SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETY
ABSTRACT Three new Schiff bases bearing benzimidazole and p-toluen sulfonamide moiety were synthesized. Their structures were characterized by elemental analysis, FTIR, NMR and LCMS methods. The antimicrobial properties of the compounds were also evaluated. All compounds exhibit higher antimicrobial...
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Sociedad Chilena de Química
2019
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oai:scielo:S0717-970720190004045902020-02-03SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETYTunc,Turgay Benzimidazole Schiff bases antimicrobial activity ABSTRACT Three new Schiff bases bearing benzimidazole and p-toluen sulfonamide moiety were synthesized. Their structures were characterized by elemental analysis, FTIR, NMR and LCMS methods. The antimicrobial properties of the compounds were also evaluated. All compounds exhibit higher antimicrobial activity against all bacteria, Schiff bases (4a-4c) shows more activity than the parent aldehyde (3). 4c displays higher antibacterial activity against P. aeruginosa compare to reference drug Sulfioxazole. The compounds were found more potent against Gram-negative than Gram positive bacteria. One more free phenyl group increase the activity in 4c, but one more phenyl ring in 4b does not. In vitro antifungal activity of the compounds was also tested on fungi C. albicans C. tropicalis and C. krusei. However, our compounds exhibit no antifungal activity against three fungi.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.64 n.4 20192019-12-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072019000404590en10.4067/S0717-97072019000404590 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
English |
topic |
Benzimidazole Schiff bases antimicrobial activity |
spellingShingle |
Benzimidazole Schiff bases antimicrobial activity Tunc,Turgay SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETY |
description |
ABSTRACT Three new Schiff bases bearing benzimidazole and p-toluen sulfonamide moiety were synthesized. Their structures were characterized by elemental analysis, FTIR, NMR and LCMS methods. The antimicrobial properties of the compounds were also evaluated. All compounds exhibit higher antimicrobial activity against all bacteria, Schiff bases (4a-4c) shows more activity than the parent aldehyde (3). 4c displays higher antibacterial activity against P. aeruginosa compare to reference drug Sulfioxazole. The compounds were found more potent against Gram-negative than Gram positive bacteria. One more free phenyl group increase the activity in 4c, but one more phenyl ring in 4b does not. In vitro antifungal activity of the compounds was also tested on fungi C. albicans C. tropicalis and C. krusei. However, our compounds exhibit no antifungal activity against three fungi. |
author |
Tunc,Turgay |
author_facet |
Tunc,Turgay |
author_sort |
Tunc,Turgay |
title |
SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETY |
title_short |
SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETY |
title_full |
SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETY |
title_fullStr |
SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETY |
title_full_unstemmed |
SYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETY |
title_sort |
synthesis and antimicrobial study of new benzimidazole schiff bases bearing p-toluene sulfonamide moiety |
publisher |
Sociedad Chilena de Química |
publishDate |
2019 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072019000404590 |
work_keys_str_mv |
AT tuncturgay synthesisandantimicrobialstudyofnewbenzimidazoleschiffbasesbearingptoluenesulfonamidemoiety |
_version_ |
1714200942109261824 |