Show simple item record

dc.contributor.authorHargreaves, Robert H J
dc.contributor.authorHartley, John A
dc.contributor.authorButler, John
dc.date.accessioned2009-12-29T10:41:07Z
dc.date.available2009-12-29T10:41:07Z
dc.date.issued2000-11-01
dc.identifier.citationMechanisms of action of quinone-containing alkylating agents: DNA alkylation by aziridinylquinones. 2000, 5:E172-80 Front. Biosci.en
dc.identifier.issn1093-4715
dc.identifier.pmid11056081
dc.identifier.urihttp://hdl.handle.net/10541/88618
dc.description.abstractAziridinyl quinones can be activated by cellular reductases eg. DT-diaphorase and cytochrome P450 reductase to form highly reactive DNA alkylating agents. The mechanisms by which this activation and alkylation take place are many and varied. Using clinically relevant and experimental agents this review will describe many of these mechanisms. The agents discussed are Mitomycin C, EO9 and analogues, diaziridinylbenzoquinones and the pyrrolo[1, 2-alpha]benzimidazolequinones.
dc.language.isoenen
dc.subject.meshAlkylation
dc.subject.meshAntineoplastic Agents, Alkylating
dc.subject.meshAziridines
dc.subject.meshBenzimidazoles
dc.subject.meshBenzoquinones
dc.subject.meshCarbazilquinone
dc.subject.meshDNA
dc.subject.meshDoxorubicin
dc.subject.meshHumans
dc.subject.meshIndolequinones
dc.subject.meshIndoles
dc.subject.meshMitomycin
dc.subject.meshMolecular Structure
dc.subject.meshOxidation-Reduction
dc.subject.meshQuinones
dc.subject.meshStructure-Activity Relationship
dc.titleMechanisms of action of quinone-containing alkylating agents: DNA alkylation by aziridinylquinones.en
dc.typeArticleen
dc.contributor.departmentCRC Drug Development Group, Paterson Institute for Cancer Research, Wilmslow Road, Manchester, M20 4BX, U.K.en
dc.identifier.journalFrontiers in Bioscienceen
html.description.abstractAziridinyl quinones can be activated by cellular reductases eg. DT-diaphorase and cytochrome P450 reductase to form highly reactive DNA alkylating agents. The mechanisms by which this activation and alkylation take place are many and varied. Using clinically relevant and experimental agents this review will describe many of these mechanisms. The agents discussed are Mitomycin C, EO9 and analogues, diaziridinylbenzoquinones and the pyrrolo[1, 2-alpha]benzimidazolequinones.


This item appears in the following Collection(s)

Show simple item record