Neuropeptide Y

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G8165 Galanin (1-13)-Neuropeptide Y (25-36) Amide ≥90% This chimeric peptide is a high affinity galanin receptor antagonist (IC50=0.1 nM in rat hypothalamus membranes and Kd=0.01 nm in rat spinal cord membranes). This peptide is also recognized by neuropeptide Y receptors (IC50=0.25 μM in rat cerebral cortex membranes) and is a Y2 agonist in rat vas deferens.
N8648 GR 231118 ≥95% (HPLC), lyophilized powder High affinity and selective NPY Y1 receptor antagonist.
N9398 N-Acetyl-[Leu28, Leu31]-Neuropeptide Y Fragment 24-36 ≥98% (HPLC), powder N-Acetyl-[Leu28, Leu31]-Neuropeptide Y Fragment 24-36 is a neuropeptide Y-Y2 receptor agonist.
Selective neuropeptide Y-Y2 receptor agonist.
N5017 Neuropeptide Y human ≥95% (HPLC), powder, synthetic Vasoconstrictor; brain peptide that inhibits Ca2+-activated K+ channels in vascular smooth muscle. Implicated in the control of blood pressure, sexual behavior and food intake. Inhibits cholecystokinin- and secretin-stimulated pancreatic secretion.
N8154 [Ala31, α-Aminoisobutyryl32]-Neuropeptide Y porcine ≥98% (HPLC), solid Agonist for the neuropeptide Y5 receptor exhibiting high affinity and selectivity.
N3266 Neuropeptide Y porcine ≥97% (HPLC), synthetic Vasoconstrictor; brain peptide that inhibits Ca2+-activated K+ channels in vascular smooth muscle. Implicated in the control of blood pressure, sexual behavior and food intake. Inhibits cholecystokinin- and secretin-stimulated pancreatic secretion.
N9407 Neuropeptide Y Fragment 3-36 human, rat ≥95% (HPLC) Endogenous neuropeptide that selectively binds to Y2 and Y5 receptors.
N1272 Neuropeptide Y Fragment 18-36 human, porcine A competitive NPY antagonist in cardiac membranes
N6521 Neuropeptide Y Fragment 13-36 porcine ≥97% (HPLC) Selective neuropeptide Y2 receptor agonist.
N5771 [O-Methyl-Tyr21]-Neuropeptide Y human ≥97% (HPLC) [O-Methyl-Tyr21]-Neuropeptide Y human is a Neuropeptide Y analog with a high affinity for brain receptors.
N6269 Neuropeptide Y sheep ≥97% (HPLC), synthetic Vasoconstrictor; brain peptide that inhibits Ca2+-activated K+ channels in vascular smooth muscle. Implicated in the control of blood pressure, sexual behavior and food intake. Inhibits cholecystokinin- and secretin-stimulated pancreatic secretion.