Angela, Rampa; Francesca, Mancini; Angela, De Simone; Federico, Falchi; Federica, Belluti; Rita Maria, Concetta Di Martino; Silvia, Gobbi; Vincenza, Andrisano; Andrea, Tarozzi; Manuela, Bartolini; Andrea, Cavalli; Alessandra, Bisi, From AChE to BACE1 inhibitors: The role of the amine on the indanone scaffold, «BIOORGANIC & MEDICINAL CHEMISTRY LETTERS», 2015, 25, pp. 2804 - 2808 [articolo]
Gobbi S;Rampa A;Belluti F;Bisi A, Nonsteroidal aromatase inhibitors for the treatment of breast cancer: an update., «ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY», 2014, 14, pp. 54 - 65 [articolo]
A. Bisi;S. Gobbi;F. Belluti;A. Rampa, Design of Multifunctional Compounds for Cardiovascular Disease: From Natural Scaffolds to “Classical” Multitarget Approach, «CURRENT MEDICINAL CHEMISTRY», 2013, 20, pp. 1759 - 1782 [articolo]
Federica Belluti;Remo Perozzo;Leonardo Lauciello;Francesco Colizzi;Dirk Kostrewa;Alessandra Bisi;Silvia Gobbi;Angela Rampa;Maria Laura Bolognesi;Maurizio Recanatini;Reto Brun;Leonardo Scapozza;Andrea Cavalli, Design, Synthesis, and Biological and Crystallographic Evaluation of Novel Inhibitors ofPlasmodium falciparumEnoyl-ACP-reductase (PfFabI), «JOURNAL OF MEDICINAL CHEMISTRY», 2013, 56, pp. 7516 - 7526 [articolo]
Rampa A;Gobbi S;Belluti F;Bisi A, Emerging targets in neurodegeneration: new opportunities for Alzheimer's disease treatment?, «CURRENT TOPICS IN MEDICINAL CHEMISTRY», 2013, 13, pp. 1879 - 1904 [articolo]
Silvia Gobbi;Qingzhong Hu;Matthias Negri;Christina Zimmer;Federica Belluti;Angela Rampa;Rolf W. Hartmann;Alessandra Bisi, Modulation of Cytochromes P450 with Xanthone-Based Molecules: From Aromatase to Aldosterone Synthase and Steroid 11β-Hydroxylase Inhibition, «JOURNAL OF MEDICINAL CHEMISTRY», 2013, 56, pp. 1723 - 1729 [articolo]
Rampa A; Bisi A, New approaches to the treatment of Alzheimer's disease., «CURRENT TOPICS IN MEDICINAL CHEMISTRY», 2013, 13, pp. 1743 - 1744 [replica/breve intervento]
Federica Belluti;Angela Rampa;Silvia Gobbi;Alessandra Bisi, Small-molecule inhibitors/modulators of amyloid-β peptide aggregation and toxicity for the treatment of Alzheimer's disease: a patent review (2010 – 2012), «EXPERT OPINION ON THERAPEUTIC PATENTS», 2013, 23, pp. 581 - 596 [articolo]
A. Rampa; M. Bartolini; A. Bisi; F. Belluti; S. Gobbi; V. Andrisano; A. Ligresti; V. Di Marzo, The first dual ChE/FAAH inhibitors: new perspectives for
Alzheimer's disease?, «ACS MEDICINAL CHEMISTRY LETTERS», 2012, 3, pp. 182 - 186 [articolo]
S. Rizzo; A. Tarozzi; M. Bartolini; G. Da Costa; A. Bisi; S. Gobbi; F. Belluti; A. Ligresti; M. Allarà; J-P. Monti; V. Andrisano; V. Di Marzo; P. Hrelia; A. Rampa, 2-Arylbenzofuran-based molecules as multipotent Alzheimer's disease modifying agents, «EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY», 2012, 58, pp. 519 - 532 [articolo]
F. Belluti; M. Bartolini; G. Bottegoni; A. Bisi; A. Cavalli; V. Andrisano; A. Rampa, Benzophenone-based derivatives: A novel series of potent and selective dual inhibitors of acetylcholinesterase and acetylcholinesterase-induced
beta-amyloid aggregation, «EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY», 2011, 46, pp. 1682 - 1693 [articolo]
A. Rampa; F. Belluti; S. Gobbi; A. Bisi, Hybrid-Based Multi-Target Ligands for the Treatment of Alzheimer's Disease, «CURRENT TOPICS IN MEDICINAL CHEMISTRY», 2011, 11, pp. 2716 - 2730 [articolo]
S. Rizzo; A. Bisi; M. Bartolini; F. Mancini; F. Belluti; S. Gobbi; V. Andrisano; A. Rampa, Multi-target strategy to address Alzheimer’s disease: Design, synthesis and biological evaluation of new tacrine-based dimers, «EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY», 2011, 46, pp. 4336 - 4343 [articolo]
Gobbi S.; Zimmer C.; Belluti F.; Rampa A.; Hartmann R.W.; Recanatini M.; Bisi A., Novel highly potent and selective nonsteroidal aromatase inhibitors: synthesis, biological evaluation and structure-activity relationships investigation, «JOURNAL OF MEDICINAL CHEMISTRY», 2010, 53, pp. 5347 - 5351 [articolo]
S. Bova; S. Saponara; A. Rampa; S. Gobbi; L. Cima; F. Fusi; G. Sgaragli; M. Cavalli; C. de los Rios; J. Striessnig; A. Bisi, Anthracene Based Compounds as New L-type
Ca2+ Channel Blockers: Design, Synthesis,
and Full Biological Profile, «JOURNAL OF MEDICINAL CHEMISTRY», 2009, 52, pp. 1259 - 1262 [articolo]