Benzodipyrazoles: a new class of potent CDK2 inhibitors.
暂无分享,去创建一个
Anna Vulpetti | Alexander Cameron | Roberto D'Alessio | A. Vulpetti | R. D'Alessio | P. Pevarello | M. Brasca | F. Roletto | A. Cameron | A. Marsiglio | Paolo Pevarello | Fulvia Roletto | Aurelio Marsiglio | M. Vazquez | S. Metz | Michael L Vazquez | P. Polucci | Alberto Bargiotti | Suzanne Metz | M Gabriella Brasca | Antonella Ermoli | Paolo Polucci | Marcellino Tibolla | A. Bargiotti | M. Tibolla | A. Ermoli
[1] Nader Fotouhi,et al. Cell cycle inhibitors for the treatment of cancer , 2003 .
[2] S. Knapp,et al. Structural characterization of the GSK-3beta active site using selective and non-selective ATP-mimetic inhibitors. , 2003, Journal of molecular biology.
[3] G. Stein. The molecular basis of cell cycle and growth control , 1999 .
[4] A. Huwe,et al. Small molecules as inhibitors of cyclin-dependent kinases. , 2003, Angewandte Chemie.
[5] E. Sausville. Cyclin-dependent kinase modulators studied at the NCI: pre-clinical and clinical studies. , 2003, Current medicinal chemistry. Anti-cancer agents.
[6] P. Fischer,et al. CDK inhibitors in clinical development for the treatment of cancer , 2003, Expert opinion on investigational drugs.