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)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2356 | 有现货 |
|
| 10MG | ¥3781 | 有现货 |
|
| 25MG | ¥5924 | 有现货 |
|
| 50MG | ¥8119 | 有现货 |
|
| 100MG | ¥10530 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Spinorphin
-
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
-
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。
-
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.
-
体外实验——
-
体内实验——
-
同义词——
-
通路Endocrinology/Hormones
-
靶点Opioid Receptor
-
受体enkephalin degrading enzymes
-
研究领域——
-
适应症——
化学信息
-
CAS Number137201-62-8
-
分子量877
-
分子式C45H64N8O10
-
纯度>98% (HPLC)
-
溶解度——
-
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
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
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
关联产品
-
Endomorphin 1 acetat...
Endomorphin 1 acetate,一种高度选择性的,高亲和力的 μ-opioid 受体激动剂 (Ki: 1.11 nM),对 kappa3结合位点具有高亲和力,Ki 值为 20 到 30 nM 之间。Endomorphin 1 acetate 具有镇痛特性。
-
Salvinorin A
Salvinorin A 是一种非氮 κ-阿片类选择性激动剂。
-
Adrenorphin(3TFA)
Adrenorphin(3TFA) 是 μ-阿片受体 (Ki :12 nM) 的激动剂。
021-51111890
购物车()
sales@molnova.cn

