Novel antileukemic agents derived from tamibarotene and nitric oxide donors

被引:13
|
作者
Bian, Haiyong [1 ]
Feng, Jinhong [1 ]
Li, Minyong [1 ]
Xu, Wenfang [1 ]
机构
[1] Shandong Univ, Dept Med Chem, Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China
关键词
Multi-target drugs; Nitric oxide; RAR agonist; Synthesis; Biological evaluation; FUROXANS; DERIVATIVES; RELEASE;
D O I
10.1016/j.bmcl.2011.09.103
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel nitric oxide-releasing tamibarotene derivatives were synthesized by coupling nitric oxide (NO) donors with tamibarotene via various spacers, and were evaluated for their antiproliferative activities against human leukemic HL-60, NB4 and K562 cell lines in vitro. The test results showed that three compounds (7g, 9a and 9e) exhibited more potent antileukemic activity than the control tamibarotene. Furthermore, the preliminary structure-activity analysis revealed that amino acids serving as spacers could bring about significantly improved biological activities of NO donor hybrids. These interesting results could provide new insights into the development of NO-based antileukemic agents. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7025 / 7029
页数:5
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