Luiz C. S. Pinheiro

发表

Plasmodium falciparum dihydroorotate dehydrogenase: a drug target against malaria.

M. Nonato, N. Boechat, F. A. Calil, 2018, Future medicinal chemistry.

Conformation differences in N-[2-(1-arenesulfonyl-1H-pyrazol-3-yl)-6-methyl-phenyl]-arenesulfonamides, (arene = benzene and 4-toluene)

J. C. Borges, J. Wardell, S. Wardell, 2014 .

Current Antimalarial Therapies and Advances in the Development of Semi-Synthetic Artemisinin Derivatives.

N. Boechat, Luiz C. S. Pinheiro, Lívia M. Feitosa, 2018, Anais da Academia Brasileira de Ciencias.

Design, synthesis, and antiviral activity of new 1H-1,2,3-triazole nucleoside ribavirin analogs

O. Santos-Filho, V. Ferreira, C. Sacramento, 2013, Medicinal Chemistry Research.

Synthesis and anti-HSV-1 evaluation of new 3H-benzo[b]pyrazolo[3,4-h]-1,6-naphthyridines and 3H-pyrido[2,3-b]pyrazolo[3,4-h]-1,6-naphthyridines

J. C. Borges, M. S. Dos Santos, Alice M. R. Bernardino, 2012, Organic and medicinal chemistry letters.

Synthesis and in vitro evaluation of new benzenesulfonamides as antileishmanial agents

H. Castro, J. C. Borges, L. Leon, 2014 .

An Efficient Synthesis of New 5‐(1‐Aryl‐1H‐pyrazole‐4‐yl)‐1H‐tetrazoles from 1‐Aryl‐1H‐pyrazole‐4‐carbonitriles via [3 + 2] Cycloaddition Reaction

L. Leon, A. Bernardino, M. Canto-Cavalheiro, 2012 .

Crystal structures of two anhydrous and one hydrated 7-(arylamino)-5-methyl-2-(trifluoromethyl)-[1,2,4]-triazolo-[1,5-a]pyrimidine derivatives

Â. Pinto, J. Wardell, S. Wardell, 2014 .

Synthetic compounds with sulfonamide moiety against Leishmaniasis: an overview

N. Boechat, Maria de Lourdes G. Ferreira, Luiz C. S. Pinheiro, 2019, Medicinal Chemistry Research.

New Trifluoromethyl Triazolopyrimidines as Anti-Plasmodiumfalciparum Agents

Â. Pinto, O. Santos-Filho, A. Krettli, 2012, Molecules.

Design and Synthesis of New N-(5-Trifluoromethyl)-1H-1,2,4-triazol-3-yl Benzenesulfonamides as Possible Antimalarial Prototypes

O. Santos-Filho, N. Boechat, Luiz C. S. Pinheiro, 2011, Molecules.

New pyrazolopyrimidine derivatives as Leishmania amazonensis arginase inhibitors.

N. Boechat, E. R. da Silva, M. N. Soeiro, 2019, Bioorganic & medicinal chemistry.

Design, synthesis and anti-P. falciparum activity of pyrazolopyridine-sulfonamide derivatives.

A. Bernardino, N. Boechat, L. Carvalho, 2016, Bioorganic & medicinal chemistry.

New Compounds Hybrids 1H‐1,2,3‐Triazole‐Quinoline Against Plasmodium falciparum

A. Krettli, N. Boechat, Luiz C. S. Pinheiro, 2014, Chemical biology & drug design.

Synthesis, Crystal Structures, and in Silico Toxicity Prediction of Thienopyridine Phosphoramidates

J. Resende, G. Guedes, Luiz C. S. Pinheiro, 2013 .

Design, synthesis, and antiviral activity of new 1H-1,2,3-triazole nucleoside ribavirin analogs

O. Santos-Filho, V. Ferreira, C. Sacramento, 2014, Medicinal Chemistry Research.

Novel Selective Inhibitor of Leishmania (Leishmania) amazonensis Arginase

N. Boechat, M. Bastos, Carolina C. P. Costa, 2015, Chemical biology & drug design.

Antimalarial and anti-inflammatory activities of new chloroquine and primaquine hybrids: Targeting the blockade of malaria parasite transmission.

L. N. Seito, A. Krettli, N. Boechat, 2020, Bioorganic & medicinal chemistry.

Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors.

M. G. Albuquerque, M. Nonato, Rafael V. C. Guido, 2020, European journal of medicinal chemistry.

SYNTHESIS AND ANTIVIRAL ACTIVITY OF NEW 4- (PHENYLAMINO)THIENO[2,3-b]PYRIDINE DERIVATIVES

V. Ferreira, A. Bernardino, Luiz C. S. Pinheiro, 2004 .

New simplex Type 1 lytic infection pyridine system derivative as a novel goal against Herpes

Cláudio Cirne-Santos, Caroline Barros, I. Paixão, 2017 .

N-(4-Chlorophenyl)-5-(4,5-dihydro-1H-imidazol-2-yl)thieno[2,3-b]pyridin-4-amine

E. Tiekink, J. Wardell, S. Wardell, 2012, Acta crystallographica. Section E, Structure reports online.

New pentasubstituted pyrrole hybrid atorvastatin-quinoline derivatives with antiplasmodial activity.

C. Kaiser, A. Krettli, N. Boechat, 2016, Bioorganic & medicinal chemistry letters.

Anti-Plasmodium falciparum activity of quinoline-sulfonamide hybrids.

A. Krettli, N. B. Souza, N. Boechat, 2015, Bioorganic & medicinal chemistry.

Synthesis, Biological Evaluation, and Molecular Modeling Studies of New Thiadiazole Derivatives as Potent P2X7 Receptor Inhibitors

H. Castro, C. R. Rodrigues, R. Faria, 2019, Front. Chem..

Synthesis of benzoylthiourea derivatives and analysis of their antibacterial performance against planktonic Staphylococcus aureus and its biofilms

N. Boechat, D. Sachs, F. Aguiar-Alves, 2020, Letters in applied microbiology.

Synthesis and anti-Plasmodium falciparum evaluation of novel pyrazolopyrimidine derivatives

N. Boechat, L. Carvalho, Luiz C. S. Pinheiro, 2018, Medicinal Chemistry Research.

Current Antimalarial Therapies and Advances in the Development of Semi-Synthetic Artemisinin Derivatives.

N. Boechat, Luiz C. S. Pinheiro, Lívia M. Feitosa, 2018, Anais da Academia Brasileira de Ciencias.

Crystal structures of two anhydrous and one hydrated 7-(arylamino)-5-methyl-2-(trifluoromethyl)-[1,2,4]-triazolo-[1,5-a]pyrimidine derivatives

J. Wardell, S. Wardell, N. Boechat, 2014 .

New pentasubstituted pyrrole hybrid atorvastatin-quinoline derivatives with antiplasmodial activity.

C. Kaiser, A. Krettli, N. Boechat, 2016, Bioorganic & medicinal chemistry letters.