Sfoglia per Autore
Importance of the Substituent on C(2) in the Interconversion of the Thiazine and the Thiazolidine System of b-Lactam Antibiotics
1980-01-01 Balsamo, A; Domiano, P; Giorgi, Irene; Nannini, G; Macchia, B; Macchia, F; Rosai, A.
Chemistry of the Dihydrothiazine Ring Moiety of Cephalosporins. A Route to 3-Formoxymethyl-3-Cephem Derivatives
1981-01-01 Balsamo, A; Epifani, E; Giorgi, Irene; Lapucci, Annalina; Macchia, B; Macchia, F.
Interconversion of the thiazine and thiazolidine system of β -lactam antibiotics. Electrochemical cleavage of Kamiya's disulfide promoted by bromide ion
1982-01-01 Balsamo, A; Bedini, Pm; Giorgi, Irene; Macchia, B; Macchia, F.
3-[(2-Ethoxyphenoxy)methyl]piperidine derivatives. Synthesis and antidepressant activity
1987-01-01 Balsamo, A; Giorgi, Irene; Lapucci, Annalina; Lucacchini, Antonio; Macchia, B; Macchia, F; Martini, Claudia; Rossi, A.
Modification of the 1,2,3-Triazole Ring Present in an Effective in vitro Inhibitor of Prostaglandin Synthesis
1989-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V; Andreini, F.
XANTHINE-OXIDASE INHIBITION - EFFECT OF AN N-ALKYL SUBSTITUENT ON C-2 OF THE NUCLEUS OF 8-AZAHYPOXANTHINE
1989-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V; Lucacchini, Antonio
"One Pot" Synthesis of 2-Substituted 9-(2'-Hydroxy-3'-aminopropyl)-8-azahypoxanthines and 8-Azaadenines [5-Substituted 3-(2'-Hydroxy-3'-aminopropyl)-7-amino and 7-hyroxy- 3H-1,2,3-triazolo[4,5-d]pyrimidines]
1989-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V; Franchi, M.
Xanthine Oxidase Inhibition: Effect of a Linear Carboalkoxy Substituent on C(2) of the Nucleus of 8-Azahypoxanthine
1990-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V; Tonetti, I; Lucacchini, Antonio
In vitro Inhibitors of Prostaglandin Synthesis: (p-Thiosubstituted)-Benzyl Nitrogen Heterocycles
1990-01-01 Biagi, G; Dell'Omodarme, G; Giorgi, Irene; Livi, O; Scartoni, V.
Studies on 1,2,3-Triazole Derivatives as in vitro Inhibitors of Prostaglandine Synthesis
1990-01-01 Biagi, G; Ferretti, M; Dell'Omodarme, G; Giorgi, Irene; Livi, O; Scartoni, V.
Vehicle influence on the permeation of a highly lipophilic molecule. An in vitro technique to evaluate skin-vehicle interactions
1990-01-01 Nannipieri, E.; Carelli, V.; DI COLO, G; Giorgi, Irene; Serafini, M. F.
A Method for the Synthesis of Racemic and Optically Active 2-Substituted 9-(2',3'-Dihidroxypropyl)-8-Azahypoxanthines and 8-Azaadenines
1991-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V; Barili, Pl
An 1,2,3,Triazole Derivatives Bioisoster of a Potent in vitro Prostaglandin Synthesis Inhibitor: Preparation and Biological Activity
1992-01-01 Biagi, G; Dell'Omodarme, G; Giorgi, Irene; Livi, O; Scartoni, V.
Structure-Activity Studies on a 1,2,3-Triazole Derivative, a Potent in vitro Inhibitor of Prostaglandin Synthesys: the Role of the Heterocyclic Ring
1992-01-01 Biagi, G; Dell'Omodarme, G; Giorgi, Irene; Ferretti, M; Livi, O; Scartoni, V.
Synthesis of New 2-Substituted 9-?-D-Ribofuranosyl-8-Azahypoxanthine
1992-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V.
Synthesis and ADA Inhibitory Activity of New 2-Aryl-8-Azaadenosines
1992-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V.
Evaluation of the Quantitative Contribution of a Phenyl Group on C(2) of 8-Azaadenosine to the Binding with Adenosine Deaminase: a New Synthesis of 8-Azaadenosine. XI.
1992-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V; Lucacchini, Antonio
An 1,2,3-Triazole Derivative Bioisoster of a Potent in Vitro Prostaglandin Synthesis Inhibitor: Preparation and Biological Activity
1992-01-01 Biagi, Giuliana; Dell'Omodarme, Giuliana; Giorgi, Irene; Livi, Oreste; Scartoni, Valerio
1,2,3-Trizoles[4,5-d]piridazines. Analogues of Prostaglandin Synthesis Inhibitors
1993-01-01 Biagi, G; Ferretti, G; Giorgi, Irene; Livi, O; Scartoni, V; Lucacchini, Antonio
Xanthine Oxidase (XO): Relative Configuration of Complexes Formed by the Enzyme, 2- or 8-n-Alkyl-hypoxanthines and 2-n-Alkyl-8-azahypoxanthines. XII
1993-01-01 Biagi, G; Giorgi, Irene; Livi, O; Scartoni, V; Lucacchini, Antonio; Tonetti, I.
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