Synthesis and Topoisomerase I inhibitory properties of klavuzon derivatives
Makaleler > Tam Makale · 2017
Yazarlar: Ismail Akcok, Derya Mete, Ayhan Sen, Pinar Kasaplar, Kemal Sami KORKMAZ, Ali Cagir
Bioorganic Chemistry, SCI Expanded İndekslerine Giren Dergi, Uluslararası, Wos, 2017, cilt 71, ss 275-284
DOI: 10.1016/j.bioorg.2017.02.012
Özet
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.