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Velneperit
CAS No. 342577-38-2
Velneperit( S2367 )
Catalog No. M22270 CAS No. 342577-38-2
Velneperit is potent and selective neuropeptide Y (NPY) Y5 receptor under evaluating for treatment of obesity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 75 | In Stock |
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| 2MG | 42 | In Stock |
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| 5MG | 68 | In Stock |
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| 10MG | 116 | In Stock |
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| 25MG | 258 | In Stock |
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| 50MG | 431 | In Stock |
|
| 100MG | 634 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameVelneperit
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NoteResearch use only, not for human use.
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Brief DescriptionVelneperit is potent and selective neuropeptide Y (NPY) Y5 receptor under evaluating for treatment of obesity.
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DescriptionVelneperit is potent and selective neuropeptide Y (NPY) Y5 receptor under evaluating for treatment of obesity.
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In Vitro——
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In Vivo——
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SynonymsS2367
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PathwayGPCR/G Protein
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TargetNeuropeptide Y Receptor
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Recptorneuropeptide Y (NPY) Y5 receptor
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Research AreaOthers
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IndicationObesity
Chemical Information
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CAS Number342577-38-2
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Formula Weight407.45
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Molecular FormulaC17H24F3N3O3S
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Purity>98% (HPLC)
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SolubilityDMSO:29 mg/mL (71.17 mM)
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SMILESFC(F)(F)C1=CN=C(NC([C@H]2CC[C@H](NS(=O)(C(C)(C)C)=O)CC2)=O)C=C1
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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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M871
Selective galanin GAL2 receptor antagonist (Ki values are 13.1 and 420 nM for GAL2 and GAL1 receptors respectively). Blocks the pro-nociceptive effect of GAL2 receptor agonists.
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Neuropeptide S (Mous...
Potent endogenous neuropeptide S receptor (NPSR) agonist (EC50 = 3 nM). Induces mobilization of intracellular Ca2+. Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.
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Neuropeptide SF (mou...
Neuropeptide FF receptor agonist (Ki values are 48.4 and 12.1 nM for NPFF1 and NPFF2, respectively). Potentiates the antinociceptive action of morphine in vivo and reverses the loss of morphine potency in tolerant animals. Also increases the amplitude of the sustained current of heterologously expressed acid sensing ion channel 3 (ASIC3) (EC50 ~ 50 μM).
