Casely-Hayford, M. A., Pors, K., Patterson, L. H., Gerner, C., Neidle, S. and Searcey, M. ORCID: https://orcid.org/0000-0003-2273-8949 (2005) Truncated azinomycin analogues intercalate into DNA. Bioorganic & Medicinal Chemistry Letters, 15 (3). pp. 653-656. ISSN 0960-894X
Full text not available from this repository.Abstract
The design and synthesis of a potentially more therapeutically-viable azinomycin analogue 4 based upon 3 has been completed. It involved coupling of a piperidine mustard to the acid chloride of the azinomycin chromophore. Both the designed azinomycin analogue 4 and the natural product 3 bind to DNA and cause unwinding, supporting an intercalative mode of binding. (C) 2004 Elsevier Ltd. All rights reserved.
Item Type: | Article |
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Faculty \ School: | Faculty of Science > School of Pharmacy (former - to 2024) |
UEA Research Groups: | Faculty of Science > Research Groups > Medicinal Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemical Biology and Medicinal Chemistry (former - to 2021) |
Depositing User: | Rachel Smith |
Date Deposited: | 13 Jun 2011 13:35 |
Last Modified: | 24 Sep 2024 09:56 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/32137 |
DOI: | 10.1016/j.bmcl.2004.11.037 |
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