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SNC 80 (NIH 10815) 是有效的,高度选择性的非肽类 δ 阿片 (δ-opioid) 受体激动剂,Ki 为1.78 nM,IC50 为 2.73 nM。SNC80 还以 EC50 为 52.8 nM 来选择性激活 HEK293 细胞中的 μ-δ 异聚体。SNC80 具有抗伤害性,抗痛觉过敏和抗抑郁样作用,并可用于多种头痛症的研究。
SNC 80 (NIH 10815) 是有效的,高度选择性的非肽类 δ 阿片 (δ-opioid) 受体激动剂,Ki 为1.78 nM,IC50 为 2.73 nM。SNC80 还以 EC50 为 52.8 nM 来选择性激活 HEK293 细胞中的 μ-δ 异聚体。SNC80 具有抗伤害性,抗痛觉过敏和抗抑郁样作用,并可用于多种头痛症的研究。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 373 | 现货 | |
5 mg | ¥ 881 | 现货 | |
10 mg | ¥ 1,530 | 现货 | |
25 mg | ¥ 3,680 | 现货 | |
50 mg | ¥ 4,930 | 现货 | |
100 mg | ¥ 6,870 | 现货 |
产品描述 | SNC 80 (NIH 10815) is a potent, highly selective and non-peptide δ-opioid receptor agonist, Ki = 1.78 nM, IC50 = 2.73 nM. SNC80 also selectively activates μ-δ heteromer in HEK293 cells with an EC50 of 52.8 nM. SNC80 shows antinociceptive, antihyperalgesic and antidepressant‐like effects. SNC80 has the potential for multiple headache disorders treatment. |
体外活性 | SNC80 selectively activates μ-δ heteromer in HEK293 cells, EC50 = 52.8 nM. SNC80 exhibits substantially greater activity in cells coexpressing μ- and δ-opioid receptors than in cells either singly expressing δ-opioid receptors or coexpressing δ- and κ-opioid receptors [4]. |
体内活性 | SNC80 (10 mg/kg; intraperitoneal injection; once) treatment significantly attenuated this allodynia caused by overuse of Sumatriptan in C57BL6/J mice [1]. |
别名 | Snc-80, SNC80, NIH 10815 |
分子量 | 449.63 |
分子式 | C28H39N3O2 |
CAS No. | 156727-74-1 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||
溶解度信息 | DMSO: 1 mg/mL (2.22 mM), Sonication is recommended. | ||||||||||
溶液配制表 | |||||||||||
DMSO
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