A neurotensin-like octapeptide
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Xenopsin is a neurotensin-like octapeptide that has been found in X. laevis skin.1 It inhibits neurotensin binding to rat brain synaptic membranes (Ki = 1.5 nM) and induces contraction of isolated guinea pig ileum in the presence of neostigmine .2 Xenopsin (0.1 μM) increases the firing rate of dopaminergic neurons in rat substantia nigra slices by 58.5%.3 Intravenous infusion of xenopsin (2 μg/kg per hour) increases adrenal, pancreatic, and ileal blood flow and plasma levels of pancreatic polypeptide, glucagon, substance P, and cortisol, as well as reduces tetragastrin-induced gastric acid secretion in dogs.1
1.Zinner, M.J., Kasher, F., Modlin, I.M., et al.Effect of xenopsin on blood flow, hormone release, and acid secretionAm. J. Physiol.243(3)G195-199(1982) 2.Granier, C., van Rietschoten, J., Kitabgi, P., et al.Synthesis and characterization of neurotensin analogues for structure/activity relationship studies. Acetyl-neurotensin-(8--13) is the shortest analogue with full binding and pharmacological activitiesEur. J. Biochem.124(1)117-124(1982) 3.Pozza, M.F., Küng, E., Bischoff, S., et al.The neurotensin analog xenopsin excites nigral dopamine neuronsEur. J. Pharmacol.145(3)341-343(1988)
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