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Fatty acid + ATP + CoA Acyl-CoA + PP i + AMP Table of the Mammalian Acyl-CoA Synthetase Family Fatty Acid Deactivation Once a fatty acid is esterified to coenzyme A forming an acyl-CoA, its fate is not destined for oxidation in the mitochondria or the peroxisomes

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Considering that many chronic age-related diseases appear to have some degree of mitochondrial dysfunction as part of their etiology, it is notable that alterations in mGSH homeostasis may be a central factor in this dysfunction

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