Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone
摘要:
Based on biological properties of epoxyquinols from natural sources, bromo and epoxyquinols derived from estrone were synthesized and screened against Fem-X. HeLa and K-562 cell lines. Evidence was found that the bromine atom and the epoxy moiety significantly increase the antiproliferative activity within the series. (C) 2001 Elsevier Science Ltd. All rights reserved.
Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds
作者:Dragana Milić、Tatjana Kop、Zorica Juranić、Miroslav J. Gašić、Bernard Tinant、Gabriella Pocsfalvi、Bogdan A. Šolaja
DOI:10.1016/j.steroids.2005.07.001
日期:2005.12
observed, followed by acid-catalyzed epoxy-ring opening and subsequent double bond migration, giving as a final product Delta(9,11)A-ring aromatized compounds. Synthesis of conduritol-like compounds and structure confirmation by X-ray crystallography of the precursor of steroidal conduritol is also described. In addition, the results of extensive antiproliferative screening against a panel of 60 cancer cell
Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone
作者:Dragana R. Milić、Tatjana Kop、Zorica Juranić、Miroslav J. Gašić、Bogdan A. Šolaja
DOI:10.1016/s0960-894x(01)00402-4
日期:2001.8
Based on biological properties of epoxyquinols from natural sources, bromo and epoxyquinols derived from estrone were synthesized and screened against Fem-X. HeLa and K-562 cell lines. Evidence was found that the bromine atom and the epoxy moiety significantly increase the antiproliferative activity within the series. (C) 2001 Elsevier Science Ltd. All rights reserved.