Antimicrobial activity of allylic thiocyanates derived from the Morita-Baylis-Hillman reaction
Braz. j. microbiol
;
45(3): 807-812, July-Sept. 2014. ilus, tab
Artículo
en Inglés
| LILACS
| ID: lil-727006
ABSTRACT
Bacterial resistance to commonly used antibiotics has been recognized as a significant global health issue. In this study, we carried out the screening of a family of allylic thiocyanates for their action against a diversity of bacteria and fungi with a view to developing new antimicrobial agents. Allylic thiocyanates bearing halogenated aryl groups, which were readily obtained in two steps from the Morita-Baylis-Hillman adducts, showed moderate-to-high activity against selective pathogens, including a methicillin-resistant S. aureus (MRSA) strain. In particular cases, methyl (Z)-3-(2,4-dichlorophenyl)-2-(thiocyanomethyl)-2-propenoate exhibited antimicrobial activity comparable to the reference antibiotic Imipenem.
Texto completo:
Disponible
Índice:
LILACS (Américas)
Asunto principal:
Tiocianatos
/
Bacterias
/
Compuestos Alílicos
/
Hongos
/
Antiinfecciosos
Idioma:
Inglés
Revista:
Braz. j. microbiol
Asunto de la revista:
Microbiologia
Año:
2014
Tipo del documento:
Artículo
País de afiliación:
Brasil
Institución/País de afiliación:
Universidade Federal de Santa Catarina/BR
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