[Leu31,Pro34]-Neuropeptide Y (porcine)
CAS No. 125580-28-1
[Leu31,Pro34]-Neuropeptide Y (porcine) ( —— )
产品货号. M29590 CAS No. 125580-28-1
[Leu31,Pro34]-Neuropeptide Y是神经肽 Y (NPY) Y1 受体的选择性高亲和力激动剂,具有抗焦虑作用。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1701 | 有现货 |
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| 10MG | ¥2499 | 有现货 |
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| 25MG | ¥3850 | 有现货 |
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| 50MG | ¥5282 | 有现货 |
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| 100MG | ¥6912 | 有现货 |
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| 500MG | ¥13770 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称[Leu31,Pro34]-Neuropeptide Y (porcine)
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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[Leu31,Pro34]-Neuropeptide Y是神经肽 Y (NPY) Y1 受体的选择性高亲和力激动剂,具有抗焦虑作用。
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产品描述[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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体外实验——
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体内实验[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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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Neuropeptide Y Receptor
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研究领域——
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适应症——
化学信息
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CAS Number125580-28-1
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分子量4223
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分子式C190H286N54O56
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O : ≥ 100 mg/mL (23.68 mM)*)
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SMILES——
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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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SHA 68
SHA 68 是神经肽 S 受体 (NPSR) 的有效选择性非肽拮抗剂(NPSR Asn107 和 NPSR Ile107,IC50 分别为 22.0 和 23.8 nM)。
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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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[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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