Antimicrobial activity of allylic thiocyanates derived from the Morita-Baylis-Hillman reaction.

Braz J Microbiol

Departamento de Engenharia Química Universidade Tecnológica Federal do Paraná Ponta GrossaPR Brazil Departamento de Engenharia Química, Universidade Tecnológica Federal do Paraná, Ponta Grossa, PR, Brazil.

Published: July 2015

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204962PMC
http://dx.doi.org/10.1590/s1517-83822014000300007DOI Listing

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