摘要:
Several novel thiocarbohydrate phosphinogold(I) complexes were prepared via the reaction of n-gluconamidoalkyl thiol (Ll-L7) (where L1 -L4 = n-gluconamidoalkyl thiol (n = 1-4), L5 L7 = acetylated n-gluconamidoalkyl thiol (n = 1-3)) with the gold precursors [AuCl(PPh3)], [Au2Cl2(dppe)], [Au2Cl2(dPPP)] and [Au2Cl2(dppb)], leading to the new gold(I) complexes [Au(L1) (PPh3)] (1-4), [Au(L5)(PPh3)] (5-7), IAu2(L1)(2)(dPPe)1 (8-11), (Au-2(L5)(2)(dPPx)1 (L2-14), [(Au-2(L6)(2)) (dppx)] (15-17), [Au-2(L7)(2)(dPPx)] (18-20), {where dppe= 1,2-bis(diphenylphosphino)ethane (x = e), dppp = 1,3-bis(diphenylphosphino)propane (x = p) and dppb = 1,4-bis-(diphenylphosphino)butane (x = b)). These gold complexes were characterized by a combination of NMR and infrared spectroscopy, microanalysis and mass spectrometry. Complexes 8,12,14-16 (IC50 values between 0.003 and 1.8 p.M) are all active against MCF7, HCT116 and PO cells. Complex 8 recorded the highest IC50 value of 0.003 mu M against PO. Complex 14 was found to be selective towards both MCF7 and PC3 cells with a TS value of 142.1, while compounds 15 and 16 were highly selective toward PO cells with TS values of 970.0 and 937.5, respectively. (C) 2017 Elsevier Ltd. All rights reserved.