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天然二苯并氮杂卓 BU-4664L 及其衍生物的抗侵袭和抗血管生成活性。

Anti-invasive and anti-angiogenic activities of naturally occurring dibenzodiazepine BU-4664L and its derivatives.

机构信息

Biotechnology Research Center, Toyama Prefectural University, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan.

出版信息

Bioorg Med Chem Lett. 2010 Feb 1;20(3):963-5. doi: 10.1016/j.bmcl.2009.12.055. Epub 2009 Dec 21.

Abstract

In the screening for antitumor leads from microbial secondary metabolites, BU-4664L (1), a naturally occurring dibenzodiazepine, was found to inhibit tumor invasion and angiogenesis in vitro. Compound 1 inhibited the gelatinase activities of MMP-2 and MMP-9 and the cellular motility. Four derivatives (2-5) were synthesized from 1 and their antitumor activities were evaluated. Compounds 3 and 4 exhibited potent anti-angiogenic effects on HUVEC, together with remarkable inhibition of cell migration at nanomolar concentrations, and showed much lower cytotoxicity.

摘要

在微生物次级代谢产物的抗肿瘤先导化合物筛选中,发现天然存在的二苯并二氮杂卓 BU-4664L(1)能够在体外抑制肿瘤侵袭和血管生成。化合物 1 抑制 MMP-2 和 MMP-9 的明胶酶活性以及细胞迁移。从 1 合成了四个衍生物(2-5),并评估了它们的抗肿瘤活性。化合物 3 和 4 在纳摩尔浓度下对 HUVEC 具有很强的抗血管生成作用,同时显著抑制细胞迁移,且细胞毒性低得多。

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