Syntheses of ruthenium(II) quinonediimine complexes of cyclam and characterization of their DNA-binding activities and cytotoxicity

被引:106
作者
Chan, HL
Liu, HC
Tzeng, BLC
You, YSY
Peng, SM
Yang, MS
Che, CM
机构
[1] City Univ Hong Kong, Dept Biol & Chem, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Inst Mol Technol Drug Discovery & Synth, Dept Chem, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Inst Mol Technol Drug Discovery & Synth, Open Lab Chem Biol, Hong Kong, Hong Kong, Peoples R China
[4] Natl Taiwan Univ, Dept Chem, Taipei 10764, Taiwan
关键词
D O I
10.1021/ic0112802
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis and characterization of ruthenium(II) complexes, [Ru(cyclam)(bqdi)].ZnCl4 (1 ZnCl4; cyclam = 1,4,8,11-tetraazacyclotetradecane, bqdi = o-benzoquinonediimine), [Ru(cyclam)(nqdi)].(ClO4)(2) (2.(ClO4)(2); nqdi = 2,3-naphthoquinonediimine), and [Ru(cyclam)(phi)].(ClO4)(2) (3.(ClO4)(2); phi = 9,10-phenanthroquinonediimine), are described. The DNA binding properties and biological activity of the Ru(II) complexes were studied by various biophysical and cytological techniques. As expected, only 3 showed significant binding with DNA. The thermodynamic profile of the binding of 3 and DNA was constructed by analyzing the experimental data of absorption titration and UV melting studies with the McGhee equation, van't Hoff's equation, and the Gibbs-Helmholtz equation. Compound 3 binds double-stranded DNA with a binding constant of 5.0 x 10(4) M-1 at 20 degreesC, and the binding mode of the complex to DNA was proved to be intercalative. Cytotoxicity and induced type of cell death of 1-3 were also investigated. Basically, metal complexes with ligands of molecular shape closely related to the structure of DNA are more likely to bind DNA and possess higher toxicity.
引用
收藏
页码:3161 / 3171
页数:11
相关论文
共 63 条
[1]   ISOLATION AND GENETIC-CHARACTERIZATION OF HUMAN KB-CELL LINES RESISTANT TO MULTIPLE-DRUGS [J].
AKIYAMA, SI ;
FOJO, A ;
HANOVER, JA ;
PASTAN, I ;
GOTTESMAN, MM .
SOMATIC CELL AND MOLECULAR GENETICS, 1985, 11 (02) :117-126
[2]   INTERACTION OF ANTHRACYCLINES WITH NUCLEOTIDES AND RELATED-COMPOUNDS STUDIED BY SPECTROSCOPY [J].
BARCELO, F ;
BARCELO, I ;
GAVILANES, F ;
FERRAGUT, JA ;
YANOVICH, S ;
GONZALEZROS, JM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 884 (01) :172-181
[3]   DNA-MEDIATED PHOTOELECTRON TRANSFER-REACTIONS [J].
BARTON, JK ;
KUMAR, CV ;
TURRO, NJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (20) :6391-6393
[4]   BINDING MODES AND BASE SPECIFICITY OF TRIS(PHENANTHROLINE)RUTHENIUM(II) ENANTIOMERS WITH NUCLEIC-ACIDS - TUNING THE STEREOSELECTIVITY [J].
BARTON, JK ;
GOLDBERG, JM ;
KUMAR, CV ;
TURRO, NJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (08) :2081-2088
[5]   CHIRAL DISCRIMINATION IN THE COVALENT BINDING OF BIS(PHENANTHROLINE)DICHLORORUTHENIUM(II) TO B-DNA [J].
BARTON, JK ;
LOLIS, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (03) :708-709
[6]   METALS AND DNA - MOLECULAR LEFT-HANDED COMPLEMENTS [J].
BARTON, JK .
SCIENCE, 1986, 233 (4765) :727-734
[7]   TRIS(PHENANTHROLINE)RUTHENIUM(II) - STEREOSELECTIVITY IN BINDING TO DNA [J].
BARTON, JK ;
DANISHEFSKY, AT ;
GOLDBERG, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (07) :2172-2176
[8]   SYNTHESES AND PROPERTIES OF RUTHENIUM(II) COMPLEXES WITH OMICRON-QUINODIIMINE LIGANDS - CRYSTAL AND MOLECULAR-STRUCTURE OF RU(BPY)2(C6H4(NH)2)(PF6)2 [J].
BELSER, P ;
VONZELEWSKY, A ;
ZEHNDER, M .
INORGANIC CHEMISTRY, 1981, 20 (09) :3098-3103
[9]   SYNTHESIS AND PROPERTIES OF A NOVEL NICKEL(II) CYCLAM (CYCLAM=1,4,8,11-TETRAAZACYCLOTETRADECANE) COMPLEX COVALENTLY ATTACHED TO RU(BPY)(3)(2+) (BPY=2,2'-BIPYRIDYL) [J].
BU, XH ;
CHEN, YT ;
SHIONOYA, M ;
KIMURA, E .
POLYHEDRON, 1994, 13 (02) :325-331
[10]   Structure-based design fill of a new bisintercalating anthracycline antibiotic [J].
Chaires, JB ;
Leng, FF ;
Przewloka, T ;
Fokt, I ;
Ling, YH ;
PerezSoler, R ;
Priebe, W .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (03) :261-266