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Results: 1-8 |
Results: 8
Design, synthesis, and characterization of the antitumor activity of novelceramide analogues
Authors: Macchia, M Barontini, S Bertini, S Di Bussolo, V Fogli, S Giovannetti, E Grossi, E Minutolo, F Danesi, R
Citation: M. Macchia et al., Design, synthesis, and characterization of the antitumor activity of novelceramide analogues, J MED CHEM, 44(23), 2001, pp. 3994-4000
Purification, enzymatic characterization, and inhibition of the Z-farnesyldiphosphate synthase from Mycobacterium tuberculosis
Authors: Schulbach, MC Mahapatra, S Macchia, M Barontini, S Papi, C Minutolo, F Bertini, S Brennan, PJ Crick, DC
Citation: Mc. Schulbach et al., Purification, enzymatic characterization, and inhibition of the Z-farnesyldiphosphate synthase from Mycobacterium tuberculosis, J BIOL CHEM, 276(15), 2001, pp. 11624-11630
Polyprenyl phosphate biosynthesis in Mycobacterium tuberculosis and Myobacterium smegmatis
Authors: Crick, DC Schulbach, MC Zink, EE Macchia, N Barontini, S Besra, GS Brennan, PJ
Citation: Dc. Crick et al., Polyprenyl phosphate biosynthesis in Mycobacterium tuberculosis and Myobacterium smegmatis, J BACT, 182(20), 2000, pp. 5771-5778
New N-substituted 7-aminocephalosporanic acid derivatives as potential agents against Streptococcus pneumoniae. Synthesis and in vitro activity
Authors: Balsamo, A Barontini, S Calvani, F Gentili, D Macchia, M Rossello, A Di Modugno, E Felici, A
Citation: A. Balsamo et al., New N-substituted 7-aminocephalosporanic acid derivatives as potential agents against Streptococcus pneumoniae. Synthesis and in vitro activity, BIOORG MED, 9(7), 1999, pp. 1035-1040
An unexpected result in the condensation of 2-amino-6-bromo-pyridine with ethyl 4-chloroacetoacetate: Four dihalo-substituted pyrido[1,2-a]pyrimidin-4-ones as reaction products
Authors: Ferrarini, PL Mori, C Mori, F Saccomanni, G Barontini, S Macchia, M Barili, PL Hamdan, M
Citation: Pl. Ferrarini et al., An unexpected result in the condensation of 2-amino-6-bromo-pyridine with ethyl 4-chloroacetoacetate: Four dihalo-substituted pyrido[1,2-a]pyrimidin-4-ones as reaction products, J HETERO CH, 36(4), 1999, pp. 1065-1072
Synthesis and HIV-1 inhibitory properties of new tetrahydrobenzoquinazolinedione and tetrahydrobenzocycloheptenuracil derivatives and of their thioxoanalogues
Authors: Macchia, N Antonelli, G Balsamo, A Barontini, S Calvani, F Gentili, P Martinelli, D Rossello, A Turriziani, O Tesoro, J
Citation: N. Macchia et al., Synthesis and HIV-1 inhibitory properties of new tetrahydrobenzoquinazolinedione and tetrahydrobenzocycloheptenuracil derivatives and of their thioxoanalogues, FARMACO, 54(4), 1999, pp. 242-247
Fluorescent probes for adenosine receptors: Synthesis and biology of N-6-dansylaminoalkyl-substituted NECA derivatives
Authors: Macchia, M Salvetti, F Barontini, S Calvani, F Gesi, M Hamdan, M Lucacchini, A Pellegrini, A Soldani, P Martini, C
Citation: M. Macchia et al., Fluorescent probes for adenosine receptors: Synthesis and biology of N-6-dansylaminoalkyl-substituted NECA derivatives, BIOORG MED, 8(22), 1998, pp. 3223-3228
Toward the rational development of peptidomimetic analogs of the C-terminal endothelin hexapeptide: development of a theoretical model
Authors: Macchia, M Barontini, S Ceccarelli, F Galoppini, C Giusti, L Hamdan, M Lucacchini, A Martinelli, A Menchini, E Mazzoni, MR Revoltella, RP Romagnoli, F Rovero, P
Citation: M. Macchia et al., Toward the rational development of peptidomimetic analogs of the C-terminal endothelin hexapeptide: development of a theoretical model, FARMACO, 53(8-9), 1998, pp. 545-556
Risultati: 1-8 |