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In humans, metabolism of many drugs is carried out by CYP3A, whereas in rats and dogs, CYP2C is a primary drug metabolism enzyme, as CYP3A levels in rats and dogs only reaches half the levels of their CYP2C activity

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N-Acetyl Semax Amidate is characterized by the integration of acetic acid at the N-terminus and amidation at the C-terminus, which have been shown to confer additional advantages, such as fortifying the N-terminus and C-terminus against leucine aminopeptidase-mediated degradation and hydrolysis [6, 7]

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