7-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal Activity

Fifteen 7-chloro-4-arylhydrazonequinolines have been evaluated for their in vitro antifungal activity against eight oral fungi: Candida albicans, C. parapsilosis, C. lipolytica, C. tropicalis, C. famata, C. glabrata, Rhodutorula mucilaginosa, and R. glutinis. Several compounds exhibited minimum inhi...

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Main Authors: Auri R. Duval, Pedro H. Carvalho, Maieli C. Soares, Daniela P. Gouvêa, Geonir M. Siqueira, Rafael G. Lund, Wilson Cunico
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2011.141
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author Auri R. Duval
Pedro H. Carvalho
Maieli C. Soares
Daniela P. Gouvêa
Geonir M. Siqueira
Rafael G. Lund
Wilson Cunico
author_facet Auri R. Duval
Pedro H. Carvalho
Maieli C. Soares
Daniela P. Gouvêa
Geonir M. Siqueira
Rafael G. Lund
Wilson Cunico
author_sort Auri R. Duval
collection DOAJ
description Fifteen 7-chloro-4-arylhydrazonequinolines have been evaluated for their in vitro antifungal activity against eight oral fungi: Candida albicans, C. parapsilosis, C. lipolytica, C. tropicalis, C. famata, C. glabrata, Rhodutorula mucilaginosa, and R. glutinis. Several compounds exhibited minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) activities comparable with the first-line drug fluconazole. These results could be considered as an important starting point for the rational design of new antifungal agents.
format Article
id doaj-art-8afd6c2cb12a445b99ee5b089b2ebd1c
institution Kabale University
issn 1537-744X
language English
publishDate 2011-01-01
publisher Wiley
record_format Article
series The Scientific World Journal
spelling doaj-art-8afd6c2cb12a445b99ee5b089b2ebd1c2025-02-03T06:14:12ZengWileyThe Scientific World Journal1537-744X2011-01-01111489149510.1100/tsw.2011.1417-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal ActivityAuri R. Duval0Pedro H. Carvalho1Maieli C. Soares2Daniela P. Gouvêa3Geonir M. Siqueira4Rafael G. Lund5Wilson Cunico6NuQuiA—Núcleo de Química Aplicada, Centro de Ciências Químicas, Farmacêuticas e de Alimentos (CCQFA), Universidade Federal de Pelotas, Campus Universitário, Pelotas, RS, BrazilLaboratório de Microbiologia Oral, Faculdade de Odontologia, Universidade Federal de Pelotas, Pelotas, RS, BrazilNuQuiA—Núcleo de Química Aplicada, Centro de Ciências Químicas, Farmacêuticas e de Alimentos (CCQFA), Universidade Federal de Pelotas, Campus Universitário, Pelotas, RS, BrazilNuQuiA—Núcleo de Química Aplicada, Centro de Ciências Químicas, Farmacêuticas e de Alimentos (CCQFA), Universidade Federal de Pelotas, Campus Universitário, Pelotas, RS, BrazilNuQuiA—Núcleo de Química Aplicada, Centro de Ciências Químicas, Farmacêuticas e de Alimentos (CCQFA), Universidade Federal de Pelotas, Campus Universitário, Pelotas, RS, BrazilLaboratório de Microbiologia Oral, Faculdade de Odontologia, Universidade Federal de Pelotas, Pelotas, RS, BrazilNuQuiA—Núcleo de Química Aplicada, Centro de Ciências Químicas, Farmacêuticas e de Alimentos (CCQFA), Universidade Federal de Pelotas, Campus Universitário, Pelotas, RS, BrazilFifteen 7-chloro-4-arylhydrazonequinolines have been evaluated for their in vitro antifungal activity against eight oral fungi: Candida albicans, C. parapsilosis, C. lipolytica, C. tropicalis, C. famata, C. glabrata, Rhodutorula mucilaginosa, and R. glutinis. Several compounds exhibited minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) activities comparable with the first-line drug fluconazole. These results could be considered as an important starting point for the rational design of new antifungal agents.http://dx.doi.org/10.1100/tsw.2011.141
spellingShingle Auri R. Duval
Pedro H. Carvalho
Maieli C. Soares
Daniela P. Gouvêa
Geonir M. Siqueira
Rafael G. Lund
Wilson Cunico
7-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal Activity
The Scientific World Journal
title 7-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal Activity
title_full 7-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal Activity
title_fullStr 7-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal Activity
title_full_unstemmed 7-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal Activity
title_short 7-Chloroquinolin-4-yl Arylhydrazone Derivatives: Synthesis and Antifungal Activity
title_sort 7 chloroquinolin 4 yl arylhydrazone derivatives synthesis and antifungal activity
url http://dx.doi.org/10.1100/tsw.2011.141
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