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dc.contributor.authorCasely-Hayford, M.A.*
dc.contributor.authorPors, Klaus*
dc.contributor.authorPatterson, Laurence H.*
dc.contributor.authorGerner, C.*
dc.contributor.authorNeidle, S.*
dc.contributor.authorSearcey, M.*
dc.date.accessioned2009-11-16T07:49:49Z
dc.date.available2009-11-16T07:49:49Z
dc.date.issued2005
dc.identifier.citationCasely-Hayward, M., Pors, K., Patterson, L.H. and Gerner, C. et al. (2005). Truncated azinomycin analogues intercalate into DNA. Bioorganic Medicinal Chemistry Letters. Vol. 15, No. 3, pp. 653-656.
dc.identifier.urihttp://hdl.handle.net/10454/3908
dc.descriptionNo
dc.description.abstractThe 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. Graphical abstract A designed analogue of the left half of azinomycin has been synthesized and unwinds supercoiled DNA.
dc.language.isoen
dc.subjectAzinomycin
dc.subjectIntercalation
dc.subjectDNA unwinding
dc.subjectSynthesis
dc.subjectAnalogues
dc.titleTruncated azinomycin analogues intercalate into DNA.
dc.status.refereedYes
dc.typeArticle
dc.type.versionNo full-text in the repository
dc.identifier.doihttps://doi.org/10.1016/j.bmcl.2004.11.037
dc.openaccess.statusclosedAccess


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