[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 |
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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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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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CART (55-102) (human...
Cocaine- and amphetamine-regulated transcript (CART) with potent appetite-suppressing activity. Satiety factor; inhibits normal and starvation-induced feeding. Closely related to the actions of leptin and neuropeptide Y; blocks the neuropeptide Y-induced feeding response.
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SHA 68
SHA 68 is a potent and selective non-peptide antagonist of neuropeptide S receptor (NPSR)(NPSR Asn107 and NPSR Ile107 with IC50s of 22.0 and 23.8 nM, respectively).
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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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