Macchia M - Search Results

1

CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators.

Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G. Gado F, et al. Among authors: macchia m. Eur J Pharm Sci. 2022 Feb 1;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 1. Eur J Pharm Sci. 2022. PMID: 34863873 Free article.

2

Conformationally restrained analogs of sympathomimetic catecholamines. Synthesis, conformational analysis, and adrenergic activity of isochroman derivatives.

Macchia B, Balsamo A, Breschi MC, Chiellini G, Lapucci A, Macchia M, Manera C, Martinelli A, Martini C, Scatizzi R, et al. Macchia B, et al. Among authors: macchia m. J Med Chem. 1993 Oct 15;36(21):3077-86. doi: 10.1021/jm00073a006. J Med Chem. 1993. PMID: 8230093

3

(E)-(arylmethyleneaminoxy)acetamides as analogues of neuroleptic benzamides: synthesis and D2-dopaminergic binding affinity.

Macchia M, Manera C, Martinelli A, Orlandini E, Romagnoli F, Rossello A, Chiellini G. Macchia M, et al. Farmaco. 1995 Oct;50(10):719-24. Farmaco. 1995. PMID: 8590580

4

Synthesis and antimicrobial activity of benzo[a]dihydrocarbazole and benzotetrahydrocyclohept[1,2-b]indole derivatives.

Macchia M, Manera C, Nencetti S, Rossello A, Broccali G, Limonta D. Macchia M, et al. Farmaco. 1996 Jan;51(1):75-8. Farmaco. 1996. PMID: 8721766

5

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. Among authors: macchia m. J Med Chem. 2001 Nov 22;44(24):4288-91. doi: 10.1021/jm010948j. J Med Chem. 2001. PMID: 11708930

6

Synthesis, antifungal activity, and molecular modeling studies of new inverted oxime ethers of oxiconazole.

Rossello A, Bertini S, Lapucci A, Macchia M, Martinelli A, Rapposelli S, Herreros E, Macchia B. Rossello A, et al. Among authors: macchia m, macchia b. J Med Chem. 2002 Oct 24;45(22):4903-12. doi: 10.1021/jm020980t. J Med Chem. 2002. PMID: 12383016

7

4-[6-(Dansylamino)hexylamino]-7-methyl-2-phenyl-1,8-naphthyridine as a new potential fluorescent probe for studying A1-adenosine receptor.

Macchia M, Bertini S, Di Bussolo V, Manera C, Martini C, Minutolo F, Mori C, Saccomanni G, Tuscano D, Ferrarini PL. Macchia M, et al. Farmaco. 2002 Oct;57(10):783-6. doi: 10.1016/s0014-827x(02)01275-2. Farmaco. 2002. PMID: 12420873

8

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: macchia b. J Med Chem. 2003 Jan 2;46(1):161-8. doi: 10.1021/jm021019a. J Med Chem. 2003. PMID: 12502370

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. 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. Among authors: macchia m. 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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