β-Endorphin (human)
CAS No. 61214-51-5
β-Endorphin (human) ( ——— )
产品货号. M40159 CAS No. 61214-51-5
β-Endorphin, human 是存在于垂体和下丘脑中的重要的内源性肽,为阿片样 (opioid) 受体激动剂,尤其对 μ-opioid 受体和 δ-opioid 受体的亲和性更高;β-Endorphin, human 具有缓解疼痛的功效。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥4342 | 有现货 |
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| 10MG | ¥7192 | 有现货 |
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| 500MG | 获取报价 | 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β-Endorphin (human)
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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β-Endorphin, human 是存在于垂体和下丘脑中的重要的内源性肽,为阿片样 (opioid) 受体激动剂,尤其对 μ-opioid 受体和 δ-opioid 受体的亲和性更高;β-Endorphin, human 具有缓解疼痛的功效。
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产品描述β-Endorphin, human, a prominent endogenous peptide, existing in the hypophysis cerebri and hypothalamus, is an agonist of opioid receptor, with preferred affinity for μ-opioid receptor and δ-opioid receptor; β-Endorphin, human exhibits antinociception activity.
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体外实验———
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体内实验β-Endorphin, human is an agonist of opioid receptor, with preferred affinity for μ-opioid receptor and δ-opioid receptor. β-Endorphin exhibits anti-nociception activity by stimulating ε-opioid receptor, rather than μ-, δ-, and κ-opioid receptor. β-Endorphin has anti-nociception activity. Firstly, β-Endorphin combines together with the opioid receptors in hyperalgesia. Further, β-Endorphin suppresses the release of substance P at the level of spinal cord and blocks the conduction of pain on the primary sensory neurons. Moreover, β-Endorphin activates the endogenous analgesia system located in the CNS. In addition, β-Endorphin inhibits the conduction of pain and agitation of nociceptors to exert an analgesic effect.
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同义词———
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通路Endocrinology/Hormones
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靶点Opioid Receptor
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受体Opioid 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 Number61214-51-5
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分子量3464.98
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分子式C158H251N39O46S
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纯度>98% (HPLC)
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溶解度DMSO : 100 mg/mL (28.86 mM; ultraphonic; ) H2O : ≥ 50 mg/mL (14.43 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
1. Narita M, et al. Evidence for the existence of the beta-endorphin-sensitive "epsilon-opioid receptor" in the brain: the mechanisms of epsilon-mediated antinociception. Jpn J Pharmacol. 1998 Mar;76(3):233-53.?
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