Design, Synthesis, and Molecular Docking of 1-(1-(4-Chlorophenyl)-2-(phenylsulfonyl)ethylidene)-2-phenylhydrazine as Potent Nonazole Anticandidal Agent

<div>(a) Binding mode of fluconazole into the binding site cytochrome P450 14α-sterol demethylase. (b) Binding mode of<b> 13</b> into the binding site cytochrome P450 14α-sterol demethylase.</div>

Journal of Chemistry

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Figure 2

Figure 2: Design, Synthesis, and Molecular Docking of 1-(1-(4-Chlorophenyl)-2-(phenylsulfonyl)ethylidene)-2-phenylhydrazine as Potent Nonazole Anticandidal Agent 

Figure 2 | Design, Synthesis, and Molecular Docking of 1-(1-(4-Chlorophenyl)-2-(phenylsulfonyl)ethylidene)-2-phenylhydrazine as Potent Nonazole Anticandidal Agent 