Inhibition of growth of B16 murine melanoma cells by novel spermine analogues

S. Carrington, M. A. Qarawi, I. S. Blagbrough, S. H. Moss, C. W. Pouton

Research output: Contribution to journalArticleResearchpeer-review

1 Citation (Scopus)

Abstract

To develop new cytotoxins, which could find use as anti-cancer agents, polyamine conjugates were synthesized containing spermine and an anthracene or acridine unit. Spermine is known to groove-bind to DNA; anthracene and acridine are known to intercalate. It was hoped that these polyamine-polyaromatic conjugates would use both modes of binding. Studies of growth inhibition of B16 murine melanoma cells showed the conjuates to be more effective than either spermine, anthracene-9-carboxylic acid or acridine-9-carboxylic acid, and of the conjugates, the acridine derivative showed greatest activity.

Original languageEnglish
Pages (from-to)25-27
Number of pages3
JournalPharmaceutical Sciences
Volume2
Issue number1
Publication statusPublished - 1 Dec 1996

Cite this