Brevetto n. US9133197, OXIDATED DERIVATIVES OF TRIAZOLYLPURINES USEFUL AS LIGANDS OF THE ADENOSINE A2A RECEPTOR AND THEIR USE AS MEDICAMENTS.
Cabri w, Present and Future of Industrial Pharmaceutical Industries in Italy, «LA CHIMICA E L'INDUSTRIA», 2010, 76, pp. 84 - 85 [articolo]
D'Acquarica I; Gasparrini F; Kotoni D; Pierini M; Villani C; Cabri W; Di Mattia M; Giorgi F, Stereodynamic Investigation of Labile Stereogenic Centres in Dihydroartemisinin, «MOLECULES», 2010, 15, pp. 1309 - 1323 [articolo]
I. D'Aquarica; F.Gasparrini; D.Kotoni; M.Pierini; M.Piras; C.Villani;W.Cabri;M.Di Mattia; F.Giorgi; A.Mazzanti, Stereolability of MKA, a rearrangement product of dihydroartemisinin endowed with antimalarian activity, in: AA.VV., Atti del Convegno, ROMA, Società Chimica Italiana, 2010, 1, pp. P93 - P93 (atti di: XXXIII Convegno Nazionale della Divisione di Chimica Organica, S.Benedetto del Tronto, 12-16 settembre 2010) [atti di convegno-abstract]
Brevetto n. US7799921, Stereoselective process and crystalline forms of a camptothecin.
Brevetto n. US81247769, Stereoselective process and crystalline forms of a camptothecin.
Hanessian S; Auzzas L; Larsson A; Zhang JB; Giannini G; Gallo G; Ciacci A; Cabri W, Vorinostat-Like Molecules as Structural, Stereochemical, and Pharmacological Tools, «ACS MEDICINAL CHEMISTRY LETTERS», 2010, 1, pp. 70 - 74 [articolo]
P. Galletti; A. Quintavalla; C. Ventrici; G. Giannini; W. Cabri; D. Giacomini, 2-Azetidinones: synthesis of new bis(indolyl)butyl-beta-lactams, «NEW JOURNAL OF CHEMISTRY», 2010, 34, pp. 2861 - 2866 [articolo]
Brevetto n. US8383616, Aryl isoxazole compounds with antitumoral Activities.
P. Galletti; A. Quintavalla; C. Ventrici; G. Giannini; W. Cabri; S. Penco; G. Gallo; S. Vincenti; D. Giacomini, Azetidinones as Zinc-Binding Groups to Design Selective HDAC8 Inhibitors, «CHEMMEDCHEM», 2009, 4, pp. 1991 - 2001 [articolo]
Cabri W, Catalysis: The pharmaceutical perspective, «CATALYSIS TODAY», 2009, 140, pp. 2 - 10 [replica/breve intervento]
Giannini G.; Marzi M.; Pezzi R.; Brunetti T.; Battistuzzi G.; Marzo M.D.; Cabri W.; Vesci L.; Pisano C., Corrigendum to "N-Hydroxy-(4-oxime)-cinnamide: A versatile scaffold for the synthesis of novel histone deacetilase (HDAC) inhibitors" [Bioorg. Med. Chem. Lett. 19 (2009) 2346] (DOI:10.1016/j.bmcl.2009.02.029), «BIOORGANIC & MEDICINAL CHEMISTRY LETTERS», 2009, 19, pp. 3694 - 3694 [articolo]
Brevetto n. US8865597, Crystalline(6R,7R)-7-[1,2,4]triazolo-3-yl)-2-[(Z)-trityloxyimino]-acety-lamino)- 3-[(R)-1’-tert-butoxycarbonyl-2-oxo-[1,3’]bipyrrolidinyl-(3E)ylidenemethyl-8-oxo- 5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydril ester; its manufacturing and use.
Brevetto n. WO2009109504, Enol carbamate derivatives as modulators of fatty Acid Amide Hydrolase.
Giannini G; Marzi M; Di Marzo M; Battistuzzi G; Pezzi R; Brunetti T; Cabri W; Vesci L; Pisano C, Exploring bis-(indolyl)methane moiety as an alternative and innovative CAP group in the design of histone deacetylase (HDAC) inhibitors, «BIOORGANIC & MEDICINAL CHEMISTRY LETTERS», 2009, 19, pp. 2840 - 2843 [articolo]
