Coenzyme Q0  (货号:B26736)

说明书
Coenzyme Q0
规格价格
Free Sample (0.1 - 0.2 mg) 询价
1 g 询价
5 g 询价
500 mg ¥350.00 加购物车
10 mM * 1 mL in DMSO ¥385.00 加购物车

货号:B26736

生物活性 Coenzyme Q0 (CoQ0) is a potent, oral active ubiquinone compound can be derived from Antrodia cinnamomea. Coenzyme Q0 induces apoptosis and autophagy, suppresses of HER-2/AKT/mTOR signaling to potentiate the apoptosis and autophagy mechanisms. Coenzyme Q0 regulates NFκB/AP-1 activation and enhances Nrf2 stabilization in attenuation of inflammation and redox imbalance. Coenzyme Q0 has anti-angiogenic activity through downregulation of MMP-9/NF-κB and upregulation of HO-1 signaling.
CAS 605-94-7
中文名称
分子量 182.18
体外研究

Coenzyme Q0 (0-40 µM; 24 h) and inhibits viability and growth of human ovarian carcinoma cells.
Coenzyme Q0 (CoQ0) (0-30 µM; 24 h; SKOV-3 cells) has anti-proliferative activity through induction of G2/M cell-cycle arrest and reduction of cell-cycle regulatory proteins.
Coenzyme Q0 (CoQ0) (0-30 µM; 0-30 min; SKOV-3 cells) increases intracellular ROS levels to promote SKOV-3 cell death.
Coenzyme Q0 (CoQ0) (0-30 µM; 24 h; SKOV-3 cells) induces autophagy by increase accumulation of LC3-II, GFP-LC3 puncta, AVOs formation and Beclin-1/Bcl-2 dysregulation.
Coenzyme Q0 (CoQ0) (0-30 µM; 24 h; SKOV-3 cells) induces apoptosis by mitochondrial (caspase-3, PARP and Bax/Bcl-2 dysregulation) and ER stress (caspase-12 and Hsp70) signals.
Coenzyme Q0 (CoQ0) (30 µM; 24 h; SKOV-3 cells) suppresses of HER-2/AKT/mTOR signaling to potentiate the apoptosis and autophagy mechanisms.
Coenzyme Q0 (CoQ0) (0-10 µM; 0.5-18 h; RAW264.7 cells) regulates NFκB/AP-1 activation and enhances Nrf2 stabilization.
Coenzyme Q0 (CoQ0) (5 µM; 0-12 h; EA.hy 926 cells) has anti-angiogenic activity in EA.hy 926 cells.

The accuracy of these methods have not been independently confirmed. They are for reference only.

Cell Viability Assay

Cell Line:SKOV-3, A2780 and A2870/CP70 cells
Concentration:0, 10, 20, 30 and 40 µM
Incubation Time:24 hours
Result:Decreased viability with the IC50 values of 26.6 µM, 27.3 µM and 28.4 µM for SKOV-3, A2780 and A2870/CP70 cells, respectively.

Cell Cycle Analysis

Cell Line:SKOV-3, A2780 and A2870/CP70 cells
Concentration:0, 10, 20 and 30 µM
Incubation Time:24 hours
Result:Arrested cell cycle at G2/M phase and reduced cell-cycle proteins in SKOV-3 cells.

Apoptosis Analysis

Cell Line:SKOV-3, A2780 and A2870/CP70 cells
Concentration:0, 5, 15 and 30 µM
Incubation Time:24 hours
Result:Promoted the conversion of LC3–1 to LC3-II and increased the LC3-II accumulation. Increased Bax/Bcl-2 ratio in a dose-dependent manner.

Apoptosis Analysis

Cell Line:SKOV-3 cells
Concentration:0, 10, 20 and 30 µM
Incubation Time:24 hours
Result:Had the percentage of early apoptotic cells are 25.1%, 34% and 36% for 10, 20 and 30 µM, respectively.

Western Blot Analysis

Cell Line:SKOV-3 cells
Concentration:0, 5, 15 and 30 µM
Incubation Time:24 hours
Result:Activated of caspase-3 and cleavaged of PARP. Increased the expressions of caspase-12, HSP-70 and Bax in a dose-dependent manner, decreased the expressions of Bcl-2.

Western Blot Analysis

Cell Line:SKOV-3 cells
Concentration:30 µM
Incubation Time:24 hours
Result:Decreased the phosphorylated HER-2 (Y1221) levels, p-AKT (Ser473) and p-mTOR (S2448) levels.

Western Blot Analysis

Cell Line:RAW264.7 cells
Concentration:0, 2.5, 5 and 10 µM
Incubation Time:0.5-18 hours
Result:Inhibited iNOS/COX-2 protein expressions with reductions of NO, PGE2, TNF-α and IL-1β secretions.

Western Blot Analysis

Cell Line:EA.hy 926 cells
Concentration:5 µM
Incubation Time:0, 1, 3, 6 and 12 hours
Result:Increased expressions of heme oxygenase-1 (HO-1) and γ-glutamylcysteine synthetase (γ-GCLC), inhibits protein expressions of matrix metalloproteinase-9 (MMP-9), reduces TNF-α-induced nuclear translocation and transcriptional activation of nuclear factor-κB (NF-κB).
体内研究
形式 Solid
运输条件 Room temperature in continental US; may vary elsewhere.
保存条件
溶解性
In Vitro: 

DMSO : 50 mg/mL (274.45 mM; Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM5.4891 mL27.4454 mL54.8908 mL
5 mM1.0978 mL5.4891 mL10.9782 mL
10 mM0.5489 mL2.7445 mL5.4891 mL
*

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。-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。

In Vivo:

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

  • 1.

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

    Solubility: ≥ 1.67 mg/mL (9.17 mM); Clear solution

    此方案可获得 ≥ 1.67 mg/mL (9.17 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 16.7 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液
  • 2.

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

    Solubility: ≥ 1.67 mg/mL (9.17 mM); Clear solution

    此方案可获得 ≥ 1.67 mg/mL (9.17 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 16.7 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。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
*以上所有助溶剂都可在 MCE 网站选购。

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