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

K. Benjamin Garbutcheon-Singh, Peter Leverett, Simon Myers, Janice R. Aldrich-Wright

    Research output: Contribution to journalArticlepeer-review

    Abstract

    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 µM, respectively, in comparison to cisplatin (1 µM).
    Original languageEnglish
    Pages (from-to)918-926
    Number of pages9
    JournalDalton Transactions
    Volume42
    Issue number4
    DOIs
    Publication statusPublished - 2013

    Keywords

    • DNA
    • biological activity
    • cancer
    • complexes
    • metallointercalators

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