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In this review, we discuss the evolution in computational pharmacology as the next generation of successful drug discovery and implementation in the clinic where high-performance computing (HPC) is used to generate and validate drug-target-effect hypotheses completely in silico

Indeed, Grx1 and GSH receiving electrons from NADPH via glutathione reductase, could serve as alternative reducing agents of the disulphide in Trx1 active site (Cys32 and Cys35)

Future prospects include the integration of nanotechnology and targeted delivery platforms to enhance therapeutic efficacy and consumer acceptance

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