Journal article

Isolation and structural analysis of the covalent adduct formed between a bis-amino mitoxantrone analogue and DNA: A pathway to major-minor groove cross-linked adducts

SK Konda, C Kelso, J Medan, BE Sleebs, DR Phillips, SM Cutts, JG Collins

Organic and Biomolecular Chemistry | ROYAL SOC CHEMISTRY | Published : 2016

Abstract

The major covalent adduct formed between a 13C-labelled formaldehyde activated bis-amino mitoxantrone analogue (WEHI-150) and the hexanucleotide d(CG5MeCGCG)2 has been isolated by HPLC chromatography and the structure determined by NMR spectroscopy. The results indicate that WEHI-150 forms one covalent bond through a primary amine to the N-2 of the G2 residue, with the polycyclic ring structure intercalated at the 5MeC3pG4/G10p5MeC9 site. Furthermore, the WEHI-150 aromatic ring system is oriented approximately parallel to the long axis of the base pairs, with one aliphatic side-chain in the major groove and the other side-chain in the minor groove. This study indicates that mitoxantrone deri..

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University of Melbourne Researchers