Published January 1, 2017 | Version v1
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Synthesis and Topoisomerase I inhibitory properties of klavuzon derivatives

  • 1. Izmir Inst Technol, Fac Sci, Dept Chem, TR-35430 Izmir, Turkey
  • 2. Izmir Inst Technol, Fac Sci, Dept Mol Biol & Genet, TR-35430 Izmir, Turkey
  • 3. Ege Univ, Fac Engn, Dept Bioengn, Canc Biol Lab, Izmir, Turkey

Description

Klavuzon is a naphthalen-1-yl substituted alpha,beta-unsaturated delta-lactone derivative, and is one of the antiproliferative members of this class of compounds. Asymmetric and racemic syntheses of novel alpha,beta unsaturated delta-lactone derivatives are important to investigate their potential for the treatment of cancer. In this study, asymmetric and racemic syntheses of heteroatom-substituted klavuzon derivatives are reported. The syntheses were completed by a well-known three-step procedure. Anti-proliferative activity of seven novel racemic klavuzon derivatives were reported against MCF-7, PC3, HCT116 p53+/+ and HCT116 p53-/- cancer cell lines. Topoisomerase I inhibitory properties of 5,6-dihydro-2H-pyran-2-one derivatives were also studied. (C) 2017 Elsevier Inc. All rights reserved.

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