1. NF-κB GPCR/G Protein Neuronal Signaling Autophagy Apoptosis
  2. NF-κB Opioid Receptor Autophagy Apoptosis
  3. Sinomenine

Sinomenine  (Synonyms: 青藤碱)

目录号: HY-15122 纯度: 99.94%
Data Sheet SDS COA 产品使用指南 技术支持

Sinomenine 是来自 Sinomenium acutum 的一种生物碱,是 NF-κB 活化的阻断剂。Sinomenine 也是 μ 阿片受体 (μ-opioid receptor) 激活剂。

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Sinomenine Chemical Structure

Sinomenine Chemical Structure

CAS No. : 115-53-7

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规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥605
In-stock
100 mg ¥550
In-stock
200 mg   询价  
500 mg   询价  

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Customer Review

Other Forms of Sinomenine:

    Sinomenine purchased from MCE. Usage Cited in: Free Radic Biol Med. 2018 Jun 2;124:205-213.  [Abstract]

    Total and phosphorylation levels of p65 in MCF7 and MDAMB231 after Sinomenine hydrochloride (SH) treatment at 24 h.
    • 生物活性

    • 实验参考方法

    • 纯度 & 产品资料

    • 参考文献

    生物活性

    Sinomenine, an alkaloid extracted from Sinomenium acutum, is a blocker of the NF-κB activation[1]. Sinomenine also is an activator of μ-opioid receptor[2].

    IC50 & Target

    μ Opioid Receptor/MOR

     

    细胞效力
    (Cellular Effect)
    Cell Line Type Value Description References
    KB IC50
    > 759 μM
    Compound: Sinomenine
    Cytotoxicity against human KB cells after 72 hrs
    Cytotoxicity against human KB cells after 72 hrs
    [PMID: 11141105]
    NIH3T3 IC50
    > 100 μM
    Compound: 1
    Cytotoxicity against mouse NIH/3T3 cells assessed as growth inhibition after 24 hrs by MTT assay
    Cytotoxicity against mouse NIH/3T3 cells assessed as growth inhibition after 24 hrs by MTT assay
    [PMID: 23357309]
    RAW264.7 IC50
    > 100 μM
    Compound: 1
    Cytotoxicity against mouse RAW264.7 cells after 24 hrs by MTT assay
    Cytotoxicity against mouse RAW264.7 cells after 24 hrs by MTT assay
    [PMID: 21530276]
    RAW264.7 IC50
    > 200 μM
    Compound: 1
    Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess method
    Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess method
    [PMID: 22325804]
    RAW264.7 IC50
    > 200 μM
    Compound: 1
    Cytotoxicity against mouse RAW264.7 cells after 24 hrs by MTT assay
    Cytotoxicity against mouse RAW264.7 cells after 24 hrs by MTT assay
    [PMID: 22325804]
    体外研究
    (In Vitro)

    Cell viability gradually decreased with increasing Sinomenine concentration. The migration ability of MDA-MB-231 cells is significantly weakened by 0.25, 0.5, and 1 mM of Sinomenine treatment. The wound-healing assay reveals that 0.25 and 0.5 mM Sinomenine significantly suppress the healing of the wound. When the MDA-MB-231 cells are treated with 0.5 mM Sinomenine, the healing progress is about 50%, but in the group treated with 0.25 mM Sinomenine and the untreated control, the healing is about 80% and nearly 95%, respectively. The IB assay following inhibitor of NF-κB (IκB) antibody IP shows that the binding of NF-κB to IκB is inhibited by Sinomenine treatment in a dose-dependent manne[1].

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

    体内研究
    (In Vivo)

    Sinomenine (i.p.) produces antinociception in the hot plate and tail flick tests in male rats at 40 mg/kg, but not at lower doses (10 or 20 mg/kg). At 10 to 40 mg/kg Sinomenine does not produce any observable side effect such as sedation, allergy or motor impairments. Antinociception is also seen mice at 60 min following 80 mg/kg i.p. Sinomenine, but not at lower doses (20 or 40 mg/kg), in the tail flick test. Sinomenine at 80 mg/kg i.p. does not produce any observable side effects in mice. I.p or p.o. Sinomenine at 40 or 80 mg/kg dose-dependently reduces mechanical hypersensitivity in nerve injured mice. I.p. Sinomenine at 40 mg/kg, but not lower doses or vehicle, significantly decreases mechanical and cold allodynia for up to 240 min without producing motor deficits or sedation[3]. At doses of 10 to 40 mg/kg, Sinomenine dose-dependently increases the paw withdrawal threshold. In non-chronic constriction injury (CCI) healthy rats, Sinomenine at the dose range of 10 to 40 mg/kg does not change the immobility behavior in the forced swimming test[4].

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

    Clinical Trial
    NCT NumberSponsorConditionStart DatePhase
    NCT05764304Shanghai 6th People´s Hospital
    Knee Osteoarthritis
    February 28, 2023Phase 3
    分子量

    329.39

    Formula

    C19H23NO4

    CAS 号
    性状

    固体

    颜色

    White to off-white

    中文名称

    青藤碱

    结构分类
    初始来源
    运输条件

    Room temperature in continental US; may vary elsewhere.

    储存方式

    4°C, protect from light

    *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

    溶解性数据
    细胞实验: 

    DMSO 中的溶解度 : 50 mg/mL (151.80 mM; 超声助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

    1M HCl 中的溶解度 : 25 mg/mL (75.90 mM; 超声助溶; 酸性条件溶解 (HCL 调节,pH≈1))

    配制储备液
    浓度 溶剂体积 质量 1 mg 5 mg 10 mg
    1 mM 3.0359 mL 15.1796 mL 30.3591 mL
    5 mM 0.6072 mL 3.0359 mL 6.0718 mL
    查看完整储备液配制表

    * 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
    储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

    • 摩尔计算器

    • 稀释计算器

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

    质量
    =
    浓度
    ×
    体积
    ×
    分子量 *

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

    This equation is commonly abbreviated as: C1V1 = C2V2

    浓度 (start)

    C1

    ×
    体积 (start)

    V1

    =
    浓度 (final)

    C2

    ×
    体积 (final)

    V2

    动物实验:

    请根据您的 实验动物和给药方式 选择适当的溶解方案。

    以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
    ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用
    以下溶剂前显示的百分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

    • 方案 一

      请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.5 mg/mL (7.59 mM); 澄清溶液

      此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。

      1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL

      生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。
    • 方案 二

      请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.5 mg/mL (7.59 mM); 澄清溶液

      此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。

      1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液 中,混合均匀。

      2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。

    扫码获得
    动物溶解方案

    动物溶解方案计算器
    请输入动物实验的基本信息:

    给药剂量

    mg/kg

    动物的平均体重

    g

    每只动物的给药体积

    μL

    动物数量

    由于实验过程有损耗,建议您多配一只动物的量
    请输入您的动物体内配方组成:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    如果您的动物是免疫缺陷鼠或者体弱鼠,建议 DMSO 中的在最后工作液体系中的占比尽量不超过 2%。
    方案所需 助溶剂 包括:DMSO PEG300/PEG400Tween 80,均可在 MCE 网站选购。
    纯度 & 产品资料

    纯度: 99.94%

    参考文献
    Cell Assay
    [1]

    The MDA-MB-231 human triple negative and 4T1 mouse breast cancer cell lines are used in this study. For the experiments, the cells are grown in 24-well plates at 3.5×104/well. Following incubation for 24 or 48 h in medium containing different concentrations of Sinomenine, proliferation of the cells are detected with Cell Counting Kit-8 solution according to the manufacturer's instructions[1].

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

    Animal Administration
    [4]

    Male Sprague-Dawley rats weighing of 250 to 300 g are used in this experiment. For the duration of action of acute Sinomenine study, different doses of Sinomenine (10 to 40 mg/kg) are administered 1 day after surgery and then paw withdrawal threshold is measured every 30 min for 4 hours. For the study involving daily Sinomenine treatment, mechanical hyperalgesia measure is performed 3 h after daily drug treatment. For antagonist studies, antagonists were given 10 min prior to 40 mg/kg Sinomenine administration[3].

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

    参考文献

    完整储备液配制表

    * 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
    储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

    可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
    1M HCl / DMSO 1 mM 3.0359 mL 15.1796 mL 30.3591 mL 75.8979 mL
    5 mM 0.6072 mL 3.0359 mL 6.0718 mL 15.1796 mL
    10 mM 0.3036 mL 1.5180 mL 3.0359 mL 7.5898 mL
    15 mM 0.2024 mL 1.0120 mL 2.0239 mL 5.0599 mL
    20 mM 0.1518 mL 0.7590 mL 1.5180 mL 3.7949 mL
    25 mM 0.1214 mL 0.6072 mL 1.2144 mL 3.0359 mL
    30 mM 0.1012 mL 0.5060 mL 1.0120 mL 2.5299 mL
    40 mM 0.0759 mL 0.3795 mL 0.7590 mL 1.8974 mL
    50 mM 0.0607 mL 0.3036 mL 0.6072 mL 1.5180 mL
    60 mM 0.0506 mL 0.2530 mL 0.5060 mL 1.2650 mL
    DMSO 80 mM 0.0379 mL 0.1897 mL 0.3795 mL 0.9487 mL
    100 mM 0.0304 mL 0.1518 mL 0.3036 mL 0.7590 mL

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    产品名称:
    Sinomenine
    目录号:
    HY-15122
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