Minutolo F - Search Results

1

Reversible Monoacylglycerol Lipase Inhibitors: Discovery of a New Class of Benzylpiperidine Derivatives.

Bononi G, Di Stefano M, Poli G, Ortore G, Meier P, Masetto F, Caligiuri I, Rizzolio F, Macchia M, Chicca A, Avan A, Giovannetti E, Vagaggini C, Brai A, Dreassi E, Valoti M, Minutolo F, Granchi C, Gertsch J, Tuccinardi T. Bononi G, et al. Among authors: minutolo f. J Med Chem. 2022 May 26;65(10):7118-7140. doi: 10.1021/acs.jmedchem.1c01806. Epub 2022 May 6. J Med Chem. 2022. PMID: 35522977 Free PMC article.

2

Synthesis and dopaminergic properties of the two enantiomers of 3-(3,4-dimethylphenyl)-1-propylpiperidine, a potent and selective dopamine D4 receptor ligand.

Macchia B, Cervetto L, Demontis GC, Domiano P, Longoni B, Macchia M, Minutolo F, Orlandini E, Ortore G, Papi C. Macchia B, et al. Among authors: minutolo f. Bioorg Med Chem Lett. 2001 Jan 22;11(2):223-6. doi: 10.1016/s0960-894x(00)00633-8. Bioorg Med Chem Lett. 2001. PMID: 11206464

3

Design, synthesis, and characterization of the antitumor activity of novel ceramide analogues.

Macchia M, Barontini S, Bertini S, Di Bussolo V, Fogli S, Giovannetti E, Grossi E, Minutolo F, Danesi R. Macchia M, et al. Among authors: minutolo f. J Med Chem. 2001 Nov 8;44(23):3994-4000. doi: 10.1021/jm010947r. J Med Chem. 2001. PMID: 11689086

4

Salicylaldoxime moiety as a phenolic "A-Ring" substitute in estrogen receptor ligands.

Minutolo F, Bertini S, Papi C, Carlson KE, Katzenellenbogen JA, Macchia M. Minutolo F, et al. J Med Chem. 2001 Nov 22;44(24):4288-91. doi: 10.1021/jm010948j. J Med Chem. 2001. PMID: 11708930

5

7-Nitrobenzofurazan (NBD) derivatives of 5'-N-ethylcarboxamidoadenosine (NECA) as new fluorescent probes for human A(3) adenosine receptors.

Macchia M, Salvetti F, Bertini S, Di Bussolo V, Gattuso L, Gesi M, Hamdan M, Klotz KN, Laragione T, Lucacchini A, Minutolo F, Nencetti S, Papi C, Tuscano D, Martini C. Macchia M, et al. Among authors: minutolo f. Bioorg Med Chem Lett. 2001 Dec 3;11(23):3023-6. doi: 10.1016/s0960-894x(01)00610-2. Bioorg Med Chem Lett. 2001. PMID: 11714602

6

Aryl-substituted methyleneaminoxymethyl (MAOM) analogues of diarylcyclopentenyl cyclooxygenase-2 inhibitors: effects of some structural modifications on their biological properties.

Balsamo A, Coletta I, Guglielmotti A, Landolfi C, Lapucci A, Mancini F, Milanese C, Minutolo F, Orlandini E, Ortore G, Pinza M, Rapposelli S. Balsamo A, et al. Among authors: minutolo f. Eur J Med Chem. 2002 Jul;37(7):585-94. doi: 10.1016/s0223-5234(02)01385-5. Eur J Med Chem. 2002. PMID: 12126777

7

New N-n-propyl-substituted 3-aryl- and 3-cyclohexylpiperidines as partial agonists at the D4 dopamine receptor.

Macchia M, Cervetto L, Demontis GC, Longoni B, Minutolo F, Orlandini E, Ortore G, Papi C, Sbrana A, Macchia B. Macchia M, et al. Among authors: minutolo f. J Med Chem. 2003 Jan 2;46(1):161-8. doi: 10.1021/jm021019a. J Med Chem. 2003. PMID: 12502370

8

Conformationally restrained ceramide analogues: effects of lipophilic modifications on the antiproliferative activity.

Macchia M, Antonello M, Bertini S, Di Bussolo V, Fogli S, Giovannetti E, Minutolo F, Rapposelli S, Danesi R. Macchia M, et al. Among authors: minutolo f. Farmaco. 2003 Jan;58(1):85-9. doi: 10.1016/S0014-827X(02)00002-2. Farmaco. 2003. PMID: 12595041

9

Ceramide analogues in apoptosis: a new strategy for anticancer drug development.

Macchia M, Bertini S, Fogli S, Giovannetti E, Minutolo F, Rapposelli S, Danesi R. Macchia M, et al. Among authors: minutolo f. Farmaco. 2003 Mar;58(3):205-11. doi: 10.1016/S0014-827X(03)00015-6. Farmaco. 2003. PMID: 12620416 Review.

10

Synthesis, binding affinity, and transcriptional activity of hydroxy- and methoxy-substituted 3,4-diarylsalicylaldoximes on estrogen receptors alpha and beta.

Minutolo F, Antonello M, Bertini S, Rapposelli S, Rossello A, Sheng S, Carlson KE, Katzenellenbogen JA, Macchia M. Minutolo F, et al. Bioorg Med Chem. 2003 Apr 3;11(7):1247-57. doi: 10.1016/s0968-0896(02)00640-5. Bioorg Med Chem. 2003. PMID: 12628652

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