Cytotoxic platinum(II) intercalators that incorporate 1R,2R-diaminocyclopentane

被引:46
作者
Garbutcheon-Singh, K. Benjamin [1 ]
Leverett, Peter [1 ]
Myers, Simon [1 ,2 ]
Aldrich-Wright, Janice R. [1 ]
机构
[1] Univ Western Sydney, Sch Sci & Hlth, Nanoscale Org & Dynam Grp, Penrith, NSW 2751, Australia
[2] Univ Western Sydney, Sch Med, Penrith, NSW 2751, Australia
关键词
SUBSTITUTED 1,10-PHENANTHROLINES; METALLOINTERCALATION REAGENTS; BIOLOGICAL-ACTIVITY; COMPLEXES; DNA;
D O I
10.1039/c2dt31323e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Twelve metallointercalators of the type [Pt(IL)(AL)](2+), where A(L) is either the R,R or S,S enantiomer of 1,2-diaminocyclopentane (DACP) and IL is either 1,10-phenathroline, 4-methyl-1,10-phenanthroline, 5-methyl-1,10-phenanthroline, 4,7-dimethyl-1,10-phenanthroline, 5,6-dimethyl-1,10-phenanthroline or 3,4,7,8-tetramethyl-1,10-phenanthroline, were synthesised, characterised and the cytotoxicity to the L1210 cell line was determined. The crystal structures of PHENRRDACP and PHENSS were obtained as monoclinic with a space group of P2(1) (a/angstrom = 11.4966, b/angstrom = 6.6983, c/angstrom = 12.0235) and P2(1) (a/angstrom = 11.5777, b/angstrom = 7.0009, c/angstrom = 12.5079), respectively. The R, R enantiomer of 1,2-diaminocyclopentane (RRDACP) produced the most cytotoxic metallointercalators. The most cytotoxic metallointercalators were 56MERRDACP and 47MERRDACP with IC50 values of 0.16 and 0.17 mu M, respectively, in comparison to cisplatin (1 mu M).
引用
收藏
页码:918 / 926
页数:9
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