1. GPCR/G Protein Neuronal Signaling
  2. Cannabinoid Receptor
  3. O1918

O1918 是 non-CB1 受体和 GPR18 的选择性拮抗剂。

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O1918 Chemical Structure

O1918 Chemical Structure

CAS No. : 536697-79-7

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1mg (34.91 mM * 100 μL in Methyl acetate) ¥1100
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5mg (34.91 mM * 500 μL in Methyl acetate) ¥3800
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10mg (34.91 mM * 1 mL in Methyl acetate) ¥6000
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Customer Review

MCE 顾客使用本产品发表的 1 篇科研文献

查看 Cannabinoid Receptor 亚型特异性产品:

  • 生物活性

  • 实验参考方法

  • 纯度 & 产品资料

  • 参考文献

生物活性

O1918 is a selective non-CB1 receptor and GPR18 antagonist.

IC50 & Target

non-CB1 vascular cannabinoid receptor[1], GPR18[2].

体内研究
(In Vivo)

Decreases in HR, blood pressure, MBF and RBF by about 20 beats/min, 5-10 mmHg and 0.7 and 0.2 mL/min, respectively, are observed after injection of O1918 (3 µmol/kg). O1918 causes an inhibition of the anandamide-stimulated decreases in MBP, SBP and DBP by 55, 38 and 42% respectively. Similarly, this antagonist reduces the methanandamide-stimulated fall in SBP and DBP by 44 and 32%, respectively, and tends to diminish the decrease in MBP by 28%. O1918 also diminishes the fall in MBF and RBF induced by anandamide by 61 and 67% and that induced by methanandamide by 74 and 49% respectively. Cannabidiol does not affect basal cardiovascular parameters whereas O1918 decreases HR by about 15 beats/min and SBP, DBP and MBP by about 15 mmHg. In pithed rats anandamide (3 µmol/kg) causes only an increase in MBF and RBF. The anandamide-induced long-lasting fall in MBP, SBP and DBP is reduced by cannabidiol by 40-46% and by O-1918 by 55, 64 and 35, respectively[1].

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

分子量

286.41

Formula

C19H26O2

CAS 号
性状

液体

颜色

Colorless to light yellow

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Solution, -20°C, 2 years

纯度 & 产品资料

纯度: ≥96.0%

参考文献
Animal Administration
[1]

Rats[1]
In order to examine the influence of different receptor antagonists on the changes in cardiovascular parameters induced by anandamide or methanandamide (both in anaesthetized and pithed rats), the particular agonist is injected twice (S1 and S2, 20 min apart). Methanandamide is administered at 0.5 µmol/kg. S1 is applied 5 min after injection of saline solution or ruthenium red 3 (µmol/kg in pithed rats anaesthetized with urethane). Cannabidiol or O1918 (3 µmol/kg) or their solvents are administered 10 min before S2. AM 251, cannabidiol or O1918 (3 µmol/kg, each) are administered simultaneously with pancuronium[1].

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

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 *
= × ×

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:
O1918
目录号:
HY-103335
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