Structural Modification for Antitumor Nitrogenous Steroids

被引:0
作者
Xie Tian-Peng [1 ]
Yang Kang [1 ]
Zhang Li-Zhi [1 ]
Chen De-Sheng [1 ]
Zou Kun [1 ]
Huang Nian-Yu [1 ]
机构
[1] China Three Gorges Univ, Coll Biol & Pharmaceut Sci, Hubei Key Lab Nat Prod Res & Dev, Yichang 443002, Peoples R China
基金
中国国家自然科学基金;
关键词
steroids; structural modification; N-hetercycles; antitumor; structure-activity; VITRO ANTIPROLIFERATIVE EVALUATION; IN-VITRO; ANTICANCER AGENTS; BIOLOGICAL EVALUATION; CHEMICAL-SYNTHESIS; CYTOTOXIC ACTIVITIES; E-SALIGNONE; DERIVATIVES; CANCER; RING;
D O I
10.14102/j.cnki.0254-5861.2011-1688
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Natural steroids have been showing notable cytotoxic activities, which are quite interesting lead compounds for the development of anticancer drug including estramustine and prednimustine. Considering that these semi-synthetic molecules are nitrogen mustard functionalized steroidal derivatives, the present review is focused on the methodologies of introducing nitrogen atom or nitrogen-containing heterocycles on A similar to D rings or side chains of steroids, and analysis of the structure-activity relationship (SAR) for these man-made cytotoxic steroids.
引用
收藏
页码:2007 / 2019
页数:13
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