Molecular Basis of Structure-Activity Relationships between Salphen Metal Complexes and Human Telomeric DNA Quadruplexes

被引:191
|
作者
Campbell, Nancy H. [1 ]
Abd Karim, Nurul H. [2 ]
Parkinson, Gary N. [1 ]
Gunaratnam, Mekala [1 ]
Petrucci, Vanessa [1 ]
Todd, Alan K. [1 ]
Vilar, Ramon [2 ]
Neidle, Stephen [1 ]
机构
[1] Univ London, Sch Pharm, CRUK Biomol Struct Grp, London WC1N 1AX, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
CRYSTAL-STRUCTURES; SQUARE-PLANAR; INHIBITION; STABILIZATION; RECOGNITION; SELECTIVITY; GEOMETRY; ASSAY;
D O I
10.1021/jm201140v
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The first X-ray crystal structures of nickel(II) and copper(II) salphen metal complexes bound to a quadruplex DNA are presented. Two structures have been determined and show that these salphen-metal complexes bind to human telomeric quadruplexes by end-stacking, with the metal in each case almost in line with the potassium ion channel. Quadruplex and duplex DNA binding is presented for these two and other related salphen complexes, all with side-chains terminating in pyrrolidino end-groups and differing patterns of substitution on the salphen core. The crystal structures are able to provide rationalizations for the structure-activity data, and in particular for the superior quadruplex-binding of the nickel complexes compared to that of the copper-containing ones. The complexes show significant antiproliferative activity for the compounds in a panel of cancer cell lines. They also show telomerase inhibitory activity in the telomerase TRAP-LIG assay.
引用
收藏
页码:209 / 222
页数:14
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