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Allosteric, chiral-selective drug binding to DNA

The binding interactions of (−)-daunorubicin (WP900), a newly synthesized enantiomer of the anticancer drug (+)-daunorubicin, with right- and left-handed DNA, have been studied quantitatively by equilibrium dialysis, fluorescence spectroscopy, and circular dichroism. (+)-Daunorubicin binds selective...

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Autors principals: Qu, Xiaogang, Trent, John O., Fokt, Izabela, Priebe, Waldemar, Chaires, Jonathan B.
Format: Artigo
Idioma:Inglês
Publicat: The National Academy of Sciences 2000
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC17289/
https://ncbi.nlm.nih.gov/pubmed/11027298
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