Lista de obras - Bruno J. Neves - Dominio Público Uruguay

Analogues of Marine Guanidine Alkaloids Are in Vitro Effective against Trypanosoma cruzi and Selectively Eliminate Leishmania (L.) infantum Intracellular Amastigotes

artículo científico publicado en 2016

Antitrypanosomal activity and evaluation of the mechanism of action of dehydrodieugenol isolated from Nectandra leucantha (Lauraceae) and its methylated derivative against Trypanosoma cruzi.

artículo científico publicado en 2016

Artificial intelligence systems for the design of magic shotgun drugs

artículo científico publicado en 2023

Artificial intelligence-guided Approach for Efficient Virtual Screening of Hits Against <i>Schistosoma Mansoni</i>

artículo científico publicado en 2023

Blocking the L-type Ca2+ channel (Cav 1.2) is the key mechanism for the vascular relaxing effect of Pterodon spp. and its isolated diterpene methyl-6α-acetoxy-7β-hydroxyvouacapan-17β-oate

artículo científico publicado en 2015

Chalcone Derivatives: Promising Starting Points for Drug Design.

artículo científico publicado en 2017

Chalcones as a basis for computer-aided drug design: innovative approaches to tackle malaria

scientific article published on 26 September 2019

Computer-aided discovery of two novel chalcone-like compounds active and selective against Leishmania infantum

artículo científico publicado en 2017

Deep Learning-driven research for drug discovery: Tackling Malaria

scientific article published on 18 February 2020

Discovery of New Anti-Schistosomal Hits by Integration of QSAR-Based Virtual Screening and High Content Screening

artículo científico publicado en 2016

Discovery of New Zika Protease and Polymerase Inhibitors through the Open Science Collaboration Project OpenZika

artículo científico publicado en 2022

Discovery of new potential hits of Plasmodium falciparum enoyl-ACP reductase through ligand- and structure-based drug design approaches

artículo científico publicado en 2013

Déjà vu: Stimulating open drug discovery for SARS-CoV-2

scientific article published on 19 April 2020

Illustrating and homology modeling the proteins of the Zika virus

artículo científico publicado en 2016

In silico repositioning-chemogenomics strategy identifies new drugs with potential activity against multiple life stages of Schistosoma mansoni

artículo científico publicado en 2015

In vitro, in silico and in vivo analysis of novel aromatic amidines against Trypanosoma cruzi

artículo científico publicado en 2017

Modern approaches to accelerate discovery of new antischistosomal drugs.

artículo científico publicado en 2016

Natural Compounds as Non-Nucleoside Inhibitors of Zika Virus Polymerase through Integration of In Silico and In Vitro Approaches

scientific article published in 2022

Natural products as leads in schistosome drug discovery.

artículo científico publicado en 2015

Neolignans from leaves of Nectandra leucantha (Lauraceae) display in vitro antitrypanosomal activity via plasma membrane and mitochondrial damages.

artículo científico publicado en 2017

QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni

scientific article published on 02 June 2016

QSAR-driven design, synthesis and discovery of potent chalcone derivatives with antitubercular activity

artículo científico publicado en 2017

Repositioning of new potential schistosomicidal drugs using chemogenomic strategy

artículo científico publicado en 2014

Structural and chemical basis for enhanced affinity to a series of mycobacterial thymidine monophosphate kinase inhibitors: fragment-based QSAR and QM/MM docking studies

artículo científico publicado en 2012

The antidepressant drug paroxetine as a new lead candidate in schistosome drug discovery

article published in 2016

Unveiling the Antiviral Capabilities of Targeting Human Dihydroorotate Dehydrogenase against SARS-CoV-2

artículo científico publicado en 2024

Lista de obras de Bruno J. Neves

Analogues of Marine Guanidine Alkaloids Are in Vitro Effective against Trypanosoma cruzi and Selectively Eliminate Leishmania (L.) infantum Intracellular Amastigotes

Antitrypanosomal activity and evaluation of the mechanism of action of dehydrodieugenol isolated from Nectandra leucantha (Lauraceae) and its methylated derivative against Trypanosoma cruzi.

Artificial intelligence systems for the design of magic shotgun drugs

Artificial intelligence-guided Approach for Efficient Virtual Screening of Hits Against <i>Schistosoma Mansoni</i>

Blocking the L-type Ca2+ channel (Cav 1.2) is the key mechanism for the vascular relaxing effect of Pterodon spp. and its isolated diterpene methyl-6α-acetoxy-7β-hydroxyvouacapan-17β-oate

Chalcone Derivatives: Promising Starting Points for Drug Design.

Chalcones as a basis for computer-aided drug design: innovative approaches to tackle malaria

Computer-aided discovery of two novel chalcone-like compounds active and selective against Leishmania infantum

Deep Learning-driven research for drug discovery: Tackling Malaria

Discovery of New Anti-Schistosomal Hits by Integration of QSAR-Based Virtual Screening and High Content Screening

Discovery of New Zika Protease and Polymerase Inhibitors through the Open Science Collaboration Project OpenZika

Discovery of new potential hits of Plasmodium falciparum enoyl-ACP reductase through ligand- and structure-based drug design approaches

Déjà vu: Stimulating open drug discovery for SARS-CoV-2

Illustrating and homology modeling the proteins of the Zika virus

In silico repositioning-chemogenomics strategy identifies new drugs with potential activity against multiple life stages of Schistosoma mansoni

In vitro, in silico and in vivo analysis of novel aromatic amidines against Trypanosoma cruzi

Modern approaches to accelerate discovery of new antischistosomal drugs.

Natural Compounds as Non-Nucleoside Inhibitors of Zika Virus Polymerase through Integration of In Silico and In Vitro Approaches

Natural products as leads in schistosome drug discovery.

Neolignans from leaves of Nectandra leucantha (Lauraceae) display in vitro antitrypanosomal activity via plasma membrane and mitochondrial damages.

QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni

QSAR-driven design, synthesis and discovery of potent chalcone derivatives with antitubercular activity

Repositioning of new potential schistosomicidal drugs using chemogenomic strategy

Structural and chemical basis for enhanced affinity to a series of mycobacterial thymidine monophosphate kinase inhibitors: fragment-based QSAR and QM/MM docking studies

The antidepressant drug paroxetine as a new lead candidate in schistosome drug discovery

Unveiling the Antiviral Capabilities of Targeting Human Dihydroorotate Dehydrogenase against SARS-CoV-2