Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives
<div>In attempt to find new pharmacologically active molecules, we report here the synthesis and in vitro antimicrobial activities of various novel 1,3,4-oxadiazole containing 5-phenyltetrazole. The Schiff bases were obtained by condensation 2-(5-phenyl-1H-tetrazol-1-yl)acetohydrazide...
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Universidade Federal de Mato Grosso do Sul
2011-09-01
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doaj-53aadc09a789477692f3bbad196e031c2021-07-07T19:22:33ZengUniversidade Federal de Mato Grosso do SulOrbital: The Electronic Journal of Chemistry1984-64282011-09-013211712410.17807/orbital.v3i2.22586Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivativesPopat B. Mohite0V. H. Bhaskar1Department of Pharmaceutical Chemistry, MES College of Pharmacy, Sonai, AhmednagarMP Patel College of Pharmacy, Kapadwanj, Gujrat<div>In attempt to find new pharmacologically active molecules, we report here the synthesis and in vitro antimicrobial activities of various novel 1,3,4-oxadiazole containing 5-phenyltetrazole. The Schiff bases were obtained by condensation 2-(5-phenyl-1H-tetrazol-1-yl)acetohydrazide with various aromatic aldehydes. Cyclocondensation of Schiff’s bases with acetic anhydride results in 1,3,4-oxadiazole derivatives. The structures of the newly synthesized 1,3,4-oxadiazole were confirmed by FT-IR, 1H NMR and mass spectral data. The antimicrobial activity was determined by MIC method. All the compounds exhibited weak to potent antimicrobial activity. Some derivatives bearing a methoxy group exhibited very good antimicrobial activity at conc. of 62.5 µg/mL.</div>http://orbital.ufms.br/index.php/Chemistry/article/view/2251,3,4-oxadiazoletetrazoleantimicrobial activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Popat B. Mohite V. H. Bhaskar |
spellingShingle |
Popat B. Mohite V. H. Bhaskar Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives Orbital: The Electronic Journal of Chemistry 1,3,4-oxadiazole tetrazole antimicrobial activity |
author_facet |
Popat B. Mohite V. H. Bhaskar |
author_sort |
Popat B. Mohite |
title |
Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives |
title_short |
Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives |
title_full |
Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives |
title_fullStr |
Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives |
title_full_unstemmed |
Synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives |
title_sort |
synthesis and evaluation of antimicrobial activity of novel 1,3,4-oxadiazole derivatives |
publisher |
Universidade Federal de Mato Grosso do Sul |
series |
Orbital: The Electronic Journal of Chemistry |
issn |
1984-6428 |
publishDate |
2011-09-01 |
description |
<div>In attempt to find new pharmacologically active molecules, we report here the synthesis and in vitro antimicrobial activities of various novel 1,3,4-oxadiazole containing 5-phenyltetrazole. The Schiff bases were obtained by condensation 2-(5-phenyl-1H-tetrazol-1-yl)acetohydrazide with various aromatic aldehydes. Cyclocondensation of Schiff’s bases with acetic anhydride results in 1,3,4-oxadiazole derivatives. The structures of the newly synthesized 1,3,4-oxadiazole were confirmed by FT-IR, 1H NMR and mass spectral data. The antimicrobial activity was determined by MIC method. All the compounds exhibited weak to potent antimicrobial activity. Some derivatives bearing a methoxy group exhibited very good antimicrobial activity at conc. of 62.5 µg/mL.</div> |
topic |
1,3,4-oxadiazole tetrazole antimicrobial activity |
url |
http://orbital.ufms.br/index.php/Chemistry/article/view/225 |
work_keys_str_mv |
AT popatbmohite synthesisandevaluationofantimicrobialactivityofnovel134oxadiazolederivatives AT vhbhaskar synthesisandevaluationofantimicrobialactivityofnovel134oxadiazolederivatives |
_version_ |
1721314869911748608 |