Amide bond direction modulates G-quadruplex recognition and telomerase inhibition by 2,6 and 2,7 bis-substituted anthracenedione derivatives.

Zagotto, G., Sissi, C., Moro, S., Del Ben, D., Parkinson, G.N., Fox, S., Neidle, S. and Palumbo, M. (2008) Amide bond direction modulates G-quadruplex recognition and telomerase inhibition by 2,6 and 2,7 bis-substituted anthracenedione derivatives. Bioorganic & Medicinal Chemistry, 16 (1). pp. 354-361. 10.1016/j.bmc.2007.09.040.

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DOI: 10.1016/j.bmc.2007.09.040


Item Type:Article
Additional Information:Full text available electronically from the School of Pharmacy Library.
Departments, units and centres:Department of Pharmaceutical and Biological Chemistry > Cancer Research UK Biomolecular Structure Group
ID Code:1188
Journal or Publication Title:Bioorganic & Medicinal Chemistry
Deposited By:Library Staff
Deposited On:28 Apr 2009 16:44
Last Modified:04 Feb 2011 16:33

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