IMIS | Flanders Marine Institute
 

Flanders Marine Institute

Platform for marine research

IMIS

Publications | Institutes | Persons | Datasets | Projects | Maps
[ report an error in this record ]basket (0): add | show Printer-friendly version

Synthesis and in vitro antiproliferative activity of amido and amino analogues of the marine alkaloid isogranulatimide
Lavrard, H; Salvetti, B; Mathieu, V.; Rodriguez, F; Kiss, R.; Delfourne, E (2015). Synthesis and in vitro antiproliferative activity of amido and amino analogues of the marine alkaloid isogranulatimide. ChemMedChem 10(4): 607-609. dx.doi.org/10.1002/cmdc.201500025
In: ChemMedChem: Chemistry Enabling Drug Discovery. Wiley: Oxford. ISSN 1860-7179, more

Available in Authors 

Keyword
    Marine
Author keywords
    antiproliferative agents; granulatimide; isogranulatimide; marinealkaloids; natural products

Authors  Top 
  • Lavrard, H
  • Salvetti, B
  • Mathieu, V.
  • Rodriguez, F
  • Kiss, R.
  • Delfourne, E

Abstract
    Marine organisms have proven to be a promising source of new compounds with activity against tumor cell lines. Granulatimide and isogranulatimide are marine alkaloids that have been shown to inhibit checkpoint kinase 1 (Chk1), a key protein in the DNA damage response and an emerging target for anticancer therapeutics. Here, we describe the synthesis and preliminary evaluation of amido and amino analogues of isogranulatimide. The new derivatives were prepared in three steps from 2-imidazol-1-yl-1H-indol-5-ylamine. Two of the compounds synthesized exhibited more potent in vitro antiproliferative activity (single-digit micromolar concentration range), by at least one log of magnitude, than the natural product isogranulatimide when evaluated in six human tumor cell lines: non-small-cell lung cancer (A549), colon cancer (LoVo), breast cancer (MCF7), oligodendroglioma (Hs683), glioblastoma (U373), and melanoma (SKMEL28). The mechanism of action of these derivatives remains to be elucidated, given that they did not significantly inhibit Chk1, however these compounds are easily synthesized and exhibit potent anticancer activity and are thus worthy of further study.

All data in IMIS is subject to the VLIZ privacy policy Top | Authors