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    Synthesis and anticancer activities of 4-oxobenzopyrano[2,3-d]pyrimidines.

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    Authors
    Hadfield, John A
    Pavlidis, V H
    Perry, P J
    McGown, Alan T
    Affiliation
    Cancer Research Campaign Section of Drug Development and Imaging, Paterson Institute for Cancer Research, Manchester, UK. jhadfield@picr.man.ac.uk
    Issue Date
    1999-07
    
    Metadata
    Show full item record
    Abstract
    Several 2-aryl-4-oxoxbenzopyrano[2,3-d]pyrimidines have previously been shown to exhibit in vivo antitumor activity in mice with P388 lymphocytic leukemia. In the present study, a series of novel substituted benzopyrano[2,3-d]pyrimidines have been prepared and tested for cytotoxic activity against a panel of cancer cell lines including the P388 lymphocytic leukemia cell line. The unsubstituted parent compound, some methoxylated derivatives and a cyclohexyl derivative all exhibited potent cytotoxic activity (IC50 values 0.3-0.64 microM). A number of derivatives, including the unsubstituted parent pyrimidine, were shown to cause a significant perturbation in cell cycle kinetics with an observed 2- to 3-fold increase in cells in the G2/M phase of the cell cycle. Furthermore, a polymethoxylated derivative, 2-(3,4,5-trimethoxyphenyl)-9-methoxy-4-oxo-2,3-dihydrobenzopyrano[ 2,3-d]pyrimidine 13, was shown to be selectively active against a number of human ovarian cell lines.
    Citation
    Synthesis and anticancer activities of 4-oxobenzopyrano[2,3-d]pyrimidines. 1999, 10 (6):591-5 Anticancer Drugs
    Journal
    Anti-Cancer Drugs
    URI
    http://hdl.handle.net/10541/91373
    PubMed ID
    10885907
    Type
    Article
    Language
    en
    ISSN
    0959-4973
    Collections
    All Paterson Institute for Cancer Research

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