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Roberto Perrone

Dipartimento Farmaco-Chimico

Universitá di Bari

via Orabona

4, 70126 Bari

Italy

[email]@*.uniba.it

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Dipartimento Farmaco-Chimico, Universitá di Bari, via Orabona, 4, 70126 Bari, Italy. 2000 - 2005

References

  1. Design and synthesis of long-chain arylpiperazines with mixed affinity for serotonin transporter (SERT) and 5-HT(1A) receptor. Perrone, R., Berardi, F., Colabufo, N.A., Lacivita, E., Larizza, C., Leopoldo, M., Tortorella, V. J. Pharm. Pharmacol. (2005) [Pubmed]
  2. 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, N.A., Lacivita, E., Leopoldo, M., Tortorella, V. J. Med. Chem. (2003) [Pubmed]
  3. 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, N.A., Leopoldo, M., Lacivita, E., Tortorella, V., Leonardi, A., Poggesi, E., Testa, R. J. Med. Chem. (2001) [Pubmed]
  4. A structure-affinity relationship study on derivatives of N-[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide, a high-affinity and selective D(4) receptor ligand. Perrone, R., Berardi, F., Colabufo, N.A., Leopoldo, M., Tortorella, V. J. Med. Chem. (2000) [Pubmed]
  5. 1-Substituted-4-[3-(1,2,3,4-tetrahydro-5- or 7-methoxynaphthalen-1-yl)propyl]piperazines: influence of the N-1 piperazine substituent on 5-HT1A receptor affinity and selectivity versus D2 and alpha1 receptors. Part 6. Perrone, R., Berardi, F., Colabufo, N.A., Leopoldo, M., Tortorella, V. Bioorg. Med. Chem. (2000) [Pubmed]
 
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