2015
DOI: 10.3109/14756366.2015.1010527
|View full text |Cite
|
Sign up to set email alerts
|

(7-Chloroquinolin-4-yl)arylhydrazones: Candida albicansenzymatic repression and cytotoxicity evaluation, Part 2

Abstract: These results revealed that select (7-chloroquinolin-4-yl)arylhydrazones may be potential antifungal agents for the control of C. albicans infections.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
4
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 8 publications
(4 citation statements)
references
References 29 publications
(49 reference statements)
0
4
0
Order By: Relevance
“…Moreover, industry has stimulated the development of new methods to identify and inhibit these virulence factors with lower doses of antimicrobials, aiming to avoid an increase in antifungal resistance [5].…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, industry has stimulated the development of new methods to identify and inhibit these virulence factors with lower doses of antimicrobials, aiming to avoid an increase in antifungal resistance [5].…”
Section: Introductionmentioning
confidence: 99%
“…The active derivatives showed MIC and MFC values in the range of 25 μg/ml and 50 μg/ml, which was the activity comparable with the fluconazole. Four of these hydrazones potently inhibited enzymatic processes in C. albicans at sub-antifungal concentrations, showing enzymatic repression of phospholipase and aspartyl proteases, which are the most frequent enzymes produced by C. albicans (de Azambuja Carvalho et al 2016). Notably, the compounds exhibited low cytotoxicity against mouse fibroblasts (NIH/3 T3 cell line) at sub-antifungal concentrations.…”
Section: Antifungal Activitymentioning
confidence: 99%
“…7-Chloroquinoline hydrazones have been previously developed and successfully tested in vitro for many biological activities [ 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 , 33 ]. The major part of the studies has been carried out to identify their antimalarial properties [ 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 ].…”
Section: Introductionmentioning
confidence: 99%
“…The major part of the studies has been carried out to identify their antimalarial properties [ 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 ]. In addition, these hydrazones were explored for their anti-leishmanial [ 10 , 11 , 12 , 13 ], anti-tubercular [ 3 , 14 , 15 , 16 , 17 , 18 ], anti-bacterial [ 19 , 20 ], anti-oxidant [ 21 , 22 ], anti-fungal [ 23 , 24 ], anti-viral [ 25 ], anti-inflammatory [ 26 ], anti-prion disease [ 27 ], anti-convulsant [ 28 ], antinociceptive [ 29 ], but also anticancer activities [ 30 , 31 , 32 , 33 ]. Many chemical modulations have been realized on 7-chloroquinoline hydrazones.…”
Section: Introductionmentioning
confidence: 99%