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Urocortin-2 analogs are synthetic or modified versions of urocortin-2 (UCN2), a 38-amino acid peptide and selective agonist for the corticotropin-releasing factor type 2 receptor (CRF2). These analogs are designed to mimic or enhance the biological activity of native UCN2, often with improved pharmacokinetic properties. They are being explored for therapeutic applications including obesity, heart failure and muscle wasting disorders.
Selective agonism of the corticotropin-releasing factor type 2 receptor (CRHR2), leading to activation of the cAMP/PKA signaling pathway, Akt, and ERK1/ERK2 pathways.
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