Chemical Name: 1,4-Dihydroxy-2,5-di-tert-butylbenzene
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
A selective inhibitor of endoplasmic reticulum Ca2+-ATPase.
Technical Data
M. Wt
222.33
Formula
C14H22O2
Storage
Store at RT
CAS Number
88-58-4
PubChem ID
2374
InChI Key
JZODKRWQWUWGCD-UHFFFAOYSA-N
Smiles
CC(C)(C)C1=CC(O)=C(C=C1O)C(C)(C)C
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solubility
Soluble to 100 mM in DMSO
Preparing Stock Solutions
The following data is based on the product molecular weight 222.33. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
4.5 mL
22.49 mL
44.98 mL
5 mM
0.9 mL
4.5 mL
9 mL
10 mM
0.45 mL
2.25 mL
4.5 mL
50 mM
0.09 mL
0.45 mL
0.9 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Dettbarn and Palade
(1999) Effects of three sarcoplasmic/endoplasmic Ca++ pump inhibitors on release channels and intracellular stores. J.Pharmacol.Exp.Ther. 285 739 PMID: 9580621
Fusiet al (1999) 2,5-Di-t-butyl-1,4 benzohydroquinone induces endothelium-dependent relaxation of rat thoracic aorta. Eur.J.Pharmacol. 366 181 PMID: 10082199
Hassessianet al (1994) Blockade of the inward rectifier potassium current by the Ca2+-ATPase inhibitor 2',5'-di(tert-butyl)-1,4-benzohydroquinone (BHQ). Br.J.Pharmacol. 112 1118 PMID: 7952872
Janet al (1999) Mechanism of rise and decay of 2,5-di-tert-butylhydroquinone-induced Ca2+ signals in Madin Darby canine kidney cells. Eur.J.Pharmacol. 365 111 PMID: 9988129