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2-甲氧基雌二醇的构效关系研究及其类似物作为抗肿瘤机制探针的开发。

SAR studies of 2-methoxyestradiol and development of its analogs as probes of anti-tumor mechanisms.

作者信息

Ho Abby, Kim Yang-eon, Lee Hyosung, Cyrus Kedra, Baek Sun-Hee, Kim Kyung-Bo

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, USA.

出版信息

Bioorg Med Chem Lett. 2006 Jul 1;16(13):3383-7. doi: 10.1016/j.bmcl.2006.04.030. Epub 2006 May 2.

Abstract

The major estrogen metabolite 2-methoxyestradiol (2ME) has been shown to target tumor cells without severe side effects and is currently being evaluated in clinical trials for several types of cancer. Despite its promise for use in clinical setting, the mechanism(s) by which 2ME exerts its anti-tumor activity is not clearly defined at this time. Employing organic chemistry tools, we synthesized 2ME analogs with which 2ME affinity column was prepared, enabling us to detect a protein that selectively interacts with 2ME. This 2ME analog will be useful as a probe to identify the biological target(s) of 2ME and study their functions in tumor cells.

摘要

主要雌激素代谢物2-甲氧基雌二醇(2ME)已被证明可靶向肿瘤细胞且无严重副作用,目前正在针对几种癌症进行临床试验评估。尽管其在临床应用中有前景,但目前2ME发挥抗肿瘤活性的机制尚不清楚。利用有机化学工具,我们合成了2ME类似物,并制备了2ME亲和柱,使我们能够检测到一种与2ME选择性相互作用的蛋白质。这种2ME类似物将作为一种探针,用于鉴定2ME的生物学靶点并研究它们在肿瘤细胞中的功能。

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