G. Aguirre

发表

Platinum-based complexes of bioactive 3-(5-nitrofuryl)acroleine thiosemicarbazones showing anti-Trypanosoma cruzi activity.

M. Vieites, D. Gambino, H. Cerecetto, 2009, Journal of inorganic biochemistry.

Platinum(II) metal complexes as potential anti-Trypanosoma cruzi agents.

B. Garat, M. Vieites, D. Gambino, 2008, Journal of inorganic biochemistry.

In vitro activity and mechanism of action against the protozoan parasite Trypanosoma cruzi of 5-nitrofuryl containing thiosemicarbazones.

A. Denicola, Marcelo Fernández, D. Gambino, 2004, Bioorganic & medicinal chemistry.

Pyrimido[1,2-a]quinoxaline 6-oxide and phenazine 5,10-dioxide derivatives and related compounds as growth inhibitors of Trypanosoma cruzi.

H. Cerecetto, L. Boiani, Mercedes González, 2008, European journal of medicinal chemistry.

Synthesis, trypanocidal activity and docking studies of novel quinoxaline-N-acylhydrazones, designed as cruzain inhibitors candidates.

N. Romeiro, L. M. Lima, E. Barreiro, 2009, Bioorganic & medicinal chemistry.

Furoxan-, alkylnitrate-derivatives and related compounds as anti-trypanosomatid agents: mechanism of action studies.

M. Bertinaria, J. Cazzulo, H. Cerecetto, 2008, Bioorganic & medicinal chemistry.

Novel Antiprotozoal Products: Imidazole and Benzimidazole N‐Oxide Derivatives and Related Compounds

J. Nogal, J. Escario, A. Denicola, 2004, Archiv der Pharmazie.

New potent 5-substituted benzofuroxans as inhibitors of Trypanosoma cruzi growth: quantitative structure-activity relationship studies.

E. Barreiro, E. Castellano, A. Denicola, 2005, Bioorganic & medicinal chemistry.

Quinoxaline N,N'-dioxide derivatives and related compounds as growth inhibitors of Trypanosoma cruzi. Structure-activity relationships.

H. Cerecetto, I. Aldana, M. A. Ortega, 2004, Bioorganic & medicinal chemistry letters.

4-nitroacetophenone-derived thiosemicarbazones and their copper(II) complexes with significant in vitro anti-trypanosomal activity.

A. Mangrich, A. Batista, A. M. Ferreira, 2008, European journal of medicinal chemistry.

Potent in vitro anti-Trypanosoma cruzi activity of pyridine-2-thiol N-oxide metal complexes having an inhibitory effect on parasite-specific fumarate reductase

A. Gómez-Barrio, B. Garat, P. Smircich, 2008, JBIC Journal of Biological Inorganic Chemistry.

Improving anti-trypanosomal activity of 3-aminoquinoxaline-2-carbonitrile N1,N4-dioxide derivatives by complexation with vanadium.

M. H. Torre, G. Arrambide, A. Monge, 2006, Bioorganic & medicinal chemistry.

Indazole N-oxide derivatives as antiprotozoal agents: synthesis, biological evaluation and mechanism of action studies.

V. Arán, A. Monge, H. Cerecetto, 2006, Bioorganic & medicinal chemistry.

In vivo anti-Chagas vinylthio-, vinylsulfinyl-, and vinylsulfonylbenzofuroxan derivatives.

N. Campillo, R. Krauth-Siegel, J. Cazzulo, 2007, Journal of medicinal chemistry.

Nitrofurylsemicarbazone rhenium and ruthenium complexes as anti-trypanosomal agents.

A. Denicola, D. Gambino, H. Cerecetto, 2006, European journal of medicinal chemistry.

Second generation of 5-ethenylbenzofuroxan derivatives as inhibitors of Trypanosoma cruzi growth: synthesis, biological evaluation, and structure-activity relationships.

A. Merlino, H. Cerecetto, L. Boiani, 2007, Bioorganic & medicinal chemistry.

Furoxan derivatives as cytotoxic agents: preliminary in vivo antitumoral activity studies.

H. Cerecetto, J. P. Pacheco, G. Aguirre, 2006, Die Pharmazie.

Benzo[1,2-c]1,2,5-oxadiazole N-oxide derivatives as potential antitrypanosomal drugs. Part 3: Substituents-clustering methodology in the search for new active compounds.

A. Denicola, M. Möller, L. Thomson, 2005, Bioorganic & medicinal chemistry.

Design, synthesis and biological evaluation of new potent 5-nitrofuryl derivatives as anti-Trypanosoma cruzi agents. Studies of trypanothione binding site of trypanothione reductase as target for rational design.

V. Martínez-Merino, M. Gil, A. Denicola, 2004, European journal of medicinal chemistry.

Study of 5-nitroindazoles' anti-Trypanosoma cruzi mode of action: electrochemical behaviour and ESR spectroscopic studies.

V. Arán, H. Cerecetto, U. Kemmerling, 2009, European journal of medicinal chemistry.

Chromosome evolution in the annual killifish genus Cynolebias and mitochondrial phylogenetic analysis

A. Lalanne, G. García, G. Aguirre, 2004, Chromosome Research.

Ecotoxicological quality in sediments of Reloncaví and Corcovado gulfs, Chile

N. Silva, A. Rudolph, G. Aguirre, 2007 .

Culture-Dependent Bioprospecting of Bacterial Isolates From the Canadian High Arctic Displaying Antibacterial Activity

S. Gruenheid, L. Whyte, B. Boyle, 2019, Front. Microbiol..

Benzo[1, 2‐c]1, 2, 5‐oxadiazole N‐Oxide Derivatives as Potential Antitrypanosomal Drugs. Structure‐Activity Relationships. Part II

A. Denicola, G. Seoane, A. Monge, 2002, Archiv der Pharmazie.

New potent 5-nitrofuryl derivatives as inhibitors of Trypanosoma cruzi growth. 3D-QSAR (CoMFA) studies.

E. Barreiro, A. Denicola, H. Cerecetto, 2006, European journal of medicinal chemistry.

Benzo[1,2‐c]1,2,5‐oxadiazole N‐Oxide Derivatives as Potential Antitrypanosomal Drugs. Structure—Activity Relationships. Part 2.

A. Denicola, G. Seoane, A. Monge, 2002 .

5-Nitro-2-furyl derivative actives against Trypanosoma cruzi: preliminary in vivo studies.

Marcelo Fernández, H. Cerecetto, Mercedes González, 2009, European journal of medicinal chemistry.

ESR AND SPIN TRAPPING STUDIES OF TWO NEW POTENTIAL NTITRYPANOSOMAL DRUGS

H. Cerecetto, J. Maya, Mercedes González, 2003 .

Effects of cyclohexane, an industrial solvent, on the yeast Saccharomyces cerevisiae and on isolated yeast mitochondria

P. Rangel, S. Uribe, G. Aguirre, 1990, Applied and environmental microbiology.