Di Giacomo B - Search Results

1

2-[N-Acylamino(C1-C3)alkyl]indoles as MT1 melatonin receptor partial agonists, antagonists, and putative inverse agonists.

Spadoni G, Balsamini C, Bedini A, Diamantini G, Di Giacomo B, Tontini A, Tarzia G, Mor M, Plazzi PV, Rivara S, Nonno R, Pannacci M, Lucini V, Fraschini F, Stankov BM. Spadoni G, et al. Among authors: di giacomo b. J Med Chem. 1998 Sep 10;41(19):3624-34. doi: 10.1021/jm970721h. J Med Chem. 1998. PMID: 9733487

2

Synthesis and conformational study of 3,4-carbocyclic bridged indole melatonin and serotonin analogues.

Bedini A, Di Giacomo B, Gatti G, Spadoni G. Bedini A, et al. Among authors: di giacomo b. Bioorg Med Chem. 2005 Aug 1;13(15):4651-7. doi: 10.1016/j.bmc.2005.04.064. Bioorg Med Chem. 2005. PMID: 15916895

3

Reassessing the melatonin pharmacophore--enantiomeric resolution, pharmacological activity, structure analysis, and molecular modeling of a constrained chiral melatonin analogue.

Rivara S, Diamantini G, Di Giacomo B, Lamba D, Gatti G, Lucini V, Pannacci M, Mor M, Spadoni G, Tarzia G. Rivara S, et al. Among authors: di giacomo b. Bioorg Med Chem. 2006 May 15;14(10):3383-91. doi: 10.1016/j.bmc.2005.12.053. Epub 2006 Jan 20. Bioorg Med Chem. 2006. PMID: 16431121

4

Synthesis and biological activity of new melatonin dimeric derivatives.

Di Giacomo B, Bedini A, Spadoni G, Tarzia G, Fraschini F, Pannacci M, Lucini V. Di Giacomo B, et al. Bioorg Med Chem. 2007 Jul 1;15(13):4643-50. doi: 10.1016/j.bmc.2007.03.080. Epub 2007 Mar 30. Bioorg Med Chem. 2007. PMID: 17481904

5

Conformationally restrained melatonin analogues: synthesis, binding affinity for the melatonin receptor, evaluation of the biological activity, and molecular modeling study.

Spadoni G, Balsamini C, Diamantini G, Di Giacomo B, Tarzia G, Mor M, Plazzi PV, Rivara S, Lucini V, Nonno R, Pannacci M, Fraschini F, Stankov BM. Spadoni G, et al. Among authors: di giacomo b. J Med Chem. 1997 Jun 20;40(13):1990-2002. doi: 10.1021/jm960651z. J Med Chem. 1997. PMID: 9207940

6

1-(2-Alkanamidoethyl)-6-methoxyindole derivatives: a new class of potent indole melatonin analogues.

Tarzia G, Diamantini G, Di Giacomo B, Spadoni G, Esposti D, Nonno R, Lucini V, Pannacci M, Fraschini F, Stankov BM. Tarzia G, et al. Among authors: di giacomo b. J Med Chem. 1997 Jun 20;40(13):2003-10. doi: 10.1021/jm960653j. J Med Chem. 1997. PMID: 9207941

7

Synthesis, pharmacological characterization and QSAR studies on 2-substituted indole melatonin receptor ligands.

Mor M, Spadoni G, Di Giacomo B, Diamantini G, Bedini A, Tarzia G, Plazzi PV, Rivara S, Nonno R, Lucini V, Pannacci M, Fraschini F, Stankov BM. Mor M, et al. Among authors: di giacomo b. Bioorg Med Chem. 2001 Apr;9(4):1045-57. doi: 10.1016/s0968-0896(00)00322-9. Bioorg Med Chem. 2001. PMID: 11354661

8

Synthesis and biological evaluation of 6-bromo-6-substituted penicillanic acid derivatives as beta-lactamase inhibitors.

Bedini A, Balsamini C, Di Giacomo B, Tontini A, Citterio B, Giorgi L, Di Modugno E, Tarzia G. Bedini A, et al. Among authors: di modugno e, di giacomo b. Farmaco. 2002 Aug;57(8):663-9. doi: 10.1016/s0014-827x(02)01261-2. Farmaco. 2002. PMID: 12361234

9

Synthesis of new C-6 alkyliden penicillin derivatives as beta-lactamase inhibitors.

Di Giacomo B, Tarzia G, Bedini A, Gatti G, Bartoccini F, Balsamini C, Tontini A, Baffone W, Di Modugno E, Felici A. Di Giacomo B, et al. Among authors: di modugno e. Farmaco. 2002 Apr;57(4):273-83. doi: 10.1016/s0014-827x(02)01207-7. Farmaco. 2002. PMID: 11989807

10

Pharmacological characterization of hydrolysis-resistant analogs of oleoylethanolamide with potent anorexiant properties.

Astarita G, Di Giacomo B, Gaetani S, Oveisi F, Compton TR, Rivara S, Tarzia G, Mor M, Piomelli D. Astarita G, et al. Among authors: di giacomo b. J Pharmacol Exp Ther. 2006 Aug;318(2):563-70. doi: 10.1124/jpet.106.105221. Epub 2006 May 15. J Pharmacol Exp Ther. 2006. PMID: 16702440

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