Anti-tumor activity, in vitro and in vivo, of some triphenylphosphinegold(I) thionucleobases

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Abstract

The [Ph3PAu(6-MP)] complex, where 6-MPH is 6-mercaptopurine, is active against the cisplatin-resistant cell line, mouse leukaemia L1210/DDP, as is the precursor compound [Ph3PAuCl], suggesting that the thiolate is not critical for activity. Against the human cell lines, FaDu (squamous cell carcinoma) and SKOV-3 (ovarian carcinoma), both [Ph3PAu(6-MP)] and [Ph3PAu(6-TG)], where 6-TGH is 6-thioguanine, were active. [Ph3PAu(6-MP)] was active against a murine PC6 plasmacytoma, but not as active as cisplatin.

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Webster, L. K., Rainone, S., Horn, E., & Tiekink, E. R. T. (1996). Anti-tumor activity, in vitro and in vivo, of some triphenylphosphinegold(I) thionucleobases. Metal-Based Drugs, 3(2), 63–66. https://doi.org/10.1155/MBD.1996.63

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