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Identification of substituted pyrazolo[1,5-a]quinazolin-5(4H)-one as potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors
Authors:Federica Orvieto  Danila Branca  Claudia Giomini  Philip Jones  Uwe Koch  Jesus M. Ontoria  Maria Cecilia Palumbi  Michael Rowley  Carlo Toniatti  Ester Muraglia
Affiliation:IRBM - Merck Research Laboratories Rome, Via Pontina km 30,600, Pomezia, 00040 Rome, Italy
Abstract:A novel series of pyrazolo[1,5-a]quinazolin-5(4H)-one derivatives proved to be a potent class of PARP-1 inhibitors. An extensive SAR around the 3-position of pyrazole in the scaffold led to the discovery of amides derivatives as low nanomolar PARP-1 inhibitors.
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