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[Leu31,Pro34]-Neuropeptide Y (porcine)
CAS No. 125580-28-1
[Leu31,Pro34]-Neuropeptide Y (porcine)( —— )
Catalog No. M29590 CAS No. 125580-28-1
[Leu31,Pro34]-Neuropeptide Y (porcine), is a selective and high affinity agonist of neuropeptide Y (NPY) Y1 receptor with anxiolytic effects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 183 | In Stock |
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| 10MG | 282 | In Stock |
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| 25MG | 466 | In Stock |
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| 50MG | 608 | In Stock |
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| 100MG | 831 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 1665 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name[Leu31,Pro34]-Neuropeptide Y (porcine)
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NoteResearch use only, not for human use.
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Brief Description[Leu31,Pro34]-Neuropeptide Y (porcine), is a selective and high affinity agonist of neuropeptide Y (NPY) Y1 receptor with anxiolytic effects.
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Description[Leu31,Pro34]-Neuropeptide Y (porcine), is a selective and high affinity agonist of neuropeptide Y (NPY) Y1 receptor with anxiolytic effects.(In Vitro):In a series of human neuroblastoma cell lines and on rat PC-12 cells, [Leu31,Pro34]-Neuropeptide Y (porcine) displaced radiolabeled NPY from cells expressing Y1 receptors.
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In Vitro——
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In Vivo[Leu31,Pro34]-Neuropeptide Y (porcine) displaces radiolabeled NPY from cells that express Y1 receptors in a series of human neuroblastoma cell lines and on rat PC-12 cells.
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Synonyms——
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PathwayGPCR/G Protein
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TargetNeuropeptide Y Receptor
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RecptorNeuropeptide Y Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number125580-28-1
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Formula Weight4223
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Molecular FormulaC190H286N54O56
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : ≥ 100 mg/mL (23.68 mM)*)
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SMILES——
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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[Leu31,Pro34]-Neurop...
High affinity neuropeptide Y Y1 receptor agonist (Ki = 0.39 nM). Also shows affinity for Y4 and Y5 receptors.
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M617
Selective galanin GAL1 receptor agonist (Ki values are 0.23 and 5.71 nM for GAL1 and GAL2 receptors respectively). Enhances food consumption in rats following i.c.v. administration and reduces CAP-induced inflammatory pain.
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GR 231118
Potent neuropeptide Y (NPY) Y1 receptor antagonist (pA2 = 10 and 10.5 at rY1 and hY1, receptors respectively). Also a potent and selective NPY Y4 receptor agonist (pEC50 values are 6.0, 8.6 and 6.1 for rY2, hY4 and rY5 receptors respectively). Suppresses food intake in rats in vivo. Also has affinity for neuropeptide FF (NPFF) receptors in vitro (Ki = 43-73 nM).
