Matteo D’Anello

Discovery of 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro-1<i>H</i>-isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and Highly Selective PARP-1 Inhibitor for Cancer Therapy

Gianluca Papeo, Helena Posteri, Daniela Borghi et al. · Journal of Medicinal Chemistry · 2015 · 143 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +13

Cdc7 Kinase Inhibitors: 5-Heteroaryl-3-Carboxamido-2-Aryl Pyrroles as Potential Antitumor Agents. 1. Lead Finding

Maria Menichincheri, Clara Albanese, Cristina Alli et al. · Journal of Medicinal Chemistry · 2010 · 62 citations · Full text

Pharmacy, Medicinal Chemistry, Oncology +16

Discovery and optimization of pyrrolo[1,2-a]pyrazinones leads to novel and selective inhibitors of PIM kinases

Francesco Casuscelli, Elena Ardini, Nilla Avanzi et al. · Bioorganic & Medicinal Chemistry · 2013 · 37 citations · Full text

Pharmacy, Medicinal Chemistry, Pharmacology +13

Thieno[3,2-c]pyrazoles: A novel class of Aurora inhibitors with favorable antitumor activity

Simona Bindi, Daniele Fancelli, Cristina Alli et al. · Bioorganic & Medicinal Chemistry · 2010 · 28 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +8

5‐Oxazolones, II. 2,4‐Diaryl‐4‐(2,4‐dinitroaryl)‐5(4<i>H</i>)‐oxazolones: Synthesis and Acid‐Catalyzed Transformation into 1‐Hydroxy‐1<i>H</i>‐indazole Derivatives

Matteo D’Anello, Emanuela Erba, Maria Luisa Gelmi et al. · Chemische Berichte · 1988 · 22 citations

Natural Sciences, Chemistry, Medicinal Chemistry +9