Study on anti-proliferative effect of benzoxathiole derivatives through inactivation of NF-κB in human cancer cells

Bioorg Med Chem Lett. 2012 Jul 15;22(14):4523-7. doi: 10.1016/j.bmcl.2012.06.001. Epub 2012 Jun 7.

Abstract

To investigate the anti-proliferative effect of a newly discovered NF-kB inhibitor, 6,6-dimethyl-2-(phenylimino)-6,7-dihydrobenzo[d][1,3]oxathiol-4(5H)-one (1a), a series of its analogs (1b-n) were prepared and evaluated for their NF-κB inhibition and anti-proliferative activity against various human cancer cell lines. Slight variation of hydrophobicity by replacement of dimethyl group of 1a at 6-position with bulky isopropyl group and introduction of para-fluoro substitution on 2-phenyl group showed good NF-κB inhibitory activity and anti-proliferative activity. However, excessive increase in hydrophobicity with 2,4,6-trichloro substituents on phenyl group resulted in the loss of both the activities. From the SAR results, 2-phenylimino-6,7-dihydrobenzo[d][1,3]oxathiol-4(5H)-one was identified as the lead scaffold for investigating new anticancer agent through inactivation of NF-κB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzene Derivatives / chemical synthesis*
  • Benzene Derivatives / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Humans
  • Molecular Structure
  • NF-kappa B / antagonists & inhibitors*
  • Structure-Activity Relationship
  • Sulfhydryl Compounds / chemistry*
  • Sulfhydryl Compounds / pharmacology

Substances

  • Benzene Derivatives
  • NF-kappa B
  • Sulfhydryl Compounds