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Design, synthesis and biological evaluation of glutathione peptidomimetics as components of anti-Parkinson prodrugs

Development and FDA Approval The development of Sermorelin arose from research in the 1970s-1980s that characterized GHRH structure, function, and identified that the biologically active portion responsible for GH-releasing activity resides in the N-terminal region of the molecule, specifically amino acids 1-29, while the C-terminal portion (amino acids 30-44) is not required for receptor binding or signaling

Walker, C

Due to the strong product inhibition in the GSH biosynthetic pathway, high levels of intracellular content, yield and productivity of GSH are difficult to achieve

We have observed a homeostatic imbalance of purine catabolism in first-episode neuroleptic-nave patients with SZ (FENNS)