V
Vanessa de Andrade Royo
Researcher at Unimontes
Publications - 59
Citations - 557
Vanessa de Andrade Royo is an academic researcher from Unimontes. The author has contributed to research in topics: Population & Genetic structure. The author has an hindex of 11, co-authored 51 publications receiving 479 citations. Previous affiliations of Vanessa de Andrade Royo include University of São Paulo.
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Journal ArticleDOI
In vivo analgesic and anti-inflammatory activities of ursolic acid and oleanoic acid from Miconia albicans (Melastomataceae).
M. A. L. Vasconcelos,Vanessa de Andrade Royo,Daniele da Silva Ferreira,Antônio Eduardo Miller Crotti,Márcio Luis Andrade e Silva,José Carlos Tavares Carvalho,Jairo Kenupp Bastos,Wilson Roberto Cunha +7 more
TL;DR: It is suggested that other compounds, rather than UA and OA, should be responsible for the evaluated activities in the crude extract of Miconia albicans aerial parts, since the crude Extract samples displayed good activities.
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Trypanocidal activity of (-)-cubebin derivatives against free amastigote forms of Trypanosoma cruzi.
Vanessa A. Souza,Rosangela da Silva,Ana C. Pereira,Vanessa de Andrade Royo,Juliana Saraiva,Marisa Montanheiro,Gustavo Henrique Bianco de Souza,Ademar A. da Silva Filho,Marcella D. Grando,Paulo Marcos Donate,Jairo Kenupp Bastos,Sérgio de Albuquerque,Márcio Luis Andrade e Silva +12 more
TL;DR: Five (-)-cubebin derivative compounds, (-)-O-acetyl cubebin (3), (-)-N,N-dimethylaminoethyl-cub Pastebin (5), (--hinokinin (6) and (-)-6,6'-dinitrohinokin in (7), previously synthesised by the research group, were evaluated on in vitro assay against free amastigote forms of Trypanosoma cruzi.
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Evaluation of piper cubeba extract, (-)-cubebin and its semi-synthetic derivatives against oral pathogens.
Márcio Luis Andrade e Silva,H. S. Coímbra,A. C. Pereira,V. A. Almeida,Thais C. Lima,Eveline S. Costa,A. H. C. Vinhólis,Vanessa de Andrade Royo,R. Silva,Ademar A. da Silva Filho,Wilson Roberto Cunha,Niege Araçari Jacometti Cardoso Furtado,Carlos Henrique Gomes Martins,Tereza Cristina Melo de Brito Carvalho,Jairo Kenupp Bastos +14 more
TL;DR: The semi‐synthetic derivative of (‐)‐6,6′‐dinitrohinokinin was the most active compound against all the evaluated microorganisms and it may be suggested that the presence of the carbonyl group at C‐9 plus the introduction of polar groups in the aromatic rings improve the antimicrobial activity of dibenzylbutyrolactone compounds.
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Hinokinin causes antigenotoxicity but not genotoxicity in peripheral blood of Wistar rats.
Jamile Ferraris Medola,Vívian Pedigone Cintra,Érika Patrı´cia Pesqueira e Silva,Vanessa de Andrade Royo,Rosângela Silva,Juliana Saraiva,Sérgio de Albuquerque,Jairo Kenupp Bastos,Márcio Luis Andrade e Silva,Denise Crispim Tavares +9 more
TL;DR: The present study shows that (-)-hinokinin not only has no genotoxic effect, but is also effective in reducing the chromosome damage induced by the chemotherapeutic agent doxorubicin (DXR).
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In vivo analgesic activity, toxicity and phytochemical screening of the hydroalcoholic extract from the leaves of Psidium cattleianum Sabine
Felipe Queiroz Alvarenga,Bárbara Caroline Ferreira Mota,Marcel Nani Leite,Jaciara M.S. Fonseca,Dario Alves de Oliveira,Vanessa de Andrade Royo,Márcio Luis Andrade e Silva,Viviane Rodrigues Esperandim,Alexandre Luiz Souto Borges,Rosangela da Silva de Laurentiz +9 more
TL;DR: The results of the experimental studies proved the analgesic activity of ELPCS and supported the traditional use of this plant.