Poggesi E - Search Results

1

New potential uroselective NO-donor alpha1-antagonists.

Boschi D, Tron GC, Di Stilo A, Fruttero R, Gasco A, Poggesi E, Motta G, Leonardi A. Boschi D, et al. Among authors: poggesi e. J Med Chem. 2003 Aug 14;46(17):3762-5. doi: 10.1021/jm030825u. J Med Chem. 2003. PMID: 12904082

2

1,3-dioxolane-based ligands as a novel class of alpha1-adrenoceptor antagonists.

Brasili L, Sorbi C, Franchini S, Manicardi M, Angeli P, Marucci G, Leonardi A, Poggesi E. Brasili L, et al. Among authors: poggesi e. J Med Chem. 2003 Apr 10;46(8):1504-11. doi: 10.1021/jm021078o. J Med Chem. 2003. PMID: 12672251

3

Synthesis, screening, and molecular modeling of new potent and selective antagonists at the alpha 1d adrenergic receptor.

Leonardi A, Barlocco D, Montesano F, Cignarella G, Motta G, Testa R, Poggesi E, Seeber M, De Benedetti PG, Fanelli F. Leonardi A, et al. Among authors: poggesi e. J Med Chem. 2004 Apr 8;47(8):1900-18. doi: 10.1021/jm030944+. J Med Chem. 2004. PMID: 15055991

4

1,2,4-Benzothiadiazine derivatives as alpha1 and 5-HT1A receptor ligands.

Tait A, Luppi A, Franchini S, Preziosi E, Parenti C, Buccioni M, Marucci G, Leonardi A, Poggesi E, Brasili L. Tait A, et al. Among authors: poggesi e. Bioorg Med Chem Lett. 2005 Feb 15;15(4):1185-8. doi: 10.1016/j.bmcl.2004.12.004. Bioorg Med Chem Lett. 2005. PMID: 15686938

5

Design, synthesis, and biological activity of prazosin-related antagonists. Role of the piperazine and furan units of prazosin on the selectivity for alpha1-adrenoreceptor subtypes.

Bolognesi ML, Budriesi R, Chiarini A, Poggesi E, Leonardi A, Melchiorre C. Bolognesi ML, et al. Among authors: poggesi e. J Med Chem. 1998 Nov 19;41(24):4844-53. doi: 10.1021/jm9810654. J Med Chem. 1998. PMID: 9822553

6

Structure-activity relationships in 1,4-benzodioxan-related compounds. 7. Selectivity of 4-phenylchroman analogues for alpha(1)-adrenoreceptor subtypes.

Quaglia W, Pigini M, Piergentili A, Giannella M, Gentili F, Marucci G, Carrieri A, Carotti A, Poggesi E, Leonardi A, Melchiorre C. Quaglia W, et al. Among authors: poggesi e. J Med Chem. 2002 Apr 11;45(8):1633-43. doi: 10.1021/jm011066n. J Med Chem. 2002. PMID: 11931617

7

Rosini M, Antonello A, Cavalli A, Bolognesi ML, Minarini A, Marucci G, Poggesi E, Leonardi A, Melchiorre C. Rosini M, et al. Among authors: poggesi e. J Med Chem. 2003 Nov 6;46(23):4895-903. doi: 10.1021/jm030952q. J Med Chem. 2003. PMID: 14584940

8

Synthesis and structure-activity relationships of 1-aralkyl-4-benzylpiperidine and 1-aralkyl-4-benzylpiperazine derivatives as potent sigma ligands.

Costantino L, Gandolfi F, Sorbi C, Franchini S, Prezzavento O, Vittorio F, Ronsisvalle G, Leonardi A, Poggesi E, Brasili L. Costantino L, et al. Among authors: poggesi e. J Med Chem. 2005 Jan 13;48(1):266-73. doi: 10.1021/jm049433t. J Med Chem. 2005. PMID: 15634021

9

Structure-activity relationships in 1,4-benzodioxan-related compounds. 8.(1) {2-[2-(4-chlorobenzyloxy)phenoxy]ethyl}-[2-(2,6-dimethoxyphenoxy)ethyl]amine (clopenphendioxan) as a tool to highlight the involvement of alpha1D- and alpha1B-adrenoreceptor subtypes in the regulation of human PC-3 prostate cancer cell apoptosis and proliferation.

Quaglia W, Santoni G, Pigini M, Piergentili A, Gentili F, Buccioni M, Mosca M, Lucciarini R, Amantini C, Nabissi MI, Ballarini P, Poggesi E, Leonardi A, Giannella M. Quaglia W, et al. Among authors: poggesi e. J Med Chem. 2005 Dec 1;48(24):7750-63. doi: 10.1021/jm0580398. J Med Chem. 2005. PMID: 16302814

10

Synthesis and alpha(1)-adrenoceptor antagonist activity of derivatives and isosters of the furan portion of (+)-cyclazosin.

Sagratini G, Angeli P, Buccioni M, Gulini U, Marucci G, Melchiorre C, Leonardi A, Poggesi E, Giardinà D. Sagratini G, et al. Among authors: poggesi e. Bioorg Med Chem. 2007 Mar 15;15(6):2334-45. doi: 10.1016/j.bmc.2007.01.028. Epub 2007 Jan 19. Bioorg Med Chem. 2007. PMID: 17276073

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