W. Ceccarelli

Catecholic flavonoids acting as telomerase inhibitors.

J. Trosset, R. D'Alessio, D. Ballinari, 2004, Journal of medicinal chemistry.

4,5-Dihydro-1H-pyrazolo[4,3-h]quinazolines as potent and selective Polo-like kinase 1 (PLK1) inhibitors.

F. Fiorentini, M. Brasca, F. Roletto, 2010, Bioorganic & medicinal chemistry letters.

NMS-P937, a 4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline derivative as potent and selective Polo-like kinase 1 inhibitor.

F. Fiorentini, M. Brasca, E. Pesenti, 2011, Bioorganic & Medicinal Chemistry Letters.

New 13-aza baccatins

E. Arlandini, E. Vanotti, M. Menichincheri, 1997 .

Identification of 4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline derivatives as a new class of orally and selective Polo-like kinase 1 inhibitors.

D. Ballinari, V. Croci, D. Volpi, 2010, Journal of medicinal chemistry.

New rearranged products from the methylation of 13-oxobaccatin III

E. Vanotti, M. Menichincheri, N. Mongelli, 1996 .

Novel aryloxyalkylthioimidazoles as inhibitors of acyl-CoA: cholesterol-O-acyltransferase

M. Villa, M. Bani, E. Vanotti, 1995 .