| Literature DB >> 25909279 |
Daniel E Beck1, Monica Abdelmalak2, Wei Lv1, P V Narasimha Reddy1, Gabrielle S Tender2, Elizaveta O'Neill1, Keli Agama2, Christophe Marchand2, Yves Pommier2, Mark Cushman1.
Abstract
3-Nitroindenoisoquinoline human topoisomerase IB (Top1) poisons have potent antiproliferative effects on cancer cells. The undesirable nitro toxicophore could hypothetically be replaced by other functional groups that would retain the desired biological activities and minimize potential safety risks. Eleven series of indenoisoquinolines bearing 3-nitro bioisosteres were synthesized. The molecules were evaluated in the Top1-mediated DNA cleavage assay and in the National Cancer Institute's 60 cell line cytotoxicity assay. The data reveal that fluorine and chlorine may substitute for the 3-nitro group with minimal loss of Top1 poisoning activity. The new information gained from these efforts can be used to design novel indenoisoquinolines with improved safety.Entities:
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Year: 2015 PMID: 25909279 PMCID: PMC7753975 DOI: 10.1021/acs.jmedchem.5b00303
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446