Synthesis of sex hormone-derived modified steroids possessing antiproliferative activity

被引:56
作者
Frank, Eva [1 ]
Schneider, Gyula [1 ]
机构
[1] Univ Szeged, Dept Organ Chem, H-6720 Szeged, Hungary
基金
匈牙利科学研究基金会;
关键词
Steroid; Modified sex hormones; Synthesis; Antiproliferative activity; IN-VITRO; ANTIMITOTIC ACTIVITY; RECEPTOR-BINDING; 2-METHOXYESTRADIOL ANALOGS; STEREOSELECTIVE-SYNTHESIS; BIOLOGICAL EVALUATION; AROMATASE INHIBITORS; CYTOTOXIC ACTIVITY; EFFICIENT APPROACH; BREAST-CANCER;
D O I
10.1016/j.jsbmb.2013.02.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During recent years intensive research has been focused on the synthesis of structurally modified steroid hormones in order to obtain compounds with beneficial biological activity such as cell-growth inhibition. Experimental results have revealed that some steroidal derivatives possess direct cytostatic effect on cancer cells in a hormone receptor-independent manner. After a brief account on the most important biological function and characteristics of the naturally occurring sex hormones in physiological and pathological conditions, structural modifications of estrane and androstane scaffolds are discussed in detail. The review covers literature publications (from 2002 to 2012) relating to the synthesis and antiproliferative activity of semisynthetic sex hormone-derived molecules containing simple or heterocyclic substituents. The compounds reviewed are divided into three main categories according to their sterane framework and the nature of substitution. This article is part of a Special Issue entitled "Synthesis and biological testing of steroid derivatives as inhibitors". (C) 2013 Published by Elsevier Ltd.
引用
收藏
页码:301 / 315
页数:15
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