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Design, Synthesis and biological evaluation of novel acridine-polyamine conjugates against prostate cancer

Maurice, HB, Phillips, Roger and Karodia, N (2009) Design, Synthesis and biological evaluation of novel acridine-polyamine conjugates against prostate cancer. African Journal of Pharmacy and Pharmacology, 3 (12). pp. 602-610. ISSN ISSN 1996-0816

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Abstract

Prostate cancer is the most common cause of cancer death in men, aged 85 and over. Androgen receptor, a single polypeptide with three functional domains is very important during initiation and progression of the disease. In this study, a DNA intercalating agent, acridine is linked to the testosterone via a polyamine linker to obtain a compound with trifunctional characteristics, where the acridine intercalates the DNA, the polyamine linker binds the phosphoryl groups of the DNA backbone and the testosterone moiety binds into the AR ligand binding domain, with which its DNA binding domain is bound already to the DNA. This trifunctional compound and related derivatives have been synthesized and tested against androgen dependent- and androgen independent- prostate cancer cell lines and they have demonstrated to be cytotoxic at the micromolar concentrations.

Item Type: Article
Subjects: R Medicine > RM Therapeutics. Pharmacology
Schools: School of Applied Sciences
Related URLs:
Depositing User: Roger Phillips
Date Deposited: 26 Feb 2015 16:37
Last Modified: 30 Nov 2016 17:57
URI: http://eprints.hud.ac.uk/id/eprint/23475

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