan derivatives as cytotoxic agents: preliminary in vivo antitumoral activity studies

Pharmazie. 2006 Jan;61(1):54-9.

Abstract

Furoxan derivatives with in vitro cytotoxic activity were investigated as antitumoral agents in vivo. The compounds were tested in murine models of both CCRFS-180 II sarcoma and mammary adenocarcinoma. Two of the furoxan derivatives considered here, 3-formyl-4-phenyl-1,2,5-oxadiazole N2-oxide and 3-carbonitrile-4-phenyl-1,2,5-oxadiazole N2-oxide, present in vivo antitumoral activity. They were able to produce more than 90% of tumoral necrosis under the experimental protocol of administration and posology employed. NO-releasing capacity of furoxans may explain the anti-neoplastic activity of these compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / toxicity
  • Cell Line, Tumor
  • Chemical Phenomena
  • Chemistry, Pharmaceutical
  • Chemistry, Physical
  • Female
  • Mammary Neoplasms, Experimental / drug therapy
  • Mammary Neoplasms, Experimental / pathology
  • Mice
  • Mice, Inbred BALB C
  • Neoplasm Transplantation
  • Oxadiazoles / chemical synthesis*
  • Oxadiazoles / pharmacology*
  • Oxadiazoles / toxicity
  • Quinoxalines / pharmacology
  • Sarcoma, Experimental / drug therapy
  • Sarcoma, Experimental / pathology

Substances

  • Antineoplastic Agents
  • Oxadiazoles
  • Quinoxalines
  • furoxans
  • quindoxin