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Bioorganic & Medicinal Chemistry Letters
Volume 17, Issue 9, 1 May 2007, Pages 2421-2424
 
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doi:10.1016/j.bmcl.2007.02.037    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2007 Elsevier Ltd All rights reserved.

Synthesis of the new pseudo-symmetrical tamoxifen derivatives and their anti-tumor activity

Isamu Shiinaa, Corresponding Author Contact Information, E-mail The Corresponding Author, Yoshiyuki Sanoa, Kenya Nakataa, Takaaki Kikuchia, Akane Sasakia, Masahiko Ikekitab, Corresponding Author Contact Information, E-mail The Corresponding Author and Yoshimune Hasomeb

aDepartment of Applied Chemistry, Faculty of Science, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan bDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Yamazaki, Noda, Chiba 278-8510, Japan

Received 2 November 2006; 
revised 13 February 2007; 
accepted 15 February 2007. 
Available online 17 February 2007.

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Abstract

Three new pseudo-symmetrical tamoxifen derivatives, RID-B (15), C (16), and D (17), were synthesized via the novel three-component coupling reaction, and the structure–activity relationships of the pseudo-symmetrical tamoxifen derivatives were examined. It was discovered that 15 strongly inhibits the viability of HL-60 human acute promyelocytic leukemia, whereas 16 possesses medium activity against the cell line and 17 has no effect on the cell viability. The agarose gel electrophoresis for DNA cleavage showed the cell death might be induced by apoptosis.

Graphical abstract

The synthesis of new tamoxifen derivatives is reported. Their effects on growth of HL-60 cells are determined.


Keywords: Tamoxifen; SERMs; Selective estrogen receptor modulators; pseudo-Symmetrical structure; Anti-tumor activity; Apoptosis; Synthesis

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