Zobrazeno 1 - 9
of 9
pro vyhledávání: '"L. F. Bispo"'
Autor:
L. F. Bispo, G. L. Demolin-Leite, W. M. Fagundes, A. M. S. A. Abreu, J. M. M. dos Santos, F. M. M. Oliveira, V. J. Silva, T. O. Souza, Y. O. R. Silva, F. L. Amaral
Publikováno v:
Brazilian Journal of Biology, Vol 83 (2023)
Externí odkaz:
https://doaj.org/article/9432b5025daf429cbb6baf4d654d52e0
Autor:
Dário Silva, Márcio V. C. Lopes, Željko Petrovski, Miguel M. Santos, Jussevania P. Santos, Sueli F. Yamada-Ogatta, Marcelle L. F. Bispo, Marcus V. N. de Souza, Ana Rita C. Duarte, Maria C. S. Lourenço, Raoni Schroeder B. Gonçalves, Luis C. Branco
Publikováno v:
Molecules, Vol 27, Iss 16, p 5167 (2022)
The development of novel pharmaceutical tools to efficiently tackle tuberculosis is the order of the day due to the rapid development of resistant strains of Mycobacterium tuberculosis. Herein, we report novel potential formulations of a repurposed d
Externí odkaz:
https://doaj.org/article/a6a4378ca57e49f6ae1230e45fe18e10
Autor:
Jéseka G. Schirmann, Bruna T. S. Bortoleti, Manoela D. Gonçalves, Fernanda Tomiotto-Pellissier, Priscila G. Camargo, Milena M. Miranda-Sapla, Camilo H. S. Lima, Marcelle L. F. Bispo, Idessania N. Costa, Ivete Conchon-Costa, Wander R. Pavanelli, Robert F. H. Dekker, Aneli M. Barbosa-Dekker
Publikováno v:
Scientific Reports. 13
Available treatments for leishmaniasis have been widely used since the 1940s but come at a high cost, variable efficacy, high toxicity, and adverse side-effects. 3,3′,5,5′-Tetramethoxy-biphenyl-4,4′-diol (TMBP) was synthesized through laccase-c
Publikováno v:
Revista Virtual de Química.
Autor:
Renata P. Biasi‐Garbin, Marciéli Fabris, Ana Elisa B. Morguette, Gabriella M. Andriani, Weslei R. C. Cabral, Patrícia M. L. Pereira, Tiago O. Brito, Fernando Macedo, Camilo H. Da Silva Lima, César A. C. Lancheros, Celso V. Nakamura, Phileno Pinge‐Filho, Eliandro R. Tavares, Lucy M. Yamauchi, Marcelle L. F. Bispo, Sueli F. Yamada‐Ogatta
Publikováno v:
ChemistrySelect. 7
Autor:
Marcelle L. F. Bispo, Camilo H. S. Lima, Laura N. F. Cardoso, André L. P. Candéa, Flávio A. F. M. Bezerra, Maria C. S. Lourenço, Maria G. M. O. Henriques, Ricardo B. Alencastro, Carlos R. Kaiser, Marcus V. N. Souza, Magaly G. Albuquerque
Publikováno v:
Pharmaceuticals, Vol 10, Iss 2, p 52 (2017)
In an ongoing research program for the development of new anti-tuberculosis drugs, we synthesized three series (A, B, and C) of 7-chloro-4-aminoquinolines, which were evaluated in vitro against Mycobacterium tuberculosis (MTB). Now, we report the ant
Externí odkaz:
https://doaj.org/article/1bd0b3f01c1141e3a7d926e13ac67d2d
Publikováno v:
Revista Fitos. 5:53-63
No campo da descoberta de fármacos, o núcleo quinolínico é uma importante classe de compostos heterocíclicos, visto que está presente em muitos produtos naturais e sintéticos, os quais possuem um amplo espectro de atividades biológicas. Porta
Autor:
Laura N F, Cardoso, Marcelle L F, Bispo, Carlos R, Kaiser, James L, Wardell, Solange M S V, Wardell, Maria C S, Lourenço, Flávio A F M, Bezerra, Rodrigo P P, Soares, Marcele N, Rocha, Marcus V N, de Souza
Publikováno v:
Archiv der Pharmazie. 347(6)
A series of N-acylhydrazonyl-thienyl derivatives (compounds 2 and 3), mainly of the type 2-(aryl-CH=N-NHCOCH2 )-thiene (2: aryl = substituted-phenyl; 3: aryl = heteroaryl) were evaluated against Mycobacterium tuberculosis. Particularly active compoun
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