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

Ho, A, Kim, YE, Lee, HS et al. (2006). SAR studies of 2-methoxyestradiol and development of its analogs as probes of anti-tumor mechanisms . Bioorganic and Medicinal Chemistry Letters, 16(13), 3383-3387. 10.1016/j.bmcl.2006.04.030

cited authors

  • Ho, A; Kim, YE; Lee, HS; Cyrus, K; Baek, SH; Kim, KB

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. © 2006 Elsevier Ltd. All rights reserved.

authors

publication date

  • July 1, 2006

published in

Digital Object Identifier (DOI)

start page

  • 3383

end page

  • 3387

volume

  • 16

issue

  • 13