货号:A348334
同义名:
2,5-二特丁基对苯二酚
/ BHQ
2,5-Di-tert-butylhydroquinone是一种选择性的肌浆网钙ATP酶(SERCA)抑制剂,具有调节5-LO和COX-2活性的能力,IC50分别为1.8和14.1 μM。
HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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| 产品名称 | ATPase ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| (-)-Blebbistatin | 99%+ | ||||||||||||||||||
| PF 03716556 |
++++
H+/K+-ATPase, pIC50: ~6.5 |
99% | |||||||||||||||||
| Esomeprazole sodium | ✔ | 98% | |||||||||||||||||
| BTB06584 | ✔ | 99% | |||||||||||||||||
| Ciclopirox | ✔ | 97% | |||||||||||||||||
| CB-5083 |
++++
p97 AAA ATPase, IC50: 11 nM |
99%+ | |||||||||||||||||
| Ciclopirox olamine | ✔ | 99% | |||||||||||||||||
| Brefeldin A |
+++
ATPase (HCT 116), IC50: 0.2 μM |
99%+ | |||||||||||||||||
| Oligomycin A | ✔ | 99% | |||||||||||||||||
| Sodium orthovanadate |
+++
(Na,K)-ATPase, IC50: 40 nM |
25-28%V | |||||||||||||||||
| Golgicide A | ✔ | 99%+ | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | The importance of the Ca2+-ATPases of the surface and endoplasmic reticulum membranes in regulating the intracellular Ca2+ concentrations in living cells has been recognized as a result of the development of biophysical techniques and finding of useful pharmacological tool drugs[1]. BHQ is a potent and selective inhibitor of the sarco-endoplasmic reticulum Ca2+-ATPase (SERCA). In rat tail artery myocytes, BHQ reduced ICa(L) in a concentration- and voltage-dependent manner with an IC50 of 66.7 μM[2]. In rat basophilic leukaemia (RBL-2H3) cells under whole cell voltage clamp, a maximal blockade of inward current was obtained within 6 min after perfusion with 10 μM BHQ which caused depolarization of the cell which would affect Ca2+ influx[3]. |
| Concentration | Treated Time | Description | References | |
| Eremosphaera viridis | 10 µM | 2.9 ± 1.2 minutes | Inhibited the ER Ca2+-ATPase, thereby preventing Sr2+-induced repetitive [Ca2+]cy spikes | Plant Physiol. 1998 Jun;117(2):545-57. |
| HL60 cells | 0.31 µM, 0.63 µM, 1.25 µM | 48 hours | Evaluate the cytotoxicity of BHQ on HL60 cells, showing lower cytotoxicity for the parental cell line | Mol Pharm. 2013 Nov 4;10(11):4358-66. |
| HL60/MX2 cells | 0.31 µM, 0.63 µM, 1.25 µM | 48 hours | Evaluate the cytotoxicity of BHQ on HL60/MX2 cells, showing selective cytotoxicity for the resistant cell line (7.7 fold) | Mol Pharm. 2013 Nov 4;10(11):4358-66. |
| Mouse cardiomyocytes | 10 µM | Evaluate the effect of strong SERCA2a inhibition on Ca2+ alternans, showing significant reduction in Ca2+ transient amplitude and suppression of alternans | J Biol Chem. 2018 Aug 31;293(35):13650-13661. |
| Administration | Dosage | Frequency | Description | References | ||
| Caenorhabditis elegans | Ret-1(syb4955) mutant | Exposure in culture medium | 100 μM | Single dose, 4-hour exposure | Inhibition of ER/SR Ca2+ reuptake rescued key phenotypic differences in the mutant | Brain. 2024 Jul 5;147(7):2334-2343 |
| Mice | RyR2 WT and mutant Mice models | Perfusion | 3 μM and 10 μM | 5-14 Hz stimulation frequency | Evaluate the effect of tBHQ on Ca2+ alternans, showing minor impact with 3 μM tBHQ and significant suppression with 10 μM tBHQ | J Biol Chem. 2018 Aug 31;293(35):13650-13661. |
| Mice | RyR2 WT and RyR2 R4496C mutant mice | Perfusion | 3 μM and 10 μM | Electrical stimulation at various frequencies (5-14 Hz) | To evaluate the effect of tBHQ on Ca2+ alternans. 3 μM tBHQ had little impact on Ca2+ alternans, whereas 10 μM tBHQ markedly reduced the amplitude of Ca2+ transients and suppressed Ca2+ alternans. | J Biol Chem. 2018 Aug 31;293(35):13650-13661. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.50mL 0.90mL 0.45mL |
22.49mL 4.50mL 2.25mL |
44.98mL 9.00mL 4.50mL |
|
| CAS号 | 88-58-4 |
| 分子式 | C14H22O2 |
| 分子量 | 222.32 |
| SMILES Code | C1=C(O)C(=CC(=C1C(C)(C)C)O)C(C)(C)C |
| MDL No. | MFCD00008825 |
| 别名 | 2,5-二特丁基对苯二酚 ;BHQ |
| 运输 | 蓝冰 |
| InChI Key | JZODKRWQWUWGCD-UHFFFAOYSA-N |
| Pubchem ID | 2374 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, room temperature |
| 溶解方案 |
DMSO: 105 mg/mL(472.29 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的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
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