Giorgi I - Search Results

1

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. Among authors: giorgi i. Farmaco. 2003 Aug;58(8):551-6. doi: 10.1016/S0014-827X(03)00095-8. Farmaco. 2003. PMID: 12875884

2

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. Among authors: giorgi i. Farmaco. 2002 Mar;57(3):221-33. doi: 10.1016/s0014-827x(02)01200-4. Farmaco. 2002. PMID: 11989801

3

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. Among authors: giorgi i. 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

4

1,5-Diarylsubstituted 1,2,3-triazoles as potassium channel activators. VI.

Biagi G, Calderone V, Giorgi I, Livi O, Martinotti E, Martelli A, Nardi A. Biagi G, et al. Among authors: giorgi i. Farmaco. 2004 May;59(5):397-404. doi: 10.1016/j.farmac.2004.01.012. Farmaco. 2004. PMID: 15120319

5

1,4- and 2,4-substituted-1,2,3-triazoles as potential potassium channel activators. VII.

Calderone V, Giorgi I, Livi O, Martinotti E, Martelli A, Nardi A. Calderone V, et al. Among authors: giorgi i. Farmaco. 2005 May;60(5):367-75. doi: 10.1016/j.farmac.2005.03.004. Farmaco. 2005. PMID: 15910810 Review.

6

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

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

7

Structure-activity studies on a 1,2,3-triazole derivative, a potent in vitro inhibitor of prostaglandin synthesis: the role of the heterocyclic ring.

Biagi G, Dell'Omodarme G, Ferretti M, Giorgi I, Livi O, Scartoni V. Biagi G, et al. Among authors: giorgi i. Farmaco. 1992 Mar;47(3):335-44. Farmaco. 1992. PMID: 1503597

8

An 1,2,3-triazole derivative bioisoster of a potent in vitro prostaglandin synthesis inhibitor: preparation and biological activity.

Biagi G, Dell'Omodarme G, Giorgi I, Livi O, Scartoni V, Di Bussolo V. Biagi G, et al. Among authors: giorgi i. Farmaco. 1992 Jan;47(1):91-8. Farmaco. 1992. PMID: 1616580

9

In vitro inhibitors of prostaglandin synthesis: (p-thiosubstituted)-benzyl nitrogen heterocycles.

Biagi G, Dell'Omodarme G, Giorgi I, Livi O, Scartoni V. Biagi G, et al. Among authors: giorgi i. Farmaco. 1990 Sep;45(9):989-99. Farmaco. 1990. PMID: 2126438

10

Studies on 1,2,3-triazole derivatives as in vitro inhibitors of prostaglandin synthesis.

Biagi G, Dell'Omodarme G, Ferretti M, Giorgi I, Livi O, Scartoni V, Tiscione E. Biagi G, et al. Among authors: giorgi i. Farmaco. 1990 Nov;45(11):1181-92. Farmaco. 1990. PMID: 2128450

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