Rivara S - Search Results

1

UniPR129 is a competitive small molecule Eph-ephrin antagonist blocking in vitro angiogenesis at low micromolar concentrations.

Hassan-Mohamed I, Giorgio C, Incerti M, Russo S, Pala D, Pasquale EB, Zanotti I, Vicini P, Barocelli E, Rivara S, Mor M, Lodola A, Tognolini M. Hassan-Mohamed I, et al. Among authors: rivara s. Br J Pharmacol. 2014 Dec;171(23):5195-208. doi: 10.1111/bph.12669. Epub 2014 Aug 28. Br J Pharmacol. 2014. PMID: 24597515 Free PMC article.

2

In vitro characterization of potency, affinity and selectivity of H3-antagonists: from thioperamide to thioperamide unrelated imidazole derivatives.

Barocelli E, Ballabeni V, Caretta A, Bertoni S, Bordi F, Rivara S, Silva C, Mor M, Impicciatore M. Barocelli E, et al. Among authors: rivara s. Farmaco. 1997 Jun-Jul;52(6-7):463-9. Farmaco. 1997. PMID: 9372599

3

Plasma concentration and brain penetration of the H3-receptor antagonist thioperamide in rats.

Silva C, Mor M, Bordi F, Rivara S, Caretta A, Ballabeni V, Barocelli E, Plazzi PV. Silva C, et al. Among authors: rivara s. Farmaco. 1997 Jun-Jul;52(6-7):457-62. Farmaco. 1997. PMID: 9372598

4

Epidermal growth factor receptor irreversible inhibitors: chemical exploration of the cysteine-trap portion.

Carmi C, Lodola A, Rivara S, Vacondio F, Cavazzoni A, Alfieri RR, Ardizzoni A, Petronini PG, Mor M. Carmi C, et al. Among authors: rivara s. Mini Rev Med Chem. 2011 Oct;11(12):1019-30. doi: 10.2174/138955711797247725. Mini Rev Med Chem. 2011. PMID: 21861809 Review.

5

Synthesis and biological assays of new H3-antagonists with imidazole and imidazoline polar groups.

Mor M, Bordi F, Silva C, Rivara S, Zuliani V, Vacondio F, Morini G, Barocelli E, Ballabeni V, Impicciatore M, Plazzi PV. Mor M, et al. Among authors: rivara s. Farmaco. 2000 Jan;55(1):27-34. doi: 10.1016/s0014-827x(99)00115-9. Farmaco. 2000. PMID: 10755228

6

H3-receptor antagonists: synthesis and structure-activity relationships of para- and meta-substituted 4(5)-phenyl-2-[[2-[4(5)-imidazolyl]ethyl]thio]imidazoles.

Mor M, Bordi F, Silva C, Rivara S, Crivori P, Plazzi PV, Ballabeni V, Caretta A, Barocelli E, Impicciatore M, Carrupt PA, Testa B. Mor M, et al. Among authors: rivara s. J Med Chem. 1997 Aug 1;40(16):2571-8. doi: 10.1021/jm970070p. J Med Chem. 1997. PMID: 9258364

7

Structure-property relationships on histamine H3-antagonists: binding of phenyl-substituted alkylthioimidazole derivatives to rat plasma proteins.

Silva C, Plazzi PV, Bordi F, Rivara S, Vacondio F, Zuliani V, Caretta A, Mor M. Silva C, et al. Among authors: rivara s. Farmaco. 2000 Apr;55(4):239-45. doi: 10.1016/s0014-827x(00)00026-4. Farmaco. 2000. PMID: 10966153

8

Ligands of the histamine H3-receptor: new potent antagonists of the 2-thioimidazole type.

Plazzi PV, Mor M, Bordi F, Silva C, Rivara S, Caretta A, Ballabeni V, Impicciatore M, Vitali T. Plazzi PV, et al. Among authors: rivara s. Farmaco. 1997 May;52(5):295-302. Farmaco. 1997. PMID: 9274000

9

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: rivara s. Bioorg Med Chem. 2001 Apr;9(4):1045-57. doi: 10.1016/s0968-0896(00)00322-9. Bioorg Med Chem. 2001. PMID: 11354661

10

2-N-acylaminoalkylindoles: design and quantitative structure-activity relationship studies leading to MT2-selective melatonin antagonists.

Spadoni G, Balsamini C, Diamantini G, Tontini A, Tarzia G, Mor M, Rivara S, Plazzi PV, Nonno R, Lucini V, Pannacci M, Fraschini F, Stankov BM. Spadoni G, et al. Among authors: rivara s. J Med Chem. 2001 Aug 30;44(18):2900-12. doi: 10.1021/jm001125h. J Med Chem. 2001. PMID: 11520198

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