New antibacterial agents: hybrid bioisoster derivatives as potential E. coli FabH inhibitors (2016)
- Authors:
- USP affiliated authors: COELHO, FERNANDO RODRIGUES - IQ ; AUGUSTO, OHARA - IQ ; FERREIRA, ELIZABETH IGNE - FCF
- Unidades: IQ; FCF
- DOI: 10.1016/j.bmcl.2016.06.089
- Subjects: ANTIBIÓTICOS; ESCHERICHIA COLI
- Language: Inglês
- Imprenta:
- Source:
- Título: Bioorganic & Medicinal Chemistry Letters
- ISSN: 1061-9348
- Volume/Número/Paginação/Ano: v. 26, n. 16, p. 3988-3993, 2016
- Status:
- Artigo possui acesso gratuito no site do editor (Bronze Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
SEGRETTI, Natanael Dante et al. New antibacterial agents: hybrid bioisoster derivatives as potential E. coli FabH inhibitors. Bioorganic & Medicinal Chemistry Letters, v. 26, n. 16, p. 3988-3993, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2016.06.089. Acesso em: 01 abr. 2026. -
APA
Segretti, N. D., Serafim, R. A. M., Segretti, M. C. F., Miyata, M., Coelho, F. R., Augusto, O., & Ferreira, E. I. (2016). New antibacterial agents: hybrid bioisoster derivatives as potential E. coli FabH inhibitors. Bioorganic & Medicinal Chemistry Letters, 26( 16), 3988-3993. doi:10.1016/j.bmcl.2016.06.089 -
NLM
Segretti ND, Serafim RAM, Segretti MCF, Miyata M, Coelho FR, Augusto O, Ferreira EI. New antibacterial agents: hybrid bioisoster derivatives as potential E. coli FabH inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2016 ; 26( 16): 3988-3993.[citado 2026 abr. 01 ] Available from: https://doi.org/10.1016/j.bmcl.2016.06.089 -
Vancouver
Segretti ND, Serafim RAM, Segretti MCF, Miyata M, Coelho FR, Augusto O, Ferreira EI. New antibacterial agents: hybrid bioisoster derivatives as potential E. coli FabH inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2016 ; 26( 16): 3988-3993.[citado 2026 abr. 01 ] Available from: https://doi.org/10.1016/j.bmcl.2016.06.089 - Influence of quinoline - containig antimalarials in the catalase activity of ferriprotoporphyrin
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