Source: Chemical Biology and Drug Design. Unidades: IQ, FCFRP
Subjects: FITOQUÍMICA, ANTIPROTOZOÁRIOS
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TREFZGER, Ozildeia S et al. Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G. Chemical Biology and Drug Design, v. 93, n. 3, p. 313-324, 2019Tradução . . Disponível em: https://doi.org/10.1111/cbdd.13417. Acesso em: 16 maio 2024.APA
Trefzger, O. S., Neves, A. R. das, Barbosa, N. V., Carvalho, D. B., Pereira, I. C., Perdomo, R. T., et al. (2019). Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G. Chemical Biology and Drug Design, 93( 3), 313-324. doi:10.1111/cbdd.13417NLM
Trefzger OS, Neves AR das, Barbosa NV, Carvalho DB, Pereira IC, Perdomo RT, Matos MFC, Yoshida NC, Kato MJ, Albuquerque S de, Arruda CCP, Baroni ACM. Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G [Internet]. Chemical Biology and Drug Design. 2019 ; 93( 3): 313-324.[citado 2024 maio 16 ] Available from: https://doi.org/10.1111/cbdd.13417Vancouver
Trefzger OS, Neves AR das, Barbosa NV, Carvalho DB, Pereira IC, Perdomo RT, Matos MFC, Yoshida NC, Kato MJ, Albuquerque S de, Arruda CCP, Baroni ACM. Design, synthesis and antitrypanosomatid activities of 3,5-diaryl-isoxazole analogues based on neolignans veraguensin, grandisin and machilin G [Internet]. Chemical Biology and Drug Design. 2019 ; 93( 3): 313-324.[citado 2024 maio 16 ] Available from: https://doi.org/10.1111/cbdd.13417