Total synthesis and biological evaluation of fluorinated cryptophycins

被引:16
|
作者
Weiss, Christine [1 ]
Bogner, Tobias [1 ]
Sammet, Benedikt [1 ]
Sewald, Norbert [1 ]
机构
[1] Univ Bielefeld, Dept Chem, D-33501 Bielefeld, Germany
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2012年 / 8卷
关键词
antimitotic drug; cytotoxicity; depsipeptide; fluorinated natural product analogues; structure-activity relationship; POTENT CYTOTOXIC DEPSIPEPTIDE; EFFICIENT SYNTHESIS; ARENASTATIN-A; UNIT; PHARMACEUTICALS; PRECURSOR; LY355703;
D O I
10.3762/bjoc.8.231
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Cryptophycins are cytotoxic natural products that exhibit considerable activities even against multi-drug-resistant tumor cell lines. As fluorinated pharmaceuticals have become more and more important during the past decades, fluorine-functionalized cryptophycins were synthesized and evaluated in cell-based cytotoxicity assays. The unit A trifluoromethyl-modified cryptophycin proved to be highly active against KB-3-1 cells and exhibited an IC50 value in the low picomolar range. However, the replacement of the 3-chloro-4-methoxyphenyl-substituent in unit B by a pentafluorophenyl moiety resulted in a significant loss of activity.
引用
收藏
页码:2060 / 2066
页数:7
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