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新型组蛋白甲基转移酶 SET7/9 的双底物型抑制剂的开发。

Development of novel bisubstrate-type inhibitors of histone methyltransferase SET7/9.

机构信息

Tokyo Medical and Dental University, Chiyoda-ku, Japan.

出版信息

Bioorg Med Chem. 2010 Dec 1;18(23):8158-66. doi: 10.1016/j.bmc.2010.10.022. Epub 2010 Oct 14.

Abstract

Histone modification, for example, by histone deacetylase (HDAC) and histone lysine methyltransferase (HMT), plays an important role in regulating gene expression. To obtain novel inhibitors as tools for investigating the physiological function of members of the HMT family, we designed and synthesized novel inhibitors, which are amine analogues of adenosylmethionine (AdoMet; the cofactor utilized in the methylation reaction) bearing various alkylamino groups coupled via an ethylene linker. The inhibitory activities of these compounds towards SET7/9, an HMT, were evaluated. It was found that introduction of an alkylamino group increased the inhibitory activity.

摘要

组蛋白修饰,例如组蛋白去乙酰化酶 (HDAC) 和组蛋白赖氨酸甲基转移酶 (HMT),在调节基因表达方面发挥着重要作用。为了获得新型抑制剂作为研究 HMT 家族成员生理功能的工具,我们设计并合成了新型抑制剂,这些抑制剂是腺苷甲硫氨酸 (AdoMet;甲基化反应中使用的辅因子) 的胺类似物,通过乙烯连接子偶联各种烷基氨基。评估了这些化合物对 SET7/9(一种 HMT)的抑制活性。结果发现,引入烷基氨基会增加抑制活性。

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