F. C. Santos

发表

1,2:5,6-Di-O-isopropylidene-3-C-methyl-α-d-allofuranose

V. Ferreira, L. Forezi, M. de Souza, 2013, Acta crystallographica. Section E, Structure reports online.

Design, synthesis, and biological evaluation of new 3-hydroxy-2-oxo-3-trifluoromethylindole as potential HIV-1 reverse transcriptase inhibitors

N. Romeiro, I. Frugulhetti, T. Souza, 2007, Medicinal Chemistry Research.

Docking of anti-HIV-1 oxoquinoline-acylhydrazone derivatives as potential HSV-1 DNA polymerase inhibitors

M. G. Albuquerque, Cláudio Cirne-Santos, I. Paixão, 2014 .

Synthesis, biological, and theoretical evaluations of new 1,2,3-triazoles against the hemolytic profile of the Lachesis muta snake venom.

H. Castro, C. R. Rodrigues, A. Fuly, 2009, Bioorganic & medicinal chemistry.

Synthesis, antiviral activity and molecular modeling of oxoquinoline derivatives.

H. Castro, C. R. Rodrigues, Cláudio Cirne-Santos, 2009, Bioorganic & medicinal chemistry.

Synthesis of porphyrin–quinolone conjugates

M. Neves, A. Tomé, J. Cavaleiro, 2008 .

Conformational analysis of a quinolonic ribonucleoside with anti-HSV-1 activity

M. G. Albuquerque, V. Ferreira, A. Cunha, 2011 .

Molecular design, synthesis and biological evaluation of 1,4-dihydro-4-oxoquinoline ribonucleosides as TcGAPDH inhibitors with trypanocidal activity.

V. Ferreira, A. Leitão, J. S. da Silva, 2013, Bioorganic & medicinal chemistry letters.

Synthesis and Anti-HSV-1 Activity of 1,4-dihydro-4-oxoquinoline Ribonucleosides

G. Romeiro, V. Ferreira, A. Cunha, 2007 .

Synthesis and characterization of new porphyrin/4-quinolone conjugates

A. Gomes, M. Neves, A. Tomé, 2011 .

Oxoquinoline Derivatives: Identification and Structure–Activity Relationship (SAR) Analysis of New Anti-HSV-1 Agents

H. Castro, C. R. Rodrigues, V. Ferreira, 2011, Current Microbiology.