Novel adducts of the anticancer drug oxaliplatin with glutathione and redox reactions with glutathione disulfide

被引:61
作者
Fakih, S [1 ]
Munk, VP [1 ]
Shipman, MA [1 ]
Murdoch, PD [1 ]
Parkinson, JA [1 ]
Sadler, PJ [1 ]
机构
[1] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
关键词
antitumour agents; platinum; S ligands; peptides; redox chemistry;
D O I
10.1002/ejic.200390156
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reactions of [Pt(rac-1,2-DACH)Cl-2], [Pt(1R,2R-DACH)Cl-2] and the anticancer drug oxaliplatin with the tripeptide glutathione and glutathione disulfide have been studied by HPLC, ESI-MS and NMR methods. The same two major products are formed in each reaction: a thiolate-bridged dimer and a novel thiolate-bridged dinuclear macrochelate containing a nine-membered chelate ring. Redox reactions of Pt-II anticancer drugs with biological disulfides are of potential importance to their mechanism of action. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
引用
收藏
页码:1206 / 1214
页数:9
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