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J Am Chem Soc. 2016 Dec 7;138(48):15559-15562. Epub 2016 Nov 28.

Mechanism of Nucleophilic Activation of (-)-Lomaiviticin A.

Author information

1
Department of Chemistry, Yale University , New Haven, Connecticut 06520, United States.
2
Department of Pharmacology, Yale School of Medicine , New Haven, Connecticut 06520, United States.

Abstract

(-)-Lomaiviticin A (1) is a C2-symmetric cytotoxin that contains two diazofluorene functional groups and which induces double-strand breaks (DSBs) in DNA. Evidence suggests DNA cleavage is initiated by hydrogen atom abstraction from the deoxyribose backbone. Here we demonstrate the formation of the vinyl radicals 1· and 2· from 1 by 1,7-addition of thiols to the diazofluorenes. These radicals can affect hydrogen atom abstraction from methanol and acetone. The first addition of thiol to 1 proceeds at a much greater rate than the second. The diazosulfide 5 formed en route to 1· has been detected at -50 °C and undergoes decomposition to 1· with a half-life of 110 min at -20 °C under air. These data, which constitute the first direct evidence for the generation of 1· and 2· from 1, provide insights into the mechanism of DNA cleavage by 1.

PMID:
27934014
PMCID:
PMC5339879
DOI:
10.1021/jacs.6b09657
[Indexed for MEDLINE]
Free PMC Article

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