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In addition to preventing protein glycation, PLP is an effective inhibitor of lipid (fat) glycation (Higuchi 2006)

a corresponding pharmaceutically acceptable salt may be formed, e.g., by protonation of an atom carrying an electron lone pair which is susceptible to protonation, such as an amino group, with an inorganic or organic acid, or as a salt of a carboxylic acid group with a physiologically acceptable cation as they are well-known in the art

The system will create a new one to use

Each GST isozyme has a positively charged substrate-binding pocket, divided into a GSH-binding site (G-site) and an adjacent hydrophobic co-substrate-binding site (H-site)

Condoliase for the Treatment of Lumbar Disc Herniation

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