Specific displacement of glutathione from the Pt(II)-glutathione adduct by Cu(II) in neutral phosphate buffer

doi:10.1016/S0162-0134(98)10043-0

淡江大學機構典藏 > 理學院 > 化學學系暨研究所 > 期刊論文 > Item 987654321/61725

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题名:	Specific displacement of glutathione from the Pt(II)-glutathione adduct by Cu(II) in neutral phosphate buffer
作者:	Cheng, Chien-chung;Pai, Chai-hsian
贡献者:	淡江大學化學學系
关键词:	Platinum-thiolate cleavage;Glutathione;S-bridged heterodinuclear;Regeneration
日期:	1998-01-01
上传时间:	2011-10-15 23:34:15 (UTC+8)
摘要:	The Pt–S bond of Pt(II)–glutathione (GS–Pt) complex was dissociable in neutral phosphate buffer at room temperature in the presence of Cu(II) ion. In addition, the chloro species, Pt(terpy)Cl+, was isolated and identified as the major cleavage product of Pt(terpy)(GS)2+ complex when CuCl2 was used. The Pt–S bond dissociation of Pt(terpy)(GS)2+ mediated by Cu(II) ion was shown to be a pH dependent process in the range of 4.5–8.0. At pH <7, NMR evidence was obtained for a S-bridged heterodinuclear unit formed between Pt(terpy)(GS)2+ and the Cu(II) ion; however, no Pt–S bond dissociation was observed up to 24 h. At pH ⩾ 7, NMR data suggested coordination of the amide nitrogen of GSH of Pt(terpy)(GS)2+ to the Cu(II) ion. We propose that the coordination of the amide nitrogen to the Cu(II) ion, together with the formation of the S-bridged heterodinuclear unit, induce the Pt–S bond dissociation in Pt(terpy)(GS)2+. These results may be exploited to develop a molecular activator to regenerate the anticancer activity in cisplatin pro-drugs.
關聯:	Journal of inorganic biochemistry 71(3-4), pp.109-113
DOI:	10.1016/S0162-0134(98)10043-0
显示于类别:	[化學學系暨研究所] 期刊論文

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