Synthesis of isosteric selenium analog of the PPARβ/δ agonist GW501516 and comparison of biological activity

Arun K. Sharma, Ugir Hossain Sk, Pengfei He, Jeffrey M. Peters, Shantu Amin

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors and members of the nuclear hormone receptor superfamily. Herein, we describe an efficient synthesis of a novel isosteric selenium analog of the highly specific PPARβ/δ ligand 2-methyl-4-((4-methyl-2-(4-trifluoromethylphenyl)-1,3-thiazol-5-yl)-meth ylsulfanyl)phenoxy-acetic acid (GW501516; 1). The study examined the efficiency of the novel selenium analog 2-methyl-4-((4-methyl-2-(4-trifluoromethylphenyl)-1,3-selenazol-5-yl)-me thylsulfanyl)phenoxy-acetic acid (2) to activate PPARβ/δ and the effect of ligand activation of PPARβ/δ on cell proliferation and target gene expression in human HaCaT keratinocytes. The results showed that similar to GW501516, the Se-analog 2 increased expression of the known PPARβ/δ target gene angiopoietin-like protein 4 (ANGPTL4); the compound 2 was comparable in efficacy as compared to GW501516. Consistent with a large body of evidence, the Se-analog inhibited cell proliferation in HaCaT keratinocytes similar to that observed with GW501516. In summary, the novel Se-analog 2 has been developed as a potent PPARβ/δ ligand that may possess additional anti-cancer properties of selenium.

Original languageEnglish (US)
Pages (from-to)4050-4052
Number of pages3
JournalBioorganic and Medicinal Chemistry Letters
Volume20
Issue number14
DOIs
StatePublished - Jul 15 2010

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Pharmaceutical Science
  • Drug Discovery
  • Clinical Biochemistry
  • Organic Chemistry

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