Cytotoxic ring A-modified steroid analogues derived from Grundmann's ketone

被引:21
|
作者
Mayer, Christoph D. [1 ]
Bracher, Franz [1 ]
机构
[1] Univ Munich, Dept Pharm, Zentrum Pharmaforsch, D-81377 Munich, Germany
关键词
Steroid analogues; Cycloaddition; Cytotoxic activity; WITHANOLIDES; INHIBITORS; OXIDATION; ASSAY; NCI;
D O I
10.1016/j.ejmech.2011.04.036
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of steroid and azasteroid analogues containing a six-membered ring A with various functionalities were synthesized. Furthermore, the syntheses of tetracyclic analogues bearing a five-membered A-ring and the syntheses of a number of bicyclic secosteroid analogues were carried out. All compounds were tested for their antibacterial, antifungal and cytotoxic activities. Among all tested compounds 7 and 9 showed outstanding cytotoxic activities but were devoid of antimicrobial activities. The cytotoxic activities of compounds 7, 9 and 10 were initially verified by the National Cancer Institute (NCI) in a one-dose 60 cell assay. In accordance with our results 7 and 9 satisfied pre-determined threshold inhibition criteria for progression to the 5-dose NCI screening, which revealed a selective activity profile for both candidates. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:3227 / 3236
页数:10
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