Biagi G - Search Results

1

Erythro- and threo-2-hydroxynonyl substituted 2-phenyladenines and 2-phenyl-8-azaadenines: ligands for A1 adenosine receptors and adenosine deaminase.

Biagi G, Giorgi I, Livi O, Pacchini F, Rum P, Scartoni V, Costa B, Mazzoni MR, Giusti L. Biagi G, et al. Farmaco. 2002 Mar;57(3):221-33. doi: 10.1016/s0014-827x(02)01200-4. Farmaco. 2002. PMID: 11989801

2

New 1,2,3-triazolo[1,5-a]quinoxalines: synthesis and binding to benzodiazepine and adenosine receptors. II.

Biagi G, Giorgi I, Livi O, Scartoni V, Betti L, Giannaccini G, Trincavelli ML. Biagi G, et al. Eur J Med Chem. 2002 Jul;37(7):565-71. doi: 10.1016/s0223-5234(02)01376-4. Eur J Med Chem. 2002. PMID: 12126775

3

Characterization and preliminary use of 1-, 2- and 3-methyl-5-phenyl-7-chloro-1,2,3-triazolo[4,5-d]pyrimidine as reaction intermediates.

Biagi G, Giorgi I, Livi O, Scartoni V, Barili PL. Biagi G, et al. Farmaco. 2003 Aug;58(8):551-6. doi: 10.1016/S0014-827X(03)00095-8. Farmaco. 2003. PMID: 12875884

4

New N6- or N(9)-hydroxyalkyl substituted 8-azaadenines or adenines as effective A1 adenosine receptor ligands.

Biagi G, Giorgi I, Leonardi M, Livi O, Pacchini F, Scartoni V, Costa B, Lucacchini A. Biagi G, et al. Eur J Med Chem. 2003 Sep;38(9):801-10. doi: 10.1016/s0223-5234(03)00147-8. Eur J Med Chem. 2003. PMID: 14561479

5

N6-cycloalkyl-2-phenyl-3-deaza-8-azaadenines: a new class of A1 adenosine receptor ligands. A comparison with the corresponding adenines and 8-azaadenines.

Biagi G, Giorgi I, Livi O, Nardi A, Pacchini F, Scartoni V, Lucacchini A. Biagi G, et al. Eur J Med Chem. 2003 Nov-Dec;38(11-12):983-90. doi: 10.1016/j.ejmech.2003.09.003. Eur J Med Chem. 2003. PMID: 14642330

6

2,9-disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: synthesis, biochemical and molecular modelling studies.

Biagi G, Bianucci AM, Coi A, Costa B, Fabbrini L, Giorgi I, Livi O, Micco I, Pacchini F, Santini E, Leonardi M, Nofal FA, Salerni OL, Scartoni V. Biagi G, et al. Bioorg Med Chem. 2005 Aug 1;13(15):4679-93. doi: 10.1016/j.bmc.2005.04.063. Bioorg Med Chem. 2005. PMID: 15908217

7

Synthesis, biological activity and molecular modelling of new trisubstituted 8-azaadenines with high affinity for A1 adenosine receptors.

Giorgi I, Bianucci AM, Biagi G, Livi O, Scartoni V, Leonardi M, Pietra D, Coi A, Massarelli I, Nofal FA, Fiamingo FL, Anastasi P, Giannini G. Giorgi I, et al. Among authors: biagi g. Eur J Med Chem. 2007 Jan;42(1):1-9. doi: 10.1016/j.ejmech.2006.08.014. Epub 2006 Oct 5. Eur J Med Chem. 2007. PMID: 17028066

8

Synthesis of new 2-phenyladenines and 2-phenylpteridines and biological evaluation as adenosine receptor ligands.

Giorgi I, Biagi G, Livi O, Leonardi M, Scartoni V, Pietra D. Giorgi I, et al. Among authors: biagi g. Arch Pharm (Weinheim). 2007 Feb;340(2):81-7. doi: 10.1002/ardp.200600168. Arch Pharm (Weinheim). 2007. PMID: 17294400

9

N6-1,3-diphenylurea derivatives of 2-phenyl-9-benzyladenines and 8-azaadenines: synthesis and biological evaluation as allosteric modulators of A2A adenosine receptors.

Giorgi I, Biagi G, Bianucci AM, Borghini A, Livi O, Leonardi M, Pietra D, Calderone V, Martelli A. Giorgi I, et al. Among authors: biagi g. Eur J Med Chem. 2008 Aug;43(8):1639-47. doi: 10.1016/j.ejmech.2007.10.021. Epub 2007 Oct 24. Eur J Med Chem. 2008. PMID: 18045744

10

Synthesis and ADA inhibitory activity of new 2-aryl-8-azaadenosines. VIII.

Biagi G, Giorgi I, Livi O, Scartoni V. Biagi G, et al. Farmaco. 1992 May;47(5):537-50. Farmaco. 1992. PMID: 1388600

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