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Several small-molecule inhibitors of CYP51A1 have been developed, including clinically used azoles such as fluconazole and ketoconazole, which were originally designed to target fungal CYP51A1 but also inhibit the human enzyme (Table 3)

however, the expression of these genes was strongly downregulated following (h)GSH depletion (Figure 7)

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Two molecules of lactic acid contain exactly the same number of carbons, hydrogens, and oxygens as one molecule of glucose ( Fig