Modifying the properties of platinum(IV) complexes in order to increase biological effectiveness

被引:86
作者
Hambley, TW [1 ]
Battle, AR
Deacon, GB
Lawrenz, ET
Fallon, GD
Gatehouse, BM
Webster, LK
Rainone, S
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Monash Univ, Dept Chem, Clayton, Vic 3168, Australia
[3] Peter MacCallum Canc Inst, Pharmacol & Dev Therapeut Unit, Melbourne, Vic 8006, Australia
基金
澳大利亚研究理事会;
关键词
platinum(IV); complexes;
D O I
10.1016/S0162-0134(99)00133-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The preparation of a series of novel Pt(IV) complexes containing the anionic polyfluoroaryl ligands, 2,3,5,6-tetrafluorophenyl (p-HC6F4), 2,3,5,6-tetrafluoro-4-methoxyphenyl (p-MeOC6F4) and pentafluorophenyl (C6F5) are described. The crystal structure of a representative complex, [Pt(p-MeOC6F4)(2)(O2CEt)(2)(en)] (en = ethane-1,2-diamine) was determined and confirms the trans arrangement of the carboxylato ligands. Reduction potentials of the series of complexes reveal that replacement of equatorial chloro ligands by polyfluoroaryl ligands makes reduction substantially more difficult. They also confirm previously reported trends in that complexes having axial carboxylato ligands are more readily reduced than those having axial hydroxo ligands. Reduction potentials and in vitro activities showed no obvious correlations. Moderate to high activity was observed for many complexes in the series, including some of those that were very difficult to reduce. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:3 / 12
页数:10
相关论文
共 37 条
[1]  
Abrams M.J., 1989, [No title captured], Patent No. [EP 328274, 328274]
[2]  
BRAMWELL VHC, 1985, CANCER TREAT REP, V69, P409
[3]   SYNTHESIS, CHARACTERIZATION, AND PROPERTIES OF A GROUP OF PLATINUM(IV) COMPLEXES [J].
BRANDON, RJ ;
DABROWIAK, JC .
JOURNAL OF MEDICINAL CHEMISTRY, 1984, 27 (07) :861-865
[4]  
CHANEY SG, 1990, CANCER RES, V50, P4539
[5]   Reduction and anticancer activity of platinum(IV) complexes [J].
Choi, S ;
Filotto, C ;
Bisanzo, M ;
Delaney, S ;
Lagasee, D ;
Whitworth, JL ;
Jusko, A ;
Li, CR ;
Wood, NA ;
Willingham, J ;
Schwenker, A ;
Spaulding, K .
INORGANIC CHEMISTRY, 1998, 37 (10) :2500-2504
[6]  
CHRISTIAN MC, 1995, 7 INT S PLAT OTH MET, pS128
[7]   RELATIONSHIPS BETWEEN THE CARBON-OXYGEN STRETCHING FREQUENCIES OF CARBOXYLATO COMPLEXES AND THE TYPE OF CARBOXYLATE COORDINATION [J].
DEACON, GB ;
PHILLIPS, RJ .
COORDINATION CHEMISTRY REVIEWS, 1980, 33 (03) :227-250
[8]   PLATINUM(IV) ORGANOMETALLICS .1. SYNTHESES OF TRANS-DI(CARBOXYLATO)ETHANE-1,2-DIAMINE-CIS-BIS(PENTAFLUOROPHENYL)PLATINUM(IV) COMPLEXES AND THE X-RAY CRYSTAL-STRUCTURE OF THE N-BUTANOATO DERIVATIVE [J].
DEACON, GB ;
LAWRENZ, ET ;
HAMBLEY, TW ;
RAINONE, S ;
WEBSTER, LK .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 493 (1-2) :205-213
[9]   PREPARATIONS OF CHLORO(DIENE)POLYFLUOROPHENYLPLATINUM(II) COMPLEXES AND THE STRUCTURE OF CHLORO(DICYCLOPENTADIENE)PENTAFLUOROPHENYLPLATINUM(II) [J].
DEACON, GB ;
GATEHOUSE, BM ;
NELSONREED, KT .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1989, 359 (02) :267-283
[10]   DECARBOXYLATION SYNTHESES OF TRANSITION-METAL ORGANOMETALLICS .3. POLYFLUOROPHENYLPLATINUM(II) COMPLEXES WITH NITROGEN DONOR LIGANDS [J].
DEACON, GB ;
GRAYSON, IL .
TRANSITION METAL CHEMISTRY, 1982, 7 (02) :97-104