NPY 5RA972
CAS No. 439861-56-0
NPY 5RA972 ( —— )
产品货号. M27671 CAS No. 439861-56-0
NPY 5RA972 是一种神经肽 Y Y5 受体拮抗剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥708 | 有现货 |
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| 10MG | ¥1131 | 有现货 |
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| 25MG | ¥2213 | 有现货 |
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| 50MG | ¥3283 | 有现货 |
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| 100MG | ¥4608 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称NPY 5RA972
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述NPY 5RA972 是一种神经肽 Y Y5 受体拮抗剂。
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产品描述NPY 5RA972 is a neuropeptide Y Y5 receptor antagonist.
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体外实验——
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体内实验——
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同义词——
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通路GPCR/G Protein
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靶点Neuropeptide Y Receptor
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受体PPARα
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研究领域——
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适应症——
化学信息
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CAS Number439861-56-0
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分子量351.45
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分子式C21H25N3O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 16.67 mg/mL (47.43 mM)
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SMILESCC(C)n1c2ccccc2c2c(C)c(NC(=O)N3CCOCC3)ccc12
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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Neuropeptide Y (22-3...
Neuropeptide Y (22-36), a 15 amino acid peptide, is a fragment of Neuropeptide Y.Neuropeptide Y (NPY) is a 36 amino-acid neuropeptide that is involved in various physiological and homeostatic processes in both the central and peripheral nervous systems. NPY has been identified as the most abundant peptide present in the mammalian central nervous system, which consists of the brain and spinal cord. It is secreted alongside other neurotransmitters such as GABA and glutamate.
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Spexin
Potent galanin receptor 2/3 (GAL2/GAL3) agonist (EC50 values are 45.7 and 112.2 nM, respectively). Exhibits no significant activity at galanin receptor 1. Endogenous satiety-inducing peptide; inhibits long chain fatty acid uptake by adipocytes and decreases food consumption in diet-induced obese mice and rats. Attenuates LH secretion in goldfish. Exhibits anxiolytic effects in vivo.
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[D-Trp34]-Neuropepti...
Potent neuropeptide Y (NPY) Y5 receptor agonist (pEC50 values are 7.82, 6.28, 6.44 and > 6 at rat Y5, Y4, Y1 and Y2 receptors respectively) that displays > 26-fold, > 1000-fold and > 1000-fold selectivity over Y1, Y2 and Y4 receptors respectively. Induces hyperphagia, body weight gain, adiposity, hypercholesterolemia, hyperinsulinemia and hyperleptinemia in vivo. Orally active.
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