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Bioorg Med Chem Lett ; 15(15): 3609-10, 2005 Aug 01.
Article in English | MEDLINE | ID: mdl-15967662

ABSTRACT

We have developed a concise synthesis of dielsiquinone 1, a potent cytotoxic agent related to anthraquinones. Electrochemical studies have shown that dielsiquinone is reduced to a semiquinone radical that does not react with O2 to generate toxic reactive oxygen species. These results strongly suggest that 1 should be less cardiotoxic than anthracyclines used in clinic and may therefore provide the basis for the development of safer anticancer drugs.


Subject(s)
Anthraquinones/chemical synthesis , Antibiotics, Antineoplastic/chemical synthesis , Aza Compounds/chemistry , Animals , Anthracyclines/pharmacology , Anthracyclines/toxicity , Anthraquinones/pharmacology , Antibiotics, Antineoplastic/pharmacology , Aza Compounds/chemical synthesis , Aza Compounds/pharmacology , Benzoquinones/chemistry , Oxygen/chemistry , Potentiometry/methods , Reactive Oxygen Species/chemistry , Reactive Oxygen Species/toxicity , Structure-Activity Relationship
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