Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Antonio M. Fregnan"'
Autor:
Lhaís A. Caldas, Patricia D. Santos, Elaine R. Carbonero, Marisa Ionta, Marta Miyazawa, Ester S. Caixeta, Antonio M. Fregnan, Bianca Barros Nóbrega, Maria Carolina B. Di Medeiros, Nelson Menolli, Douglas M. M. Soares, Cassius V. Stevani, Patricia Sartorelli
Publikováno v:
Pharmaceuticals, Vol 15, Iss 10, p 1179 (2022)
Gymnopilus consists of a widely distributed genus of basidiomycetes, especially in tropical regions of the world, such as Japan, Australia, Paraguay, and Brazil. This genus biosynthesizes interesting bioactive compounds, such as sesquiterpenoids, oli
Externí odkaz:
https://doaj.org/article/cda1407a5f3b497ca9ee60698bf545d8
Autor:
Alexandre F. C. Galvão, Milena Botelho Pereira Soares, Luiz Felipe Leomil Coelho, Antonio M. Fregnan, Daniel P. Bezerra, Thiago Belarmino de Souza, Amanda Latercia Tranches Dias, Stella Maria de Souza Morais, Diogo Rodrigo de Magalhães Moreira, Danielle Ferreira Dias, Guilherme Andrade Brancaglion, Diogo Teixeira Carvalho, Josidel Conceição Oliver, Naiara Chaves Silva, Cinara Oliveira D’Sousa Costa
Publikováno v:
Medicinal Chemistry Research. 26:603-614
In this work it is described the synthesis, characterization and antimicrobial and toxicity evaluation of a series of analogs of piplartine, a piperamide found in Piper sp. The compounds structures were confirmed by infrared spectroscopy, 1H, 13C nuc
Autor:
Letícia de Almeida, Teodorico C. Ramalho, Juliana O. S. Giacoppo, Isael Aparecido Rosa, Antonio M. Fregnan, Diogo Teixeira Carvalho, Marcos José Marques, Marcelo Henrique dos Santos, Karina Ferreira Alves, Claudinei Alves da Silva da Silva
Publikováno v:
LOCUS Repositório Institucional da UFV
Universidade Federal de Viçosa (UFV)
instacron:UFV
Universidade Federal de Viçosa (UFV)
instacron:UFV
Eight coumarin derivatives (2–8) were synthesized from 7-hydroxy-4-phenylcoumarin 1 and were evaluated for their in vitro leishmanicidal activity against promastigote and amastigote forms of Leishmania amazonensis, as well their toxicity in murine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4400550c5c7de40cc0972138a1398f6
http://www.locus.ufv.br/handle/123456789/21872
http://www.locus.ufv.br/handle/123456789/21872
Autor:
Fernanda N. Silva, Antonio M. Fregnan, Pedro Henrique O. Abrão, Amanda Latercia Tranches Dias, Rafael Brianti Pizi, Diogo Teixeira Carvalho, Naiara Chaves Silva, Luiz Felipe Leomil Coelho, Thiago Belarmino de Souza, Marcia Paranho Veloso, Luiz Cosme Cotta Malaquias, Danielle Ferreira Dias
Publikováno v:
Chemical biologydrug design. 86(4)
New Mannich base-type eugenol derivatives were synthesized and evaluated for their anticandidal activity using a broth microdilution assay. Among the synthesized compounds, 4-allyl-2-methoxy-6-(morpholin-4-ylmethyl) phenyl benzoate (7) and 4-{5-allyl