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Furan-containing thiacyanine analogs and their antimicrobial activity

  • I. Kortišová EMAIL logo , P. Foltínová and J. Halgaš
Published/Copyright: February 1, 2006
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Abstract

Condensation of quaternary 2-methylbenzothiazolium bromides with 5-(dialkylamino)furan-2-carbaldehydes afforded a series of new thiacyanine analogs. The compounds exhibit significant activities against several bacterial, yeast, and mould strains. Derivatives with dipropylamino substituents showed higher inhibitory effects than those with cyclic secondary amino groups. Hence, the biological activity may have been influenced by the lipophilicity of the compounds. The effect on growth and on the plastid system of the unicellular flagellate Euglena gracilis was also studied.

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Published Online: 2006-2-1
Published in Print: 2006-2-1

© 2006 Institute of Chemistry, Slovak Academy of Sciences

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