Nanjing Peptide Biotech Ltd
China
Product Name: h-tyr-pro-ser-lys-pro-asp-asn-pro-gly-glu-asp-ala-pro-ala-glu-asp-met-ala-arg-tyr-tyr-ser-ala-leu-nh2
Price: ￥Inquiry/10g ￥Inquiry/100g ￥Inquiry/1kg ￥Inquiry/10kg
Purity: 98.0%
Stocking Period: 7 Day
Contact: jom

131448-51-6

131448-51-6 structure

Name: Neuropeptide Y (1-24) amide (human, rat) trifluoroacetate salt
Chemical Name: h-tyr-pro-ser-lys-pro-asp-asn-pro-gly-glu-asp-ala-pro-ala-glu-asp-met-ala-arg-tyr-tyr-ser-ala-leu-nh2
CAS Number: 131448-51-6
Molecular Formula: C₁₁₆H₁₇₀N₃₀O₄₀S
Molecular Weight: 2656.83000
Catalog: Signaling Pathways GPCR/G Protein Neuropeptide Y Receptor
Create Date: 2018-12-19 14:14:29
Modify Date: 2024-02-02 18:39:40
Neuropeptide Y (1-24) (human) is a neuropeptide with potencies in inhibiting the electricity stimulated twitch response of rat vas deferens. Neuropeptide Y (1-24) (human) stimulates N-methyl-D-aspartate (NMDA)-induced neuronal activation in the rat CA3 region of the dorsal hippocampus in vivo[1][2].

Name	h-tyr-pro-ser-lys-pro-asp-asn-pro-gly-glu-asp-ala-pro-ala-glu-asp-met-ala-arg-tyr-tyr-ser-ala-leu-nh2
Synonyms	NEUROPEPTIDE Y FRAGMENT 1-24 AMIDE HUMAN npy 1-24 Neuropeptide Y Fragment 1-24 Amide human TYR-PRO-SER-LYS-PRO-ASP-ASN-PRO-GLY-GLU-ASP-ALA-PRO-ALA-GLU-ASP-MET-ALA-ARG-TYR-TYR-SER-ALA-LEU-NH2 neuropeptide Y,fragment 1-24 amide YPSKPDNPGEDAPAEDMARYYSAL-NH2

Description	Neuropeptide Y (1-24) (human) is a neuropeptide with potencies in inhibiting the electricity stimulated twitch response of rat vas deferens. Neuropeptide Y (1-24) (human) stimulates N-methyl-D-aspartate (NMDA)-induced neuronal activation in the rat CA3 region of the dorsal hippocampus in vivo[1][2].
Related Catalog	Signaling Pathways >> GPCR/G Protein >> Neuropeptide Y Receptor
In Vitro	Neuropeptide Y (1-24) (human) dose-dependently enhances N-methyl-D-aspartate (NMDA)-induced activation of CA3 dorsal hippocampus pyramidal neurons[1]. Neuropeptide Y (1-24) (human) selectively increases the amplitude of the twitch response to electrical stimulation at low micromolar concentrations but shows no affinity toward [3H]NPY brain receptor sites and no inhibition of the twitch response in the rat vas deferens preparation at concentrations up to 1.0 mM[2].

WGK Germany	3