Kinamycin-mediated DNA cleavage under biomimetic conditions |
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Authors: | T. Eric Ballard |
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Affiliation: | Department of Chemistry, North Carolina State University, Raleigh, NC 27695-8204, United States |
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Abstract: | The kinamycins are biologically active secondary metabolites characterized by an uncommon diazobenzo[b]fluorene skeleton. Kinamycin D has been shown to potently cleave DNA under mild biomimetic conditions. Use of the endogenously abundant reductant glutathione at 570 μM, kinamycin D effectively cleaved DNA in a concentration, temperature, and time-dependent fashion. Dithiothreitol also proved effective at low concentration while other reductants failed to induce DNA cleavage. Mechanistic consequences of the DNA cleavage results are described. |
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