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: 11 nov. 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 nov. 11 ] 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 nov. 11 ] Available from: https://doi.org/10.1111/cbdd.13417