作者:Patrizia Diana、Paola Barraja、Antonino Lauria、Anna Maria Almerico、Girolamo Cirrincione、Anna Giulia Loi、Chiara Musiu、Alessandra Pani、Paolo La Colla、Maria Elena Marongiu
DOI:10.1016/s0223-5234(99)80085-3
日期:1999.4
2-Triazenopyrroles were synthesized by coupling the corresponding 2-diazopyrroles with secondary amines and tested for antiproliferative, antifungal, antiviral and antibacterial activities. Derivative 9m was the most cytotoxic, showing, against leukaemia, lymphoma and carcinoma cell lines, IC50 3.9-21 mu M and inhibited Cox-B2 and VSV with EC50 10 mu M. Derivative 9j, instead, was active against C. albicans with a selectivity index higher than that of miconazole. (C) Elsevier, Paris.