| Literature DB >> 27890379 |
Brandon A Carter-Cooper1, Steven Fletcher2, Dana Ferraris3, Eun Yong Choi1, Dahlia Kronfli1, Smaraki Dash1, Phuc Truong3, Edward A Sausville1, Rena G Lapidus1, Ashkan Emadi4.
Abstract
The synthesis, characterization and antileukemic activity of rationally designed amino dimeric naphthoquinone (BiQ) possessing aziridine as alkylating moiety is described. Bis-aziridinyl BiQ decreased proliferation of acute myeloid leukemia (AML) cell lines and primary cells from patients, and exhibited potent (nanomolar) inhibition of colony formation and overall cell survival in AML cells. Effective production of reactive oxygen species (ROS) and double stranded DNA breaks (DSB) induced by bis-aziridinyl BiQ is reported. Bis-dimethylamine BiQ, as the isostere of bis-aziridinyl BiQ but without the alkylating moiety did not show as potent anti-AML activity. Systemic administration of bis-aziridinyl BiQ was well tolerated in NSG mice. Copyright ÂEntities:
Keywords: Acute myeloid leukemia; Aziridine; DNA damage; Naphthoquinone; Reactive oxygen species
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Year: 2016 PMID: 27890379 PMCID: PMC5654471 DOI: 10.1016/j.bmcl.2016.11.045
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823