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Merck
CN

Cyclic analogs of galanin and neuropeptide Y by hydrocarbon stapling.

Bioorganic & medicinal chemistry (2012-11-28)
Brad R Green, Brian D Klein, Hee-Kyoung Lee, Misty D Smith, H Steve White, Grzegorz Bulaj
摘要

Hydrocarbon stapling is an effective strategy to stabilize the helical conformation of bioactive peptides. Here we describe application of stapling to anticonvulsant neuropeptides, galanin (GAL) and neuropeptide Y (NPY), that are implicated in modulating seizures in the brain. Dicarba bridges were rationally introduced into minimized analogs of GAL and NPY resulting in increased α-helical content, in vitro metabolic stability and n-octanol/water partitioning coefficient (logD). The stapled analogs retained agonist activities towards their respective receptors and suppressed seizures in a mouse model of epilepsy.