Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Mariana F. C. Cardoso"'
Autor:
Mário M. Q. Simões, Daniel T. G. Gonzaga, Mariana F. C. Cardoso, Luana da S. M. Forezi, Ana T. P. C. Gomes, Fernando de C. da Silva, Vítor F. Ferreira, Maria G. P. M. S. Neves, José A. S. Cavaleiro
Publikováno v:
Molecules, Vol 23, Iss 4, p 792 (2018)
Carbene transfer reactions are very important transformations in organic synthesis, allowing the generation of structurally challenging products by catalysed cyclopropanation, cyclopropenation, carbene C-H, N-H, O-H, S-H, and Si-H insertion, and olef
Externí odkaz:
https://doaj.org/article/b23789625ead447f91625da6b6f471e4
Autor:
Helena Silva, Natália Costa, Susana Nunes, Ângela Cunha, Carla Patinha, Mariana F. C. Cardoso
Publikováno v:
Annals of Applied Biology. 180:99-108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a0a217d9ad502f0b3df999f18fde28b
https://doi.org/10.1111/aab.12714
https://doi.org/10.1111/aab.12714
Autor:
Acácio S. de Souza, Vitor F. Ferreira, Mariana F. C. Cardoso, Ana Maria Caetano Faria, Robson Xavier Faria, Murilo Lamim Bello, Raíssa Maria Dos Santos Galvão, Luana da S. M. Forezi, Fernando Dias da Silva
Publikováno v:
Journal of the Brazilian Chemical Society.
Furanaphthoquinones are well known in medicinal chemistry for exhibiting relevant structural heterogeneity and bioactivities. In this work, it was synthesized a series of furanaphthoquinones through a tandem reaction between lawsone (8) and cyclic ke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d387ac236d63d03614ffe9b34f4fff68
https://doi.org/10.21577/0103-5053.20210142
https://doi.org/10.21577/0103-5053.20210142
Autor:
Vitor F. Ferreira, Fernando de C. da Silva, Rafael Ferreira Dantas, Mario Roberto Senger, Mariana F. C. Cardoso, Maria Cecília B. V. de Souza, Floriano P. Silva
Publikováno v:
Medicinal Chemistry Research. 28:1579-1588
In many cancer cells, glycoproteins show abnormal glycosylation patterns which have been associated with tumor initiation, progression, and metastasis. Thus, the glycosidases involved in glycoprotein maturation represent good targets for the developm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::143d41fc7da3d2a7c5d314fbdfe9bd0d
https://doi.org/10.1007/s00044-019-02396-4
https://doi.org/10.1007/s00044-019-02396-4
Autor:
Mariana F. C. Cardoso, Emerson Silva Lima, Daniel P. Bezerra, Caio César dos Santos Ferreira, Rosane Borges Dias, Clarissa Araújo Gurgel Rocha, Ludmila de Faro Valverde, Caroline Brandi Schlaepfer Sales, Fernando de C. da Silva, Milena Botelho Pereira Soares, Patrícia Danielle Oliveira de Almeida, Larissa Froede Brito, Gleyce dos Santos Barbosa Jobim, Vitor F. Ferreira, Lucas Rocha Bernardes, Marne Carvalho de Vasconcellos, Lirlândia P. Sousa
Publikováno v:
Chemico-biological interactions. 343
Quinones are plant-derived secondary metabolites that present diverse pharmacological properties, including antibacterial, antifungal, antiviral, anti-inflammatory, antipyretic and anticancer activities. In the present study, we evaluated the cytotox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f496aff1ff8c88bb946c4942151a8c0a
https://pubmed.ncbi.nlm.nih.gov/33939975
https://pubmed.ncbi.nlm.nih.gov/33939975
Autor:
Vitor F. Ferreira, Daniel T. G. Gonzaga, Fernando de C. da Silva, Mariana F. C. Cardoso, Luana da S. M. Forezi
Publikováno v:
Current Topics in Medicinal Chemistry. 18:1428-1453
Heterocyclic rings having nitrogen atoms are the molecular fragments most used in drug design by using the tools of medicinal chemistry. The 1,2,4-triazole rings are part of an extensive family of drugs that are in use in the pharmaceutical market. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93c340482255f5a79a0e628f7560e88
https://doi.org/10.2174/1568026618666180821143902
https://doi.org/10.2174/1568026618666180821143902
Autor:
Ana T. P. C. Gomes, Vitor F. Ferreira, Mário M.Q. Simões, Mariana F. C. Cardoso, José A. S. Cavaleiro, Daniel T. G. Gonzaga, Luana da S. M. Forezi, Maria G. P. M. S. Neves, Fernando de C. da Silva
Publikováno v:
Synthesis. 50:2678-2692
Carbenes and NHCs play an important role in porphyrin chemistry and several synthetically useful transformations leading to the preparation of new porphyrin derivatives have been developed. This short review presents an overview covering the literatu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcc70a3cec5513d61dc0ae2bbffe948a
https://doi.org/10.1055/s-0037-1609756
https://doi.org/10.1055/s-0037-1609756
Autor:
Angelo C. Pinto, Fernando de C. da Silva, Vitor F. Ferreira, Dora C. S. Costa, Mariana F. C. Cardoso, Luana da S. M. Forezi, R. Ribeiro
Publikováno v:
Revista Virtual de Química. 9:974-1064
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f88148766e55570ef900b887973ea692
https://doi.org/10.21577/1984-6835.20170063
https://doi.org/10.21577/1984-6835.20170063
Autor:
Maria Francilene Souza Silva, Vitor F. Ferreira, Claudia Pessoa, Andre Felippe de Almeida Xavier, Yen G. de Paiva, Mariana F. C. Cardoso, Marília O. F. Goulart, Daniel Pascoalino Pinheiro, Fernando de C. da Silva, Thaissa L. Silva
Publikováno v:
Journal of the Brazilian Chemical Society. 30
Electrochemical methods are powerful in the characterization and design of redox-modulating agents. We, herein, report the electrochemical investigation, in aprotic medium, of eleven synthetic 3-thio-substituted-nor-beta-lapachones, along with the de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90c898a54be2a19473584542f40d075d
https://doi.org/10.21577/0103-5053.20180248
https://doi.org/10.21577/0103-5053.20180248
Autor:
Ângelo C. Pinto, Maria G. P. M. S. Neves, Mariana F. C. Cardoso, Luana da S. M. Forezi, José A. S. Cavaleiro, Vitor F. Ferreira, Fernando de C. da Silva
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 20:167-189
This review focuses on synthetic strategies that have been established for the preparation of porphyrin-quinone conjugates of potential biological significance and as donor–acceptor compounds for electron transfer processes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44ba1b7218fb6488119643e4470946f4
https://doi.org/10.1142/s1088424616300093
https://doi.org/10.1142/s1088424616300093