Rivara S - Search Results

1

Novel Symmetrical Benzazolyl Derivatives Endowed with Potent Anti-Heparanase Activity.

Messore A, Madia VN, Pescatori L, Saccoliti F, Tudino V, De Leo A, Bortolami M, De Vita D, Scipione L, Pepi F, Costi R, Rivara S, Scalvini L, Mor M, Ferrara FF, Pavoni E, Roscilli G, Cassinelli G, Milazzo FM, Battistuzzi G, Di Santo R, Giannini G. Messore A, et al. Among authors: rivara s. J Med Chem. 2018 Dec 13;61(23):10834-10859. doi: 10.1021/acs.jmedchem.8b01497. Epub 2018 Nov 29. J Med Chem. 2018. PMID: 30412404 Free article.

2

An Optimized Workflow for the Discovery of New Antimicrobial Compounds Targeting Bacterial RNA Polymerase Complex Formation.

Caputo A, Sartini S, Levati E, Minato I, Elisi GM, Di Stasi A, Guillou C, Goekjian PG, Garcia P, Gueyrard D, Bach S, Comte A, Ottonello S, Rivara S, Montanini B. Caputo A, et al. Among authors: rivara s. Antibiotics (Basel). 2022 Oct 21;11(10):1449. doi: 10.3390/antibiotics11101449. Antibiotics (Basel). 2022. PMID: 36290107 Free PMC article.

3

Three-dimensional quantitative structure-activity relationship studies on selected MT1 and MT2 melatonin receptor ligands: requirements for subtype selectivity and intrinsic activity modulation.

Rivara S, Mor M, Silva C, Zuliani V, Vacondio F, Spadoni G, Bedini A, Tarzia G, Lucini V, Pannacci M, Fraschini F, Plazzi PV. Rivara S, et al. J Med Chem. 2003 Apr 10;46(8):1429-39. doi: 10.1021/jm020982d. J Med Chem. 2003. PMID: 12672242

4

Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors.

Tarzia G, Duranti A, Tontini A, Piersanti G, Mor M, Rivara S, Plazzi PV, Park C, Kathuria S, Piomelli D. Tarzia G, et al. Among authors: rivara s. J Med Chem. 2003 Jun 5;46(12):2352-60. doi: 10.1021/jm021119g. J Med Chem. 2003. PMID: 12773040 Free article.

5

Synthesis and structure-activity relationships of a series of pyrrole cannabinoid receptor agonists.

Tarzia G, Duranti A, Tontini A, Spadoni G, Mor M, Rivara S, Vincenzo Plazzi P, Kathuria S, Piomelli D. Tarzia G, et al. Among authors: rivara s. Bioorg Med Chem. 2003 Sep 1;11(18):3965-73. doi: 10.1016/s0968-0896(03)00413-9. Bioorg Med Chem. 2003. PMID: 12927857

6

Synthesis and three-dimensional quantitative structure-activity relationship analysis of H3 receptor antagonists containing a neutral heterocyclic polar group.

Rivara S, Mor M, Bordi F, Silva C, Zuliani V, Vacondio F, Morini G, Plazzi PV, Carrupt PA, Testa B. Rivara S, et al. Drug Des Discov. 2003;18(2-3):65-79. Drug Des Discov. 2003. PMID: 14675944

7

Synthesis, biological activity, QSAR and QSPR study of 2-aminobenzimidazole derivatives as potent H3-antagonists.

Mor M, Bordi F, Silva C, Rivara S, Zuliani V, Vacondio F, Rivara M, Barocelli E, Bertoni S, Ballabeni V, Magnanini F, Impicciatore M, Plazzi PV. Mor M, et al. Among authors: rivara m, rivara s. Bioorg Med Chem. 2004 Feb 15;12(4):663-74. doi: 10.1016/j.bmc.2003.11.030. Bioorg Med Chem. 2004. PMID: 14759727

8

Strategies leading to MT2 selective melatonin receptor antagonists.

Spadoni G, Bedini A, Piersanti G, Mor M, Rivara S, Tarzia G. Spadoni G, et al. Among authors: rivara s. Adv Exp Med Biol. 2003;527:577-85. doi: 10.1007/978-1-4615-0135-0_66. Adv Exp Med Biol. 2003. PMID: 15206776

9

Synthesis, pharmacological evaluation, and structure-activity relationships of benzopyran derivatives with potent SERM activity.

Amari G, Armani E, Ghirardi S, Delcanale M, Civelli M, Caruso PL, Galbiati E, Lipreri M, Rivara S, Lodola A, Mor M. Amari G, et al. Among authors: rivara s. Bioorg Med Chem. 2004 Jul 15;12(14):3763-82. doi: 10.1016/j.bmc.2004.05.015. Bioorg Med Chem. 2004. PMID: 15210143

10

Imidazole H3-antagonists: relationship between structure and ex vivo binding to rat brain H3-receptors.

Vacondio F, Mor M, Silva C, Zuliani V, Rivara M, Rivara S, Bordi F, Plazzi PV, Magnanini F, Bertoni S, Ballabeni V, Barocelli E, Carrupt PA, Testa B. Vacondio F, et al. Among authors: rivara m, rivara s. Eur J Pharm Sci. 2004 Sep;23(1):89-98. doi: 10.1016/j.ejps.2004.06.003. Eur J Pharm Sci. 2004. PMID: 15324926

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