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 language | English |
|---|---|
| Pages (from-to) | 918-926 |
| Number of pages | 9 |
| Journal | Dalton Transactions |
| Volume | 42 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2013 |
Keywords
- DNA
- biological activity
- cancer
- complexes
- metallointercalators
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