SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVES

Some 4-[{1-(substituted)methylidine}-amino]-3-(4-pyridyl)-5-mercapto-4H-1,2,4-triazol (3a- 3f) and N-[5-(4-substituted)-1H-1,2,3-triazol-1-yl] isonicotinamide derivatives (5a- 5e) were synthesized by a sequence of reactions starting from isonicotinic acid hydrazide and is illustrated in scheme 1 and...

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Autores principales: MISHRA,RAVINESH, KUMAR,RAJIV, KUMAR,SURESH, MAJEED,JASEELA, RASHID,MOHD, SHARMA,SAMEER
Lenguaje:English
Publicado: Sociedad Chilena de Química 2010
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072010000300019
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spelling oai:scielo:S0717-970720100003000192011-01-25SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVESMISHRA,RAVINESHKUMAR,RAJIVKUMAR,SURESHMAJEED,JASEELARASHID,MOHDSHARMA,SAMEER Triazole derivatives Antimicrobial activity Ciprofloxacin Fluconazole Some 4-[{1-(substituted)methylidine}-amino]-3-(4-pyridyl)-5-mercapto-4H-1,2,4-triazol (3a- 3f) and N-[5-(4-substituted)-1H-1,2,3-triazol-1-yl] isonicotinamide derivatives (5a- 5e) were synthesized by a sequence of reactions starting from isonicotinic acid hydrazide and is illustrated in scheme 1 and 2. The antibacterial and antifungal activities of newly synthesized compounds were tested by the disc diffusion method using nutrient agar medium against various microorganisms such as gram positive Staphylococcus aureus and Bacillus subtilis, gram negative Escherichia coli and the fungi Aspergillus niger and Candida albicans. Ciprofloxacin and Fluconazole at 50 µg/mL were used as standard drugs for antibacterial and antifungal activities, respectively. All the synthesized compounds showed significant activity against various microorganisms.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.55 n.3 20102010-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072010000300019en10.4067/S0717-97072010000300019
institution Scielo Chile
collection Scielo Chile
language English
topic Triazole derivatives
Antimicrobial activity
Ciprofloxacin
Fluconazole
spellingShingle Triazole derivatives
Antimicrobial activity
Ciprofloxacin
Fluconazole
MISHRA,RAVINESH
KUMAR,RAJIV
KUMAR,SURESH
MAJEED,JASEELA
RASHID,MOHD
SHARMA,SAMEER
SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVES
description Some 4-[{1-(substituted)methylidine}-amino]-3-(4-pyridyl)-5-mercapto-4H-1,2,4-triazol (3a- 3f) and N-[5-(4-substituted)-1H-1,2,3-triazol-1-yl] isonicotinamide derivatives (5a- 5e) were synthesized by a sequence of reactions starting from isonicotinic acid hydrazide and is illustrated in scheme 1 and 2. The antibacterial and antifungal activities of newly synthesized compounds were tested by the disc diffusion method using nutrient agar medium against various microorganisms such as gram positive Staphylococcus aureus and Bacillus subtilis, gram negative Escherichia coli and the fungi Aspergillus niger and Candida albicans. Ciprofloxacin and Fluconazole at 50 µg/mL were used as standard drugs for antibacterial and antifungal activities, respectively. All the synthesized compounds showed significant activity against various microorganisms.
author MISHRA,RAVINESH
KUMAR,RAJIV
KUMAR,SURESH
MAJEED,JASEELA
RASHID,MOHD
SHARMA,SAMEER
author_facet MISHRA,RAVINESH
KUMAR,RAJIV
KUMAR,SURESH
MAJEED,JASEELA
RASHID,MOHD
SHARMA,SAMEER
author_sort MISHRA,RAVINESH
title SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVES
title_short SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVES
title_full SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVES
title_fullStr SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVES
title_full_unstemmed SYNTHESIS AND In vitro ANTIMICROBIAL ACTIVITY OF SOME TRIAZOLE DERIVATIVES
title_sort synthesis and in vitro antimicrobial activity of some triazole derivatives
publisher Sociedad Chilena de Química
publishDate 2010
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072010000300019
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AT kumarrajiv synthesisandinvitroantimicrobialactivityofsometriazolederivatives
AT kumarsuresh synthesisandinvitroantimicrobialactivityofsometriazolederivatives
AT majeedjaseela synthesisandinvitroantimicrobialactivityofsometriazolederivatives
AT rashidmohd synthesisandinvitroantimicrobialactivityofsometriazolederivatives
AT sharmasameer synthesisandinvitroantimicrobialactivityofsometriazolederivatives
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