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1
Receptor-dependent LQTA-QSAR applied to a set of phenothiazine derivatives as inhibitors of T. cruzi trypanothione reductase
Receptor-dependent LQTA-QSAR applied to a set of phenothiazine derivatives as inhibitors of T. cruzi trypanothione reductase
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Receptor-dependent LQTA-QSAR applied to a set of phenothiazine derivatives as inhibitors of T. cruzi trypanothione reductase

Euzébio Guimarães Barbosa Kerly Fernanda Mesquita Pasqualoto; Elizabeth Igne Ferreira; Márcia Miguel Castro Ferreira; Science and Pharmaceutical Technology Meeting of the Faculty of the Pharmaceutical Sciences of the University of São Paulo (14. 2009 São Paulo); São Paulo Pharmacy and Biochemistry Universitary Meeting (44. 2009 São Paulo); Annual Research Symposium on Pharmaceutical Sciences (44. 2009 São Paulo)

Brazilian Journal of Pharmaceutical Sciences São Paulo v. 45, suppl. 1, p. 43, res. FCF082, 2009

São Paulo 2009

Item não circula. Consulte sua biblioteca.(Acessar)

2
5-Nitro-2-furfuriliden derivates as potent antileishmanial agents in vitro evaluation and structure-activity relationship analyses
5-Nitro-2-furfuriliden derivates as potent antileishmanial agents in vitro evaluation and structure-activity relationship analyses
Material Type:
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5-Nitro-2-furfuriliden derivates as potent antileishmanial agents in vitro evaluation and structure-activity relationship analyses

Carolina Arruda Braz Bianca Zingales; Euzébio Guimarães Barbosa; José Angelo Lauletta Lindoso; Leoberto Costa Tavares; Congress of the Brazilian Association of Pharmaceutical Sciences/ABCF (4. 2018 São Paulo)

Brazilian Journal of Pharmaceutical Sciences São Paulo v. 54, suppl. 2, p. res. , 2018

São Paulo 2018

Acesso online

3
Design of arylsulfonylhydrazones as potential FabH inhibitors synthesis, antimicrobial evaluation and molecular docking
Design of arylsulfonylhydrazones as potential FabH inhibitors synthesis, antimicrobial evaluation and molecular docking
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Artigo 		Adicionar ao Meu Espaço

Design of arylsulfonylhydrazones as potential FabH inhibitors synthesis, antimicrobial evaluation and molecular docking

Thais Batista Fernandes Natanael Dante Segretti; Felipe Rebello Lourenço; Thalita Marcílio Cândido; André Rolim Baby; Euzébio Guimarães Barbosa; Roberto Parise Filho

Medicinal Chemistry Sharjay v. 17, p. 474-484, 2021

Sharjay 2021

Item não circula. Consulte sua biblioteca.(Acessar)

4
Synthesis, molecular modeling, and evaluation of novel sulfonylhydrazones as acetylcholinesterase inhibitors for Alzheimer's disease
Synthesis, molecular modeling, and evaluation of novel sulfonylhydrazones as acetylcholinesterase inhibitors for Alzheimer's disease
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Artigo 		Adicionar ao Meu Espaço

Synthesis, molecular modeling, and evaluation of novel sulfonylhydrazones as acetylcholinesterase inhibitors for Alzheimer's disease

Thais Batista Fernandes Micael Rodrigues Cunha; Renata P Sakata; Thalita Marcílio Cândido; André Rolim Baby; Mauricio Temotheo Tavares; Euzébio Guimarães Barbosa; Wanda P Almeida; Roberto Parise Filho

Archiv der Pharmazie Chemistry in Life Science Weinheim v. 350, n. 11, p. 1-16 art.e1700163, 2017

Weinheim 2017

Item não circula. Consulte sua biblioteca.(Acessar)

5
Theoretical investigations of the disassembly behavior of targeted dendrimer potentially antichagasic
Theoretical investigations of the disassembly behavior of targeted dendrimer potentially antichagasic
Material Type:
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Theoretical investigations of the disassembly behavior of targeted dendrimer potentially antichagasic

Jeanine Giarolla Vanessa Almeida Otelo; Edjan Carlos Dantas da Silva; Elizabeth Igne Ferreira; Euzébio Guimarães Barbosa; World Chemistry Congress (46. 2017 São Paulo); Reunião Anual da Sociedade Brasileira de Química (SBQ) (40. 2017 São Paulo); IUPAC General Assembly (49. 2017 São Paulo)

Proceedings Durham : International Union of Pure and Applied Chemistry (IUPAC), 2017

Durham International Union of Pure and Applied Chemistry IUPAC 2017

Item não circula. Consulte sua biblioteca.(Acessar)

6
Exploratory data analysis of a 5-nitro furfuriliden library with action against Leishmania infantum promastigotes
Exploratory data analysis of a 5-nitro furfuriliden library with action against Leishmania infantum promastigotes
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Exploratory data analysis of a 5-nitro furfuriliden library with action against Leishmania infantum promastigotes

Carolina Arruda Braz Euzébio Guimarães Barbosa; José Angelo Lauletta Lindoso; Leoberto Costa Tavares; Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo (23. 2018 São Paulo); Annual Research Symposium on Pharmaceutical Sciences (10. 2018 São Paulo)

Brazilian Journal of Pharmaceutical Sciences São Paulo v. 54, suppl. 1, p. 34 res. FCF063, 2018

São Paulo 2018

Item não circula. Consulte sua biblioteca.(Acessar)

7
Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells design, synthesis and molecular modeling
Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells design, synthesis and molecular modeling
Material Type:
Artigo 		Adicionar ao Meu Espaço

Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells design, synthesis and molecular modeling

Gustavo José Vasco Pereira Maurício Temotheo Tavares; Ricardo Alexandre de Azevedo; Barbara Behr Martins; Micael Rodrigues Cunha; Rajesh Bhardwaj; Yara Cury; Vanessa Olzon Zambelli; Euzébio Guimarães Barbosa; Matthias A Hediger; Roberto Parise Filho

Bioorganic and Medicinal Chemistry Oxford v. 27, n. 13, p. 2893-2904, 2019

Oxford 2019

Item não circula. Consulte sua biblioteca.(Acessar)

8
Synthesis, molecular modeling and evaluation of novel sulfonylhydrazones as acethylcholinesterase inhibitors for alzheimer’s disease tratment
Synthesis, molecular modeling and evaluation of novel sulfonylhydrazones as acethylcholinesterase inhibitors for alzheimer’s disease tratment
Material Type:
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Synthesis, molecular modeling and evaluation of novel sulfonylhydrazones as acethylcholinesterase inhibitors for alzheimer’s disease tratment

Thais Batista Fernandes Micael Rodrigues Cunha; Renata P Sakata; Thalita Marcílio Cândido; André Rolim Baby; Euzébio Guimarães Barbosa; Wanda P Almeida; Roberto Parise Filho; Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo (22. 2017 São Paulo); Annual Research Symposium on Pharmaceutical Sciences (9. 2017 São Paulo)

Brazilian Journal of Pharmaceutical Sciences São Paulo v. 53, suppl. 1, p. 54 res. FCF103, 2017

São Paulo 2017

Item não circula. Consulte sua biblioteca.(Acessar)

9
Scaffold repositioning of spiro-acridine derivatives as fungi chitinase inhibitor by target fishing and in vitro studies
Scaffold repositioning of spiro-acridine derivatives as fungi chitinase inhibitor by target fishing and in vitro studies
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Scaffold repositioning of spiro-acridine derivatives as fungi chitinase inhibitor by target fishing and in vitro studies

de Oliveira Viana, Jéssika ; Silva E Souza, Eden ; Sbaraini, Nicolau ; Vainstein, Marilene Henning ; Gomes, Joilly Nilce Santana ; de Moura, Ricardo Olímpio ; Barbosa, Euzébio Guimarães

Scientific reports, 2023-05, Vol.13 (1), p.7320-7320, Article 7320 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Spiro‐Acridine Compound as a Pteridine Reductase 1 Inhibitor: in silico Target Fishing and in vitro Studies
Spiro‐Acridine Compound as a Pteridine Reductase 1 Inhibitor: in silico Target Fishing and in vitro Studies
Material Type:
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Spiro‐Acridine Compound as a Pteridine Reductase 1 Inhibitor: in silico Target Fishing and in vitro Studies

Oliveira Viana, Jéssika ; Sena Mendes, Marina ; Santos Castilho, Marcelo ; Olímpio de Moura, Ricardo ; Guimarães Barbosa, Euzébio

ChemMedChem, 2024-06, Vol.19 (11), p.e202300545-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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Deste Autor:

  1. Barbosa, E
  2. Parise Filho, R
  3. Baby, A
  4. Fernandes, T
  5. Cândido, T

Neste Assunto:

  1. Science & Technology
  2. Life Sciences & Biomedicine
  3. Physical Sciences
  4. Pharmacology & Pharmacy
  5. Chemistry

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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