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Examples of some of the more potent CYP 3A4 inhibitors include: antifungals ketoconazole and itraconazole, the protease inhibitors ritonavir, nelfinavir, and indinavir, and macrolide antibiotics erythromycin, clarithromycin, and troleandomycin

These compounds help neutralize free radicals, which are harmful molecules that cause oxidative stress and contribute to the aging process

Glucose-6-phosphate dehydrogenase deficiency and type 2 diabetes

The mechanism by which CGI1746 inhibited ferroptosis was found to be its chaperone, sigma-1R (1R), a receptor located on the mitochondrial membrane

Modulating locomotor adaptation with cerebellar stimulation