首页> 外文OA文献 >A Study of the Antitumour Activity of Four Triorganophosphinegold(I) Thiolates: R3 PAu(SR′), R = Ph, Cy, Et; SR′H = 6-Mercaptopurine and R = Et; SR′H = 6-Thioguanine
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A Study of the Antitumour Activity of Four Triorganophosphinegold(I) Thiolates: R3 PAu(SR′), R = Ph, Cy, Et; SR′H = 6-Mercaptopurine and R = Et; SR′H = 6-Thioguanine

机译:四种抗肿瘤活性的研究 三有机膦金(I)硫醇盐:R3 PAu(SR'),R = Ph,Cy,Et; SR'H = 6-巯基嘌呤 和R = Et; SR'H = 6-硫鸟嘌呤

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摘要

The antitumour activities of four triorganophosphinegold(I) thiolates, R2PAu(S′R) [R = Ph, Cy, Et; SR′H = 6-mercaptopurine and R Et; SR′H = 6-thioguanine] against the National Cancer Institute (NCI) panel of 60 cell lines are reported The [Cy3PAu(6-MP)] complex proved to be the more cytotoxic of the four complexes tested. For the 6-MP series, an order of cytotoxicity was established such that the activity followed the order R = Cy > Ph > Et. Sub-panel selectivity against the Leukemia cell lines was found for each of [Cy3 PAu(6-MP)] and [Et3PAu(6-TG)].
机译:四种三有机膦金(I)硫醇盐R2PAu(S'R)的抗肿瘤活性[R = Ph,Cy,Et; SR'H = 6-巯基嘌呤,R Et;据报道,针对国家癌症研究所(NCI)的60个细胞系,SR'H = 6-硫代鸟嘌呤] [Cy3PAu(6-MP)]复合物在所测试的四种复合物中被证明具有更高的细胞毒性。对于6-MP系列,确定了细胞毒性的顺序,以使活性遵循以下顺序:R = Cy> Ph> Et。对于[Cy3 PAu(6-MP)]和[Et3PAu(6-TG)]均发现了针对白血病细胞系的亚面板选择性。

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