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Andreassen and colleagues (J Med Chem, 2021) reported a design campaign that combined sequence substitutions to suppress fibrillation with a fatty-acid acylation that promotes albumin binding, yielding a molecule with a much longer reported plasma half-life in their preclinical models

These findings correspond to the influence of NL-Epitalon on various stress-induced changes in nSMase activity in the P2 fraction of the cerebral cortex