Design, synthesis, and antihepatocellular carcinoma activity of nitric oxide releasing derivatives of oleanolic acid.

Design, synthesis, and antihepatocellular carcinoma activity of nitric oxide releasing derivatives of oleanolic acid.
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DOI:
10.1021/jm800167u
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发表时间:
2008-08-14
影响因子:
7.3
通讯作者:
Tian J
Tian J
中科院分区:
医学1区
文献类型:
--
作者:
Chen L;Zhang Y;Kong X;Lan E;Huang Z;Peng S;Kaufman DL;Tian J

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合成了一种新型的呋咱基一氧化氮(NO)释放型油酸衍生物,用于肝癌的潜在治疗。六个化合物在人肝细胞癌(HCC)细胞中产生高水平的NO,并在体外对HCC表现出较强的细胞毒性。用8b或16 b处理显著抑制体内HCC肿瘤的生长。这些数据提供了一个原则上的证据,氧化呋咱/OA杂合物可用于人类肝癌的治疗干预。
Novel furoxan-based nitric oxide (NO) releasing derivatives of oleanolic acid (OA) were synthesized for potential therapy of liver cancers. Six compounds produced high levels of NO in human hepatocellular carcinoma (HCC) cells and exhibited strong cytotoxicity selectively against HCC in vitro. Treatment with 8b or 16b significantly inhibited the growth of HCC tumors in vivo. These data provide a proof-in-principle that furoxan/OA hybrids may be used for therapeutic intervention of human liver cancers.
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