Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Felipe R. C. Vicente"'
Autor:
Sílvia H. Cardoso, João Vítor de Assis, Mauro V. de Almeida, Maria Cristina S. Lourenço, Felipe R. C. Vicente, Marcus V. N. de Souza
Publikováno v:
Química Nova, Vol 32, Iss 6, Pp 1557-1560 (2009)
A series of 13 compounds analogous of isoniazid condensed with carbohydrate was synthesized and evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis H37Rv using Alamar Blue susceptibility test and the activity expres
Externí odkaz:
https://doaj.org/article/0323ab3a294f4f36a16d1006394b6db8
Autor:
João Vitor de Assis, Mauro V. de Almeida, Marcus V. N. de Souza, Maria C.S. Lourenço, Felipe R. C. Vicente, Sílvia Helena Cardoso
Publikováno v:
Química Nova, Vol 32, Iss 6, Pp 1557-1560 (2009)
Química Nova, Volume: 32, Issue: 6, Pages: 1557-1560, Published: 2009
Química Nova v.32 n.6 2009
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
Química Nova, Volume: 32, Issue: 6, Pages: 1557-1560, Published: 2009
Química Nova v.32 n.6 2009
Química Nova
Sociedade Brasileira de Química (SBQ)
instacron:SBQ
A series of 13 compounds analogous of isoniazid condensed with carbohydrate was synthesized and evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis H37Rv using Alamar Blue susceptibility test and the activity expres
Autor:
Monica Amado Peralta, Marcelle de Lima Ferreira, Felipe R. C. Vicente, Thais Cristina Mendonça Nogueira, Raoni S.B. Goncalves, Marcus V. N. de Souza, Maria C.S. Lourenço
Publikováno v:
Letters in Drug Design & Discovery. 5:221-224
Autor:
Marcus V. N. de Souza, Emerson T. da Silva, Raoni S.B. Goncalves, Felipe R. C. Vicente, Marcelle de Lima Ferreira, Maria C.S. Lourenço, Laura N. F. Cardoso
Publikováno v:
Letters in Drug Design & Discovery. 5:137-140
Autor:
Nádia R. Barbosa, Roberta C. N. Dos Reis, Maria C.S. Lourenço, Mireille Le Hyaric, Felipe R. C. Vicente, Simone C. Oda, Priscila Larcher Carneiro Santos, Mauro V. de Almeida, Rafael Trevizani
Publikováno v:
Repositório Institucional da UFJF
Universidade Federal de Juiz de Fora (UFJF)
instacron:UFJF
Universidade Federal de Juiz de Fora (UFJF)
instacron:UFJF
Diaminas N-monoalquiladas foram sintetizadas e tratadas com D-ribonolactona ou D-gliconolactona. As aldonamidas resultantes foram avaliadas para atividade antimicrobiana contra S. aureus, E. coli, M. tuberculosis and C. albicans. Duas hidrazidas fora
Autor:
Lívia L. Alves, Maria Aparecida de Souza, Mauro V. de Almeida, Maria C.S. Lourenço, Aline F. Taveira, Mireille Le Hyaric, Ana Paula Ferreira, Débora R. R. P. Araujo, Felipe R. C. Vicente, Elaine F. C. Reis
Publikováno v:
Bioorganic & Medicinal Chemistry. 15:7789-7794
A series of N- and C-alkylated amino alcohols and of their protected galactopyranosyl derivatives was synthesized and evaluated for antitubercular activity. Five of these compounds displayed good activity, with a MIC below 12.5mug/mL. The presence of
Autor:
Mauricio F. Saraiva, Felipe R. C. Vicente, Mauro V. de Almeida, Cristiane F. da Costa, Marcus V. N. de Souza, Maria C.S. Lourenço
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:5661-5664
Fluoroquinolone (FQ) has a broad spectrum of activity against several bacteria, mycobacteria, parasites, and other diseases. Moxifloxacin and gatifloxacin are a new generation of fluoroquinolone agents with improved activity against Gram-negative and
Autor:
Débora R. R. P. Araujo, Mauro V. De Almeida, Felipe R. C. Vicente, Cristiane F. da Costa, Mireille Le Hyaric, Celso O. R. Junior, Tais A. Correa, Maria C.S. Lourenço, Aline F. Taveira, Elaine F. C. Reis
Publikováno v:
ResearcherID
Memórias do Instituto Oswaldo Cruz., Vol 104, Iss 5, Pp 703-705 (2009)
Memórias do Instituto Oswaldo Cruz, Volume: 104, Issue: 5, Pages: 703-705, Published: AUG 2009
Memórias do Instituto Oswaldo Cruz., Vol 104, Iss 5, Pp 703-705 (2009)
Memórias do Instituto Oswaldo Cruz, Volume: 104, Issue: 5, Pages: 703-705, Published: AUG 2009
A series of diamines and amino alcohols derived from 1-dodecanol, 1-tetradecanol, 1,2-dodecanediol and 1,2-tetradecanediol were synthesized and tested for their antitubercular activity. Compounds 3, 8 and 9 were found to be the most active (MIC of 6.
Autor:
Felipe R. C. Vicente, Edson F. da Silva, Samir A. Carvalho, Marcus V. N. de Souza, Maria C.S. Lourenço
Publikováno v:
Bioorganicmedicinal chemistry letters. 18(2)
In this work, we report the synthesis and the antimycobacterial evaluation of new trans-cinnamic acid derivatives of isonicotinic acid series (5) and benzoic acid series (6), designed by exploring the molecular hybridization approach between isoniazi
Autor:
Raoni S.B. Goncalves, André L. P. Candéa, Maria C.S. Lourenço, Maria das Graças M. O. Henriques, Marcelle de Lima Ferreira, Marcus Vinícius Nora de Souza, Felipe R. C. Vicente, Thais Cristina Mendonça Nogueira
Publikováno v:
Bioorganicmedicinal chemistry letters. 17(24)
The present article describes a series of 21 N-(aryl)-2-thiophen-2-ylacetamides, which were synthesized and evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis, and the activity expressed as the minimum inhibitory c