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TBHQ
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
TBHQ图片
CAS NO:1948-33-0
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
500mg电议
1 g电议
5 g电议
10 g电议

产品名称
特丁基对苯二酚
tert-Butylhydroquinone
产品介绍
TBHQ (tert-Butylhydroquinone) 是一种广泛使用的Nrf2激活剂,通过激活Nrf2来免受 Doxorubicin (DOX)-诱导的心脏毒性。TBHQ (tert-Butylhydroquinone) 也是一种ERK激活剂,逆转 Dehydrocorydaline (DHC) 对黑素瘤细胞增殖的抑制作用。
生物活性

TBHQ (tert-Butylhydroquinone) is a widely usedNrf2activator, protects against Doxorubicin (DOX)-induced cardiotoxicity through activation ofNrf2[1]. TBHQ (tert-Butylhydroquinone) is also anERKactivator; rescues Dehydrocorydaline (DHC)-induced cell proliferation inhibitionin melanoma[2].

IC50& Target[1][2]

ERK

 

Nrf2

 

Autophagy

 

体外研究
(In Vitro)

TBHQ (t-butylhydroquinone; tBHQ; 0-100 μM; 48 hours; H9c2 cells) alone does not affect H9c2 cells viability. Pre-incubation of the H9c2 cells with various concentrations of tBHQ for 24 hours enhances cell viability which is decreased due to exposure to ethanol in a dose-dependent manner. Treatment with tBHQ markedly enhances the viability of H9c2 cardiomyocytes exposed to ethanol[3].
TBHQ (5 μM; 15 min; H9c2 cells) treatment significantly reduces the amount of apoptotic cells exposed to ethanol[3].
TBHQ (5 μM; H9c2 cells) pre-treatment markedly inhibites the ethanol-induced increase in caspase-3 and Bax expression, and enhances Bcl-2 expression[3].

Cell Viability Assay[3]

Cell Line:H9c2 cells
Concentration:0 μM, 0.625 μM, 1.25 μM, 2.5 μM, 5 μM, 10 μM, 20 μM, 50 μM and 100 μM
Incubation Time:48 hours
Result:Enhanced the viability of H9c2 cardiomyocytes exposed to ethanol.

Apoptosis Analysis[3]

Cell Line:H9c2 cells
Concentration:5 μM
Incubation Time:
Result:Lowered the amount of apoptotic cells exposed to ethanol.

Western Blot Analysis[3]

Cell Line:H9c2 cells
Concentration:5 μM
Incubation Time:
Result:Inhibited the ethanol-induced increase in caspase-3 and Bax expression, and enhanced Bcl-2 expression.
体内研究
(In Vivo)

TBHQ treatment (50 mg/kg; Intraperitoneal injection; three injections at intervals of 8 h that began 1-h post ICH; CD-1 mice) augments the DNA-Binding activity of Nrf2, attenuates oxidative brain damage and acute neurological deficits afterintracerebral hemorrhage (ICH), attenuates microglial activation with concomitant reduction in the release of proinflammatory cytokine interleukin-1β (IL-1β). TBHQ has the efficacy of post-injury administration in attenuating acute neurological injury after ICH[4].

Animal Model:Male CD-1 mice (8-10 weeks old)[4]
Dosage:50 mg/kg
Administration:Intraperitoneal injection; three injections at intervals of 8 hours that began 1h post ICH.
Result:The treatment augmented the DNA-binding activity of Nrf2, attenuated brain oxidative damage, attenuated the microglial activation and the expression of IL-1β.
分子量

166.22

性状

Solid

Formula

C10H14O2

CAS 号

1948-33-0

中文名称

特丁基对苯二酚;叔丁基对苯二酚

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : ≥ 56.66 mg/mL(340.87 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM6.0161 mL30.0806 mL60.1612 mL
5 mM1.2032 mL6.0161 mL12.0322 mL
10 mM0.6016 mL3.0081 mL6.0161 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℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 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: 50%PEG300   50% saline

    Solubility: 20 mg/mL (120.32 mM); Clear solution; Need ultrasonic

  • 2.

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

    Solubility: ≥ 2.5 mg/mL (15.04 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (15.04 mM,饱和度未知) 的澄清溶液。

    以 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;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
  • 3.

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

    Solubility: ≥ 2.5 mg/mL (15.04 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (15.04 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL20% 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
  • 4.

    请依序添加每种溶剂: 10% DMSO    90%corn oil

    Solubility: ≥ 2.5 mg/mL (15.04 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (15.04 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 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玉米油中,混合均匀。

*以上所有助溶剂都可在本网站选购。