Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Natália V. Barbosa"'
Autor:
Diego B. Carvalho, Amarith R. das Neves, Natália V. Barbosa, Antonio M. Honorato, Nidia C. Yoshida, Ozildéia S. Trefzger, Adriano C. M. Baroni, Carla Cardozo Pinto de Arruda, Iluska Senna Bonfá Moslaves, Mônica Cristina Toffoli Kadri, Massuo J. Kato
Publikováno v:
Chemical Biology & Drug Design. 94:2004-2012
Isoxazole analogues derived from the neolignans veraguensin, grandisin, and machilin G were previously synthesized with different substitution patterns through the bioisosterism strategy. These compounds were tested on intracellular amastigotes of Le
Autor:
Amarith R, das Neves, Ozildéia S, Trefzger, Natália V, Barbosa, Antonio M, Honorato, Diego B, Carvalho, Iluska S, Moslaves, Mônica C T, Kadri, Nidia C, Yoshida, Massuo J, Kato, Carla C P, Arruda, Adriano C M, Baroni
Publikováno v:
Chemical biologydrug designREFERENCES. 94(6)
Isoxazole analogues derived from the neolignans veraguensin, grandisin, and machilin G were previously synthesized with different substitution patterns through the bioisosterism strategy. These compounds were tested on intracellular amastigotes of Le
Autor:
Natália V. Barbosa, Ozildéia S. Trefzger, Renata Trentin Perdomo, Sérgio de Albuquerque, Maria de Fatima Cepa Matos, Carla Cardozo Pinto de Arruda, Amarith R. das Neves, Indiara Correia Pereira, Massuo J. Kato, Nidia C. Yoshida, Diego B. Carvalho, Adriano C. M. Baroni
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Using bioisosterism as a medicinal chemistry tool, 16 3,5-diaryl-isoxazole analogues of the tetrahydrofuran neolignans veraguensin, grandisin and machilin G were synthesized via 1,3-dipolar cycloaddition reactions, with yields from 43% to 90%. Antitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b4549abe2574c3ab0ac31b94dd69ff6