Cerri A - Search Results

1

Replacement of the quinoline system in 2-phenyl-4-quinolinecarboxamide NK-3 receptor antagonists.

Giardina GA, Artico M, Cavagnera S, Cerri A, Consolandi E, Gagliardi S, Graziani D, Grugni M, Hay DW, Luttmann MA, Mena R, Raveglia LF, Rigolio R, Sarau HM, Schmidt DB, Zanoni G, Farina C. Giardina GA, et al. Among authors: cerri a. Farmaco. 1999 Jun 30;54(6):364-74. doi: 10.1016/s0014-827x(99)00043-9. Farmaco. 1999. PMID: 10443017

2

Synthesis and nootropic activity of 2-oxo-1-pyrrolidinesulfonic acid derivatives.

Cerri A, Farina C, Pinza M, Banfi S. Cerri A, et al. Farmaco. 1991 Jul-Aug;46(7-8):959-66. Farmaco. 1991. PMID: 1793478

3

Synthesis and NMR characterization of a novel class of thienomorphinans.

Ronzoni S, Cerri A, Dondio G, Fronza G, Petrillo P, Raveglia LF, Gatti PA. Ronzoni S, et al. Among authors: cerri a. Org Lett. 1999 Aug 12;1(3):513-5. doi: 10.1021/ol990693s. Org Lett. 1999. PMID: 10822591

4

Discovery of diaryl imidazolidin-2-one derivatives, a novel class of muscarinic M3 selective antagonists (Part 2).

Peretto I, Fossati C, Giardina GA, Giardini A, Guala M, La Porta E, Petrillo P, Radaelli S, Radice L, Raveglia LF, Santoro E, Scudellaro R, Scarpitta F, Cerri A, Menegon S, Dondio GM, Rizzi A, Armani E, Amari G, Civelli M, Villetti G, Patacchini R, Bergamaschi M, Bassani F, Delcanale M, Imbimbo BP. Peretto I, et al. Among authors: cerri a. J Med Chem. 2007 Apr 5;50(7):1693-7. doi: 10.1021/jm061160+. Epub 2007 Mar 13. J Med Chem. 2007. PMID: 17352463

5

Selective Oxidation of Hydroxy Groups of Bafilomycin A(1).

Gatti PA, Gagliardi S, Cerri A, Visconti M, Farina C. Gatti PA, et al. Among authors: cerri a. J Org Chem. 1996 Oct 4;61(20):7185-7188. doi: 10.1021/jo9607222. J Org Chem. 1996. PMID: 11667625 No abstract available.

6

Synthesis and pharmacological activity of a series of dihydro-1H-pyrrolo[1,2-a]imidazole-2,5(3H,6H)-diones, a novel class of potent cognition enhancers.

Pinza M, Farina C, Cerri A, Pfeiffer U, Riccaboni MT, Banfi S, Biagetti R, Pozzi O, Magnani M, Dorigotti L. Pinza M, et al. Among authors: cerri a. J Med Chem. 1993 Dec 24;36(26):4214-20. doi: 10.1021/jm00078a011. J Med Chem. 1993. PMID: 8277504

7

17 alpha-O-(aminoalkyl)oxime derivatives of 3 beta,14 beta-dihydroxy-5 beta-androstane and 3 beta-hydroxy-14-oxoseco-D-5 beta-androstane as inhibitors of Na(+),K(+)-ATPase at the digitalis receptor.

Gobbini M, Barassi P, Cerri A, De Munari S, Fedrizzi G, Santagostino M, Schiavone A, Torri M, Melloni P. Gobbini M, et al. Among authors: cerri a. J Med Chem. 2001 Nov 8;44(23):3821-30. doi: 10.1021/jm0109208. J Med Chem. 2001. PMID: 11689068

8

Structure-based design and synthesis of novel potent Na+,K+ -ATPase inhibitors derived from a 5alpha,14alpha-androstane scaffold as positive inotropic compounds.

De Munari S, Cerri A, Gobbini M, Almirante N, Banfi L, Carzana G, Ferrari P, Marazzi G, Micheletti R, Schiavone A, Sputore S, Torri M, Zappavigna MP, Melloni P. De Munari S, et al. Among authors: cerri a. J Med Chem. 2003 Aug 14;46(17):3644-54. doi: 10.1021/jm030830y. J Med Chem. 2003. PMID: 12904068

9

Synthesis and inotropic activity of 1-(O-aminoalkyloximes) of perhydroindene derivatives as simplified digitalis-like compounds acting on the Na(+),K(+)-ATPase.

Cerri A, Almirante N, Barassi P, Benicchio A, De Munari S, Marazzi G, Molinari I, Serra F, Melloni P. Cerri A, et al. J Med Chem. 2002 Jan 3;45(1):189-207. doi: 10.1021/jm011001k. J Med Chem. 2002. PMID: 11754591

10

Synthesis, cardiotonic activity, and structure-activity relationships of 17 beta-guanylhydrazone derivatives of 5 beta-androstane-3 beta, 14 beta-diol acting on the Na+,K(+)-ATPase receptor.

Cerri A, Serra F, Ferrari P, Folpini E, Padoani G, Melloni P. Cerri A, et al. J Med Chem. 1997 Oct 10;40(21):3484-8. doi: 10.1021/jm970312l. J Med Chem. 1997. PMID: 9341924

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