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HIF-1α 抑制剂:新型麦角甾醇 O 和 P 类似物的合成与生物学评价。

HIF-1α inhibitors: synthesis and biological evaluation of novel moracin O and P analogues.

机构信息

College of Pharmacy, Dongguk University-Seoul, Seoul 100-715, South Korea.

出版信息

Eur J Med Chem. 2011 Jun;46(6):2386-96. doi: 10.1016/j.ejmech.2011.03.022. Epub 2011 Mar 21.

Abstract

The natural products moracins O and P exhibited potent in vitro inhibitory activity against hypoxia-inducible factor (HIF-1), which is a key mediator during adaptation of cancer cells to tumour hypoxia. Systematic variations of the structures of benzofuran type moracins were made and structure-activity relationship analysis showed the importance of the 2-arylbenzofuran ring and the (R)-configuration of the core scaffold. Further evaluation of the representative compound 5 showed its inhibitory effect on HIF-1α protein accumulation and target gene expression under hypoxia.

摘要

天然产物莫拉辛 O 和 P 对缺氧诱导因子 (HIF-1) 表现出强烈的体外抑制活性,HIF-1 是癌细胞适应肿瘤缺氧的关键介质。对苯并呋喃型莫拉辛的结构进行了系统的变化,结构-活性关系分析表明 2-芳基苯并呋喃环和核心支架的 (R)-构型的重要性。对代表性化合物 5 的进一步评估表明,它在缺氧条件下抑制 HIF-1α 蛋白积累和靶基因表达。

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