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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M 1145
Potent and selective galanin receptor 2 (GAL2) agonist (EC50 = 38 nM, Ki values are 6.55, 497 and 587 nM at GAL2, GAL3 and GAL1 respectively). Has an additive effect on the signal transduction of galanin.
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Galanin (1-30), huma...
Galanin (1-30), human is a 30-amino acid neuropeptide, and acts as an agonist of GalR1 and GalR2 receptors, with Kis of both 1 nM. Endogenous peptide with multiple endocrine, metabolic and behavioral effects. Has been shown to have an action on intestinal smooth muscle, insulin and somatostatin release, and synaptic neurotransmission.
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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).
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