Nacci V - Search Results

1

A concerted study using binding measurements, X-ray structural data, and molecular modeling on the stereochemical features responsible for the affinity of 6-arylpyrrolo[2,1-d][1,5]benzothiazepines toward mitochondrial benzodiazepine receptors.

Dalpiaz A, Bertolasi V, Borea PA, Nacci V, Fiorini I, Campiani G, Mennini T, Manzoni C, Novellino E, Greco G. Dalpiaz A, et al. Among authors: nacci v. J Med Chem. 1995 Nov 10;38(23):4730-8. doi: 10.1021/jm00023a013. J Med Chem. 1995. PMID: 7473601

2

Pyrrolo[1,3]benzothiazepine-based atypical antipsychotic agents. Synthesis, structure-activity relationship, molecular modeling, and biological studies.

Campiani G, Butini S, Gemma S, Nacci V, Fattorusso C, Catalanotti B, Giorgi G, Cagnotto A, Goegan M, Mennini T, Minetti P, Di Cesare MA, Mastroianni D, Scafetta N, Galletti B, Stasi MA, Castorina M, Pacifici L, Ghirardi O, Tinti O, Carminati P. Campiani G, et al. Among authors: nacci v. J Med Chem. 2002 Jan 17;45(2):344-59. doi: 10.1021/jm010982y. J Med Chem. 2002. PMID: 11784139

3

Synthesis of new molecular probes for investigation of steroid biosynthesis induced by selective interaction with peripheral type benzodiazepine receptors (PBR).

Campiani G, Ramunno A, Fiorini I, Nacci V, Morelli E, Novellino E, Goegan M, Mennini T, Sullivan S, Zisterer DM, Williams CD. Campiani G, et al. Among authors: nacci v. J Med Chem. 2002 Sep 12;45(19):4276-81. doi: 10.1021/jm020849l. J Med Chem. 2002. PMID: 12213069

4

Pyrrolo[2,1-c][1,4]benzothiazines: synthesis, structure-activity relationships, molecular modeling studies, and cardiovascular activity.

Campiani G, Garofalo A, Fiorini I, Botta M, Nacci V, Tafi A, Chiarini A, Budriesi R, Bruni G, Romeo MR. Campiani G, et al. Among authors: nacci v. J Med Chem. 1995 Oct 27;38(22):4393-410. doi: 10.1021/jm00022a005. J Med Chem. 1995. PMID: 7473567

5

A comparative molecular field analysis model for 6-arylpyrrolo[2,1-d] [1,5]benzothiazepines binding selectively to the mitochondrial benzodiazepine receptor.

Greco G, Novellino E, Fiorini I, Nacci V, Campiani G, Ciani SM, Garofalo A, Bernasconi P, Mennini T. Greco G, et al. Among authors: nacci v. J Med Chem. 1994 Nov 25;37(24):4100-8. doi: 10.1021/jm00050a007. J Med Chem. 1994. PMID: 7990110

6

Novel ligands specific for mitochondrial benzodiazepine receptors: 6-arylpyrrolo[2,1-d][1,5]benzothiazepine derivatives. Synthesis, structure-activity relationships, and molecular modeling studies.

Fiorini I, Nacci V, Ciani SM, Garofalo A, Campiani G, Savini L, Novellino E, Greco G, Bernasconi P, Mennini T. Fiorini I, et al. Among authors: nacci v. J Med Chem. 1994 May 13;37(10):1427-38. doi: 10.1021/jm00036a007. J Med Chem. 1994. PMID: 8182701

7

Pyrrolobenzothiazepinones and pyrrolobenzoxazepinones: novel and specific non-nucleoside HIV-1 reverse transcriptase inhibitors with antiviral activity.

Campiani G, Nacci V, Fiorini I, De Filippis MP, Garofalo A, Greco G, Novellino E, Altamura S, Di Renzo L. Campiani G, et al. Among authors: nacci v. J Med Chem. 1996 Jul 5;39(14):2672-80. doi: 10.1021/jm950702c. J Med Chem. 1996. PMID: 8709096

8

Cardiovascular characterization of pyrrolo[2,1-d][1,5]benzothiazepine derivatives binding selectively to the peripheral-type benzodiazepine receptor (PBR): from dual PBR affinity and calcium antagonist activity to novel and selective calcium entry blockers.

Campiani G, Fiorini I, De Filippis MP, Ciani SM, Garofalo A, Nacci V, Giorgi G, Sega A, Botta M, Chiarini A, Budriesi R, Bruni G, Romeo MR, Manzoni C, Mennini T. Campiani G, et al. Among authors: nacci v. J Med Chem. 1996 Jul 19;39(15):2922-38. doi: 10.1021/jm960162z. J Med Chem. 1996. PMID: 8709127

9

Synthesis, biological activity, and SARs of pyrrolobenzoxazepine derivatives, a new class of specific "peripheral-type" benzodiazepine receptor ligands.

Campiani G, Nacci V, Fiorini I, De Filippis MP, Garofalo A, Ciani SM, Greco G, Novellino E, Williams DC, Zisterer DM, Woods MJ, Mihai C, Manzoni C, Mennini T. Campiani G, et al. Among authors: nacci v. J Med Chem. 1996 Aug 30;39(18):3435-50. doi: 10.1021/jm960251b. J Med Chem. 1996. PMID: 8784441

10

Diltiazem-like calcium entry blockers: a hypothesis of the receptor-binding site based on a comparative molecular field analysis model.

Corelli F, Manetti F, Tafi A, Campiani G, Nacci V, Botta M. Corelli F, et al. Among authors: nacci v. J Med Chem. 1997 Jan 3;40(1):125-31. doi: 10.1021/jm9605647. J Med Chem. 1997. PMID: 9016337

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