In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction (2013)
- Authors:
- USP affiliated authors: PAULA, MURILO HELDER DE - FCFRP ; EMERY, FLAVIO DA SILVA - FCFRP
- Unidade: FCFRP
- DOI: 10.1016/j.bmcl.2013.06.033
- Subjects: ANTIPARASITÁRIOS; PLASMODIUM; PRODUTOS NATURAIS (FARMACOLOGIA)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Bioorganic and Medicinal Chemistry Letters
- ISSN: 0960-894X
- Volume/Número/Paginação/Ano: v. 23, n. 16, p. 4583-4586, 2013
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
REZENDE, Lucas Cunha Dias de et al. In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction. Bioorganic and Medicinal Chemistry Letters, v. 23, n. 16, p. 4583-4586, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2013.06.033. Acesso em: 12 maio 2024. -
APA
Rezende, L. C. D. de, Fumagalli, F., Bortolin, M. S., Oliveira, M. G. de, Paula, M. H. de, Andrade-Neto, V. F. de, & Emery, F. da S. (2013). In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction. Bioorganic and Medicinal Chemistry Letters, 23( 16), 4583-4586. doi:10.1016/j.bmcl.2013.06.033 -
NLM
Rezende LCD de, Fumagalli F, Bortolin MS, Oliveira MG de, Paula MH de, Andrade-Neto VF de, Emery F da S. In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction [Internet]. Bioorganic and Medicinal Chemistry Letters. 2013 ; 23( 16): 4583-4586.[citado 2024 maio 12 ] Available from: https://doi.org/10.1016/j.bmcl.2013.06.033 -
Vancouver
Rezende LCD de, Fumagalli F, Bortolin MS, Oliveira MG de, Paula MH de, Andrade-Neto VF de, Emery F da S. In vivo antimalarial activity of novel 2-hydroxy-3-anilino-1,4-naphthoquinones obtained by epoxide ring-opening reaction [Internet]. Bioorganic and Medicinal Chemistry Letters. 2013 ; 23( 16): 4583-4586.[citado 2024 maio 12 ] Available from: https://doi.org/10.1016/j.bmcl.2013.06.033 - Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid
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Informações sobre o DOI: 10.1016/j.bmcl.2013.06.033 (Fonte: oaDOI API)
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