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
相关论文
共 50 条
  • [41] Structure-activity relationships for inhibition of human 5α-reductases by polyphenols
    Hiipakka, RA
    Zhang, HZ
    Dai, W
    Dai, Q
    Liao, ST
    BIOCHEMICAL PHARMACOLOGY, 2002, 63 (06) : 1165 - 1176
  • [42] Structure-activity relationships in human RNA 3′-phosphate cyclase
    Tanaka, Naoko
    Shuman, Stewart
    RNA, 2009, 15 (10) : 1865 - 1874
  • [43] Odor structure-activity relationships compared in human and nonhuman primates
    Laska, M
    Trolp, S
    Teubner, P
    BEHAVIORAL NEUROSCIENCE, 1999, 113 (05) : 998 - 1007
  • [44] Structure-activity relationships of thiadiazole agonists of the human secretin receptor
    Ardecky, Robert
    Dengler, Daniela G.
    Harikumar, Kaleeckal G.
    Abelman, Mathew M.
    Zou, Jiwen
    Kramer, Bryan A.
    Ganji, Santhi Reddy
    Olson, Steve
    Ly, Alina
    Puvvula, Nikhil
    Ma, Chen-Ting
    Ramachandra, Raghuveer
    Sergienko, Eduard A.
    Miller, Laurence J.
    SLAS DISCOVERY, 2024, 29 (06)
  • [45] Human follicle-stimulating hormone structure-activity relationships
    Dias, JA
    Lindau-Shepard, B
    Hauer, C
    Auger, I
    BIOLOGY OF REPRODUCTION, 1998, 58 (06) : 1331 - 1336
  • [46] Structure-activity relationships for substrate recognition by the human dopamine transporter
    Appell, M
    Berfield, JL
    Wang, LJC
    Dunn, WJ
    Chen, NH
    Reith, MEA
    BIOCHEMICAL PHARMACOLOGY, 2004, 67 (02) : 293 - 302
  • [47] Structure-activity relationships of untenone A and its derivatives for inhibition of DNA polymerases
    Saito, F
    Takeuchi, R
    Kamino, T
    Kuramochi, K
    Sugawara, F
    Sakaguchi, K
    Kobayashi, S
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (08) : 1975 - 1977
  • [48] TOXI 2-DNA adducts of mitomycins: Structure-activity relationships
    Tomasz, Maria
    Basu, Ashis K.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 232
  • [49] Inhibition of DNA synthesis by hydroxyureas and related compounds: Structure-activity relationships
    Mandloi, M
    Karmarkar, S
    Joshi, S
    Khadikar, PV
    OXIDATION COMMUNICATIONS, 2001, 24 (02): : 291 - 301
  • [50] Structure-Activity Relationships in Metal-Binding Pharmacophores for Influenza Endonuclease
    Credille, Cy V.
    Dick, Benjamin L.
    Morrison, Christine N.
    Stokes, Ryjul W.
    Adamek, Rebecca N.
    Wu, Nicholas C.
    Wilson, Ian A.
    Cohen, Seth M.
    JOURNAL OF MEDICINAL CHEMISTRY, 2018, 61 (22) : 10206 - 10217