Synthesis, Mechanism of Action, and Biological Evaluation of Mitosenes

E. O.M. Orlemans, W. Verboom, M. W. Scheltinga, D. N. Reinhoudt*, P. Lelieveld, H. H. Fiebig, B. R. Winterhalter, J. A. Double, M. C. Bibby

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    92 Citations (Scopus)
    217 Downloads (Pure)


    Mitosenes of both the pyrrolo- and pyrido[l,2-a]indole type have been prepared via modification of these heterotricyclic compounds. Several mitosenes have been studied for their reactions with nucleophiles under reductive conditions. The results of these experiments show that the biological activity of mitosenes is based on the mechanism of bioreductive activation. When both leaving groups at C-l and C-10 in the mitosene are the same, the nucleophile preferably adds to C-10 under reductive conditions. All mitosenes were studied for their biological activities in vitro against L1210, WiDr, and A204. On the basis of these results a selection of three mitosenes was made for a more detailed biological evaluation. Several tumor model systems were used, viz. P388, human tumor xenografts, MAC 13, and MAC 16. The results of these studies show that mitosenes have a more limited range of activities than mitomycin C. Surprisingly, the in vivo activities of mitosene diol 8b and mitosene diacetate 10b against the gastric human tumor xenograft GXF 97 were very high and comparable with that of mitomycin C.

    Original languageEnglish
    Pages (from-to)1612-1620
    Number of pages9
    JournalJournal of medical chemistry
    Issue number7
    Publication statusPublished - 1 Jul 1989


    Dive into the research topics of 'Synthesis, Mechanism of Action, and Biological Evaluation of Mitosenes'. Together they form a unique fingerprint.

    Cite this