1. 诱导疾病模型产品 GPCR/G Protein Neuronal Signaling
  2. 神经系统疾病模型 mAChR 5-HT Receptor
  3. 阿尔兹海默症模型
  4. Scopolamine hydrochloride

Scopolamine hydrochloride  (Synonyms: (-)-Scopolamine hydrochloride; Hyoscine hydrochloride)

目录号: HY-B2065
产品使用指南 技术支持

Scopolamine (Hyoscine) hydrochloride 是一种能透过血脑屏障的高亲和力毒蕈碱拮抗剂。Scopolamine hydrochloride 可竞争性拮抗 5-HT3 受体,IC50 为 2.09 μM。Scopolamine hydrochloride 能够诱导动物认知记忆缺陷。Scopolamine hydrochloride 可用于预防术后恶心呕吐、晕动病和神经系统等疾病的研究。

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Scopolamine hydrochloride

Scopolamine hydrochloride Chemical Structure

CAS No. : 55-16-3

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Scopolamine hydrochloride 的其他形式现货产品:

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Scopolamine (Hyoscine) hydrochloride is a high-affinity muscarinic antagonist that can cross the blood-brain barrier. Scopolamine hydrochloride competitively antagonizes 5-HT3 receptors with an IC50 of 2.09 μM. Scopolamine hydrochloride can induce cognitive and memory deficits in animals. Scopolamine hydrochloride can be used in the research of preventing postoperative nausea and vomiting, motion sickness, nervous system diseases, etc[1][2][3][4][5].

IC50 & Target[1]

5-HT3 Receptor

2.09 μM (IC50)

体外研究
(In Vitro)

Scopolamine hydrochloride 阻断烟碱乙酰胆碱受体 (IC50 = 928 μM),并增加 α7 nACh 受体的表达。Scopolamine hydrochloride 与 0.6 nM [3H]Granisetron 呈浓度依赖性竞争作用,平均 pKi 为 5.17 (Ki=6.76 μM)。Granisetron (HY-B0071) 荧光标记物 与 Scopolamine hydrochloride 进行浓度依赖性竞争,平均 pKi 为 5.31 (Ki = 4.90 μM)。Scopolamine hydrochloride 可阻断毒蕈碱受体并诱发认知障碍[1]
Scopolamine (0.1-3 mM;作用 24 小时) hydrochloride 可诱导 SH-SY5Y 细胞的细胞毒性、活性氧 (ROS) 生成和凋亡[6]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[6]

Cell Line: Human neuroblastoma SH-SY5Y cell line
Concentration: 0.1-3 mM (usually 2 mM)
Incubation Time: 24 hours
Result: Exposure to 1-3 mM for 24 hours significantly decreased human neuroblastoma SH-SY5Y cell viability in a dose-dependent manner. In all subsequent experiments, 2 mM resulted in 50.6% loss in cell viability.
体内研究
(In Vivo)

注意
请勿仅参考一篇文章来确定实验条件。建议在正式实验前,通过预实验确定最佳实验条件 (动物品系、年龄、剂量、频率及周期、检测时间及指标等)。

Scopolamine (1 mg/kg;腹腔注射;一次) 可在小鼠中导致与胆碱能神经传递减弱相关的记忆障碍,并增加与脑内氧化应激相关的过程[7]
Scopolamine 可用于诱导记忆障碍模型[4]

诱导记忆障碍模型
致病原理
Scopolamine 是一种选择性乙酰胆碱受体拮抗剂,通过占据突触后膜上的受体位点来降低突触处乙酰胆碱的有效性。
具体造模方法:
小鼠: Mus musculus Swiss • 2 月龄 • 25-30 g
给药方式:1 mg/kg/day,连续 7 天 • 腹腔注射
Note
造模成功指标
行为-T 迷宫测试: 增加进入首选臂的等待时间。减少了首选组的进入次数和停留时间,增加了其他组的进入次数和停留时间。
行为-旷场实验: 减少在旷场中心的时间,水平得分和垂直得分减少。
行为-物体识别: 增加发现并停留在熟悉物体上的时间。对新物体的探索次数减少。
分子水平变化: 谷胱甘肽水平降低。大脑中乙酰胆碱酯酶的活性增加。
相关产品Streptozotocin (HY-13753); Lipopolysaccharide (HY-D1056)

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Naive male Swiss mice weighing 20-25[7]
Dosage: 1 mg/kg
Administration: Administered intraperitoneally (i.p.); to measure the memory acquisition processes, Scopolamine was administered 20 min before the pretest; to measure the memory consolidation processes, Scopolamine was administered immediately after the pretest
Result: There was a significant decrease in the index of latency (IL) value as compared with the saline-treated mice, at the used dose impaired acquisition of memory and learning.
Clinical Trial
分子量

339.81

Formula

C17H22ClNO4

CAS 号
结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • 稀释计算器

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Scopolamine hydrochloride
目录号:
HY-B2065
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