Kempen Isabelle, Hemmer Marc, Counerotte Stéphane, Pochet Lionel, de Tullio Pascal, Foidart Jean-Michel, Blacher Silvia, Noël Agnès, Frankenne Francis, Pirotte Bernard
Drug Research Center, Laboratoire de Chimie Pharmaceutique, Université de Liège, 1 Avenue de l'Hôpital, tour 4 (+5), Sart-Tilman, B-4000 Liège, Belgium.
Eur J Med Chem. 2008 Dec;43(12):2735-50. doi: 10.1016/j.ejmech.2008.01.024. Epub 2008 Jan 31.
Novel 6-substituted 2-oxo-2H-1-benzopyran-3-carboxylic acid derivatives were synthesized and their potency in reducing the invasive behaviour of HT 1080 fibrosarcoma cells was evaluated. Structure-activity relationships were deduced from biological results and will be used in further design of new active compounds. In particular, the acetoxymethyl substituent found at the 6-position of previously described active compounds can be replaced by an acetamidomethyl substituent without loss of potency; while the presence of an aryl ester function at the 3-position was preferred to a thioester or an amide function to induce marked biological activity. This work confirms the interest of aryl esters of 6-substituted coumarin-3-carboxylic acids as potential new anti-cancer agents.