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    The reduction of anti-tumour diaziridinyl benzoquinones.

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    Authors
    Butler, John
    Hoey, Brigid M
    Lea, J S
    Affiliation
    Department of Biophysical Chemistry, Paterson Institute for Cancer Research, Christie Hospital and Holt Radium Institute, Manchester, M20 9BX, U.K.
    Issue Date
    1987-08-13
    
    Metadata
    Show full item record
    Abstract
    The properties of the semiquinone radicals produced for 2,5-bis(carboethoxyamino)-3,6-diaziridinyl-1,4-benzoquinone (AZQ) and 2,5-bis(2-hydroxyethylamino)-3,6-diaziridinyl-1,4-benzoquinone (BZQ), have been investigated. AZQ semiquinone radicals can be produced from the reduction of AZQ by superoxide radicals, whereas BZQ semiquinone radicals are unstable in the presence of oxygen. The one-electron reduction potentials of the couples Q/Q-. at pH 7.0 were determined as -70 +/- 10 mV for AZQ and -376 +/- 15 mV for BZQ. The difference in these potentials is explained. As a consequence of ESR studies on the enzymatically produced radicals, we have considered the factors which determine the detection of ESR signals for reduced quinones produced in a biological system.
    Citation
    The reduction of anti-tumour diaziridinyl benzoquinones. 1987, 925 (2):144-9 Biochim Biophys Acta
    Journal
    Biochimica et Biophysica Acta
    URI
    http://hdl.handle.net/10541/114969
    DOI
    10.1016/0304-4165(87)90103-6
    PubMed ID
    3040109
    Type
    Article
    Language
    en
    ISSN
    0006-3002
    ae974a485f413a2113503eed53cd6c53
    10.1016/0304-4165(87)90103-6
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

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