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Paltusotine is a nonpeptide somatostatin receptor 2 (SST2) agonist.1 It selectively inhibits cAMP production in cells expressing SST2 over cells expressing SST1, SST3, SST4, or SST5 (EC50s = 25, >1,000, >1,000, >1,000, and >1,000 nM, respectively). In vivo, paltusotine (3, 10, and 30 mg/kg) reduces growth hormone release stimulated by growth hormone-releasing hormone (GHRH) in rats. It also reduces plasma levels of insulin-like growth factor 1 (IGF-1) in beagle dogs.
WARNING This product is not for human or veterinary use.
1. Discovery of paltusotine (CRN00808), a potent, selective, and orally bioavailable non-