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- W2060391323 endingPage "541" @default.
- W2060391323 startingPage "529" @default.
- W2060391323 abstract "The selective oestrogen receptor modulator tamoxifen is a leading agent in the adjuvant treatment of breast cancer. Several organometallic moieties have been vectorised with tamoxifen, in order to improve on the latter's antiproliferative properties by the addition of a potentially cytotoxic moiety, and have been evaluated versus both oestrogen receptor positive (MCF7) and oestrogen receptor negative (MDA-MB231) breast cancer cells. For tamoxifen analogues with ((R,R)-trans-1,2-diaminocyclohexane)platinum(II), cyclopentadienyl rhenium tricarbonyl, and ruthenocene tethers, there was no enhancement of the antiproliferative effect on oestrogen receptor positive cells, nor any cytotoxic effect on oestrogen receptor negative cells, while those containing cyclopentadienyl titanium dichloride showed an oestrogenic effect. However, compounds where ferrocene replaces tamoxifen's phenyl ring were strongly cytotoxic against both cell lines. The synthesis and biological results of these compounds is reviewed and placed in the historic context of inorganic compounds in therapy." @default.
- W2060391323 created "2016-06-24" @default.
- W2060391323 creator A5010766834 @default.
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- W2060391323 creator A5053559316 @default.
- W2060391323 creator A5073957893 @default.
- W2060391323 creator A5074662671 @default.
- W2060391323 date "2006-01-01" @default.
- W2060391323 modified "2023-10-16" @default.
- W2060391323 title "Metal complex SERMs (selective oestrogen receptor modulators). The influence of different metal units on breast cancer cell antiproliferative effects" @default.
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