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European Journal of Medicinal Chemistry
|
December 4, 2017
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases
Laura De Luca, Francesca Mancuso, Stefania Ferro, et al.
Chemmedchem
|
September 4, 2008
Computational studies to discover a new NR2B/NMDA receptor antagonist and evaluation of pharmacological profile
Rosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Journal of Medicinal Chemistry
|
March 27, 2012
Synthesis, structure-activity relationship studies, and X-ray crystallographic analysis of arylsulfonamides as potent carbonic anhydrase inhibitors
Rosaria Gitto, Francesca M Damiano, Pavel Mader, et al.
European Journal of Medicinal Chemistry
|
August 16, 2015
Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms
Maria Rosa Buemi, Laura De Luca, Stefania Ferro, et al.
European Journal of Medicinal Chemistry
|
April 8, 2014
Diketoacid chelating ligands as dual inhibitors of HIV-1 integration process
Dominga Rogolino, Mauro Carcelli, Carlotta Compari, et al.
European Journal of Medicinal Chemistry
|
November 5, 2016
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors
Stefania Ferro, Laura De Luca, Maria Paola Germanò, et al.
Chemmedchem
|
February 27, 2016
In Vivo Evaluation of Selective Carbonic Anhydrase Inhibitors as Potential Anticonvulsant Agents
Elvira Bruno, Maria R Buemi, Laura De Luca, et al.
Journal of Medicinal Chemistry
|
December 14, 2004
Synthesis and antibacterial activity of new poly-S-lysine-porphyrin conjugates
João P C Tomé, Maria G P M S Neves, Augusto C Tomé, et al.
Bioorganic & Medicinal Chemistry
|
January 14, 2014
Synthesis, modelling and biological characterization of 3-substituted-1H-indoles as ligands of GluN2B-containing N-methyl-d-aspartate receptors
Rosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Bioorganic & Medicinal Chemistry
|
July 1, 2008
Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors
Anna-Maria Monforte, Angela Rao, Patrizia Logoteta, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 73) with videos related to
Sort By:
Page
of 8
European Journal of Medicinal Chemistry
|
December 4, 2017
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases
Laura De Luca, Francesca Mancuso, Stefania Ferro, et al.
Chemmedchem
|
September 4, 2008
Computational studies to discover a new NR2B/NMDA receptor antagonist and evaluation of pharmacological profile
Rosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Journal of Medicinal Chemistry
|
March 27, 2012
Synthesis, structure-activity relationship studies, and X-ray crystallographic analysis of arylsulfonamides as potent carbonic anhydrase inhibitors
Rosaria Gitto, Francesca M Damiano, Pavel Mader, et al.
European Journal of Medicinal Chemistry
|
August 16, 2015
Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms
Maria Rosa Buemi, Laura De Luca, Stefania Ferro, et al.
European Journal of Medicinal Chemistry
|
April 8, 2014
Diketoacid chelating ligands as dual inhibitors of HIV-1 integration process
Dominga Rogolino, Mauro Carcelli, Carlotta Compari, et al.
European Journal of Medicinal Chemistry
|
November 5, 2016
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors
Stefania Ferro, Laura De Luca, Maria Paola Germanò, et al.
Chemmedchem
|
February 27, 2016
In Vivo Evaluation of Selective Carbonic Anhydrase Inhibitors as Potential Anticonvulsant Agents
Elvira Bruno, Maria R Buemi, Laura De Luca, et al.
Journal of Medicinal Chemistry
|
December 14, 2004
Synthesis and antibacterial activity of new poly-S-lysine-porphyrin conjugates
João P C Tomé, Maria G P M S Neves, Augusto C Tomé, et al.
Bioorganic & Medicinal Chemistry
|
January 14, 2014
Synthesis, modelling and biological characterization of 3-substituted-1H-indoles as ligands of GluN2B-containing N-methyl-d-aspartate receptors
Rosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Bioorganic & Medicinal Chemistry
|
July 1, 2008
Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors
Anna-Maria Monforte, Angela Rao, Patrizia Logoteta, et al.
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of 8