2014
DOI: 10.1016/j.bmcl.2013.11.037
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Synthesis and evaluation of novel azoles as potent antifungal agents

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Cited by 26 publications
(12 citation statements)
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“…Azoles bind with a nitrogen atom to the iron atom of the heme, preventing the demethylation of lanosterol [6]. The depletion of ergosterol and accumulation of 14a-methylated sterols disrupt the structure and many functions of fungal membrane leading to inhibition of fungal growth [7].…”
Section: Introductionmentioning
confidence: 99%
“…Azoles bind with a nitrogen atom to the iron atom of the heme, preventing the demethylation of lanosterol [6]. The depletion of ergosterol and accumulation of 14a-methylated sterols disrupt the structure and many functions of fungal membrane leading to inhibition of fungal growth [7].…”
Section: Introductionmentioning
confidence: 99%
“…In order to combat these infections, a number of antifungal agents are clinically available [195]. Emergence of resistance to the available drugs is a great encumbrance in the treatment of fungal infections and hence, development of new antifungal agents in a never ending task for chemists [196]. Over the time, numerous antifungal agents bearing piperazine have been developed by researchers (Figure 7).…”
Section: Antifungal Activitymentioning
confidence: 99%
“…The high resistance to azoles that was observed is worrisome. Due to their broad spectrum of activity and safety profiles, azoles are the most commonly used antifungal drugs (Li et al, 2014).…”
Section: Antifungal Susceptibility Patternmentioning
confidence: 99%