Control of the cytotoxicity of dansylated polytheonamide mimic, an artificial peptide ion channel, by modification of the N-terminal structure

被引:4
作者
Itoh, Hiroaki [1 ]
Matsutaka, Shoko [1 ]
Kuranaga, Takefumi [1 ]
Inoue, Masayuki [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
基金
日本学术振兴会;
关键词
Cytotoxic agents; Natural products; Structure-activity relationships; Peptides; PERFORMANCE LIQUID-CHROMATOGRAPHY; MARINE SPONGE; FUNCTIONAL-ANALYSIS; GRADIENT ELUTION; POTENT CYTOTOXIN; THIOESTER METHOD; B DISCOVERY; LIPOPHILICITY; POLYPEPTIDES; PERMUTATION;
D O I
10.1016/j.tetlet.2013.12.007
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We demonstrate that the cytotoxicity of dansylated polytheonamide mimic (2) is controlled by chemical modification of its N-terminal structure. Dansylated polytheonamide mimic (2) is an ion channel peptide which displays potent cytotoxicity against P388 mouse leukemia cells (IC50 = 12 nM). To modulate its cytotoxicity, three analogues of 2, possessing distinct N-terminal structures with different hydrophobicities, were synthesized and their cytotoxicities were evaluated. This focused structure-activity relationship study unveiled that the cytotoxicity of 2 is enhanced 10-fold by simply changing its N-terminal 5,5-dimethyl-2-oxohexanamide to the more hydrophobic palmitamide. The data obtained here provide new understanding for the functional control of the artificial ion channel peptide 2. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:728 / 731
页数:4
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