Skip to content
2000
Volume 16, Issue 8
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

Abstract

Design and discovery of new classes of anticancer agents with unique mechanisms of action is an urgent medical need. During the past several years, a series of salicylhydrazide class of compounds were reported to possess remarkable potency in a large panel of cancer cell lines from different tumor origins. In particular, the optimized lead compound, SC144, was further investigated and selected as a valuable drug candidate endowed with favorable pharmacokinetic and antiproliferative properties in various in vitro and in vivo xenograft models. This lead compound is active in cells resistant to conventional chemotherapies, synergistic with several standard-of-care drugs, and possesses an unique mechanism acting through the inhibition of the gp130-STAT3-survivin axis. Because of this novel mechanism, clinical development of SC144 will provide new therapeutic options for diverse cancers.

Loading

Article metrics loading...

/content/journals/mrmc/10.2174/138955751608160307175649
2016-05-01
2025-10-15
Loading full text...

Full text loading...

/content/journals/mrmc/10.2174/138955751608160307175649
Loading

  • Article Type:
    Research Article
Keyword(s): Anticancer agents; cytotoxicity; gp130; hydrazides; IL-24; pyrroloquinoxaline; survivin
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test