
Spinorphin
CAS No. 137201-62-8
Spinorphin ( —— )
产品货号. M22044 CAS No. 137201-62-8
Spinorphin 是一种七肽,是一种有效的脑啡肽降解酶抑制剂。Spinorphin 抑制中型和小型培养的大鼠 DRG 神经元中由去极化和辣椒素选择性诱发的细胞质 Ca(2+) ([Ca(2+)]i) 瞬变。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥2082 | 有现货 |
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10MG | ¥3216 | 有现货 |
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25MG | ¥5370 | 有现货 |
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50MG | ¥7655 | 有现货 |
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100MG | ¥10368 | 有现货 |
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200MG | 获取报价 | 有现货 |
![]() ![]() |
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Spinorphin
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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Spinorphin 是一种七肽,是一种有效的脑啡肽降解酶抑制剂。Spinorphin 抑制中型和小型培养的大鼠 DRG 神经元中由去极化和辣椒素选择性诱发的细胞质 Ca(2+) ([Ca(2+)]i) 瞬变。
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产品描述Spinorphin is a heptapeptide, and is a potent enkephalin-degrading enzymes inhibitor.Spinorphin inhibited cytoplasmic Ca(2+) ([Ca(2+)]i) transients, evoked by depolarization and capsaicin selectively in medium and small cultured rat DRG neurons.?Spinorphin (10-300 M) inhibited the Ca(2+) signals in concentration dependant manner in small- and medium diameter DRG neurons.?Capsaicin produced [Ca(2+)]i responses only in small- and medium-sized DRG neurons, and pre-treatment with spinorphin significantly attenuated these [Ca(2+)]i responses.?Spinorphin significantly inhibited the functions of polymorphonuclear neutrophils (PMNs) by suppressing the binding of fMLF to its receptor on PMNs. Further, this inhibitor suppressed the carrageenan-induced accumulation of PMN in mouse air pouches after intravenous administration. These results indicate that spinorphin may be an endogenous anti-inflammatory regulator. The possible role of spinorphin and its analog as regulators in pain and inflammation will be discussed.
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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Endocrinology/Hormones
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靶点Opioid Receptor
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受体enkephalin degrading enzymes
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研究领域——
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适应症——
化学信息
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CAS Number137201-62-8
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分子量877
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分子式C45H64N8O10
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纯度>98% (HPLC)
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溶解度——
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SMILESCC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC1=CNC2=CC=CC=C12)C(=O)N[C@@H]([C@@H](C)O)C(O)=O
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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. Ayar A , Ozcan M , Kemal Tu?rul Kuzgun, et al. Spinorphin inhibits membrane depolarization- and capsaicin-induced intracellular calcium signals in rat primary nociceptive dorsal root ganglion neurons in culture[J]. Journal of Receptor Research, 2015, 35(6):550-558.2. YAMAMOTO,Y. Spinorphin as an endogenous inhibitor of enkephalin-degrading enzymes: roles in pain and inflammation.[J]. Current Protn & Peptide ence, 2002, 3(6):-.
产品手册




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