1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. Spiradoline

Spiradoline (U-62066) 是一种芳基乙酰胺,是一种选择性 kappa 阿片受体 (κ-opioid receptor, KOR) 激动剂,在豚鼠中的 Ki 为 8.6 nM。Spiradoline 对 μ 和 δ 受体的 Ki 值分别为 252 nM 和 9400 nM。Spiradoline 具有强效的利尿,止痛,抗心律失常,镇咳,神经保护作用,并易于穿过血脑屏障。

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Spiradoline Chemical Structure

Spiradoline Chemical Structure

CAS No. : 87151-85-7

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Spiradoline 的其他形式现货产品:

Customer Review

Other Forms of Spiradoline:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Spiradoline (U-62066), an arylacetamide, is a selective kappa opioid receptor (KOR) agonist with a Ki of 8.6 nM in guinea pig. The Ki values of Spiradoline for μ and δ receptors are 252 nM and 9400 nM, respectively. Spiradoline has potent diuretic, analgesic, antiarrythmic, antitussive, neuroprotective properties and easily penetrates the blood-brain barrier[1][2].

IC50 & Target

Ki: 8.6 nM (κ-opioid receptor in guinea pig), 252 nM (μ-receptor) and 9400 nM (δ-receptor)[2]

体外研究
(In Vitro)

Using the patch-clamp method in isolated rat cardiac myocytes, indicated that Spiradoline (15 to 500 μM) produces its antiarrythmic effect via blockade of sodium channels (and at the higher doses also of potassium currents) in myocardial tissue. Thus, Spiradoline reduces the peak sodium current, increased the decay rate of the transient outward potassium current, and reduced the sustained plateau potassium amplitude[2].

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

体内研究
(In Vivo)

Spiradoline (U-62066; 0.1-0.4 mg/kg; subcutaneous injection; once; Sprague-Dawley rats) treatment dose-dependently reduces social behaviors in non-stressed adults, producing social avoidance at the highest dose tested, while younger animals displays reduced sensitivity to this socially suppressing effect of Spiradoline. In stressed animals, the socially suppressing effects of the Spiradoline are blunted at all ages, with juveniles and adolescents exhibiting increased social preference in response to certain doses of U-62066[1].

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

Animal Model: Juvenile, adolescent and adult Sprague-Dawley male and female rats exposured to repeated restraint[1]
Dosage: 0.1 mg/kg, 0.2 mg/kg, 0.3 mg/kg, and 0.4 mg/kg
Administration: Subcutaneous injection; once
Result: Dose-dependently reduced social behaviors in non-stressed adults, producing social avoidance at the highest dose tested.
Clinical Trial
分子量

425.39

同用名

U-62066

Formula

C22H30Cl2N2O2

CAS 号
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
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
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The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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:
Spiradoline
目录号:
HY-106756
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