Colabufo NA - Search Results

1

Synthesis and toxicopharmacological evaluation of m-hydroxymexiletine, the first metabolite of mexiletine more potent than the parent compound on voltage-gated sodium channels.

Catalano A, Desaphy JF, Lentini G, Carocci A, Di Mola A, Bruno C, Carbonara R, De Palma A, Budriesi R, Ghelardini C, Perrone MG, Colabufo NA, Conte Camerino D, Franchini C. Catalano A, et al. Among authors: colabufo na. J Med Chem. 2012 Feb 9;55(3):1418-22. doi: 10.1021/jm201197z. Epub 2012 Jan 31. J Med Chem. 2012. PMID: 22191686

2

High affinity and selectivity on 5-HT1A receptor of 1-aryl-4-[1-tetralin)alkyl]piperazines. 2.

Perrone R, Berardi F, Colabufo NA, Leopoldo M, Tortorella V, Fiorentini F, Olgiati V, Ghiglieri A, Govoni S. Perrone R, et al. Among authors: colabufo na. J Med Chem. 1995 Mar 17;38(6):942-9. doi: 10.1021/jm00006a013. J Med Chem. 1995. PMID: 7699710

3

Mixed 5-HT1A/D-2 activity of a new model of arylpiperazines: 1-aryl-4-[3-(1,2-dihydronaphthalen-4-yl)-n-propyl]piperazines. 1. Synthesis and structure-activity relationships.

Perrone R, Berardi F, Colabufo NA, Tortorella V, Fiorentini F, Olgiati V, Vanotti E, Govoni S. Perrone R, et al. Among authors: colabufo na. J Med Chem. 1994 Jan 7;37(1):99-104. doi: 10.1021/jm00027a012. J Med Chem. 1994. PMID: 8289207

4

New sigma and 5-HT1A receptor ligands: omega-(tetralin-1-yl)-n-alkylamine derivatives.

Berardi F, Colabufo NA, Giudice G, Perrone R, Tortorella V, Govoni S, Lucchi L. Berardi F, et al. Among authors: colabufo na. J Med Chem. 1996 Jan 5;39(1):176-82. doi: 10.1021/jm950409c. J Med Chem. 1996. PMID: 8568804

5

N-[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide: a potent and selective dopamine D4 ligand.

Perrone R, Berardi F, Colabufo NA, Leopoldo M, Tortorella V. Perrone R, et al. Among authors: colabufo na. J Med Chem. 1998 Nov 19;41(24):4903-9. doi: 10.1021/jm981041x. J Med Chem. 1998. PMID: 9822559

6

1-aryl-4-[(5-methoxy-1,2,3, 4-tetrahydronaphthalen-1-yl)alkyl]piperazines and their analogues: influence of the stereochemistry of the tetrahydronaphthalen-1-yl nucleus on 5-HT1A receptor affinity and selectivity versus alpha1 and D2 receptors. 5.

Perrone R, Berardi F, Colabufo NA, Leopoldo M, Tortorella V. Perrone R, et al. Among authors: colabufo na. J Med Chem. 1999 Feb 11;42(3):490-6. doi: 10.1021/jm980420n. J Med Chem. 1999. PMID: 9986719

7

A multireceptorial binding reinvestigation on an extended class of sigma ligands: N-[omega-(indan-1-yl and tetralin-1-yl)alkyl] derivatives of 3,3-dimethylpiperidine reveal high affinities towards sigma1 and EBP sites.

Berardi F, Ferorelli S, Colabufo NA, Leopoldo M, Perrone R, Tortorella V. Berardi F, et al. Among authors: colabufo na. Bioorg Med Chem. 2001 May;9(5):1325-35. doi: 10.1016/s0968-0896(01)00011-6. Bioorg Med Chem. 2001. PMID: 11377189

8

trans-4-[4-(Methoxyphenyl)cyclohexyl]-1-arylpiperazines: a new class of potent and selective 5-HT(1A) receptor ligands as conformationally constrained analogues of 4-[3-(5-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)propyl]-1-arylpiperazines.

Perrone R, Berardi F, Colabufo NA, Leopoldo M, Lacivita E, Tortorella V, Leonardi A, Poggesi E, Testa R. Perrone R, et al. Among authors: colabufo na. J Med Chem. 2001 Dec 6;44(25):4431-42. doi: 10.1021/jm010866v. J Med Chem. 2001. PMID: 11728188

9

Structure-affinity relationship study on N-[4-(4-arylpiperazin-1-yl)butyl]arylcarboxamides as potent and selective dopamine D(3) receptor ligands.

Leopoldo M, Berardi F, Colabufo NA, De Giorgio P, Lacivita E, Perrone R, Tortorella V. Leopoldo M, et al. Among authors: colabufo na. J Med Chem. 2002 Dec 19;45(26):5727-35. doi: 10.1021/jm020952a. J Med Chem. 2002. PMID: 12477356

10

Synthesis and structure-affinity relationships of 1-[omega-(4-aryl-1-piperazinyl)alkyl]-1-aryl ketones as 5-HT(7) receptor ligands.

Perrone R, Berardi F, Colabufo NA, Lacivita E, Leopoldo M, Tortorella V. Perrone R, et al. Among authors: colabufo na. J Med Chem. 2003 Feb 13;46(4):646-9. doi: 10.1021/jm020994z. J Med Chem. 2003. PMID: 12570387

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