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Phenyl-p-benzoquinone

Cat. No. M11216

All AbMole products are for research use only, cannot be used for human consumption.

Phenyl-p-benzoquinone Structure
Synonym:

2-Phenyl-1,4-benzoquinone

Size Price Availability Quantity
500mg USD 90  USD90 In stock
1g USD 120  USD120 In stock
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Quality Control & Documentation
Biological Activity

Phenyl-p-benzoquinone (PBQ; 2-Phenyl-1,4-benzoquinone) stimulus trigger a different peripheral cytokine cascade compared to acetic acid, it induces writhing response dependent on IL-18, IFNγ and endothelin-1.

Chemical Information
Molecular Weight 184.19
Formula C12H8O2
CAS Number 363-03-1
Solubility (25°C) DMSO
Storage 2-8°C, dry, sealed
References

[1] Sai Das, et al. J Photochem Photobiol B . PSII as an in vivo molecular catalyst for the production of energy rich hydroquinones - A new approach in renewable energy

[2] Gabriela F Pavao-de-Souza, et al. Pharmacol Biochem Behav . Acetic acid- and phenyl-p-benzoquinone-induced overt pain-like behavior depends on spinal activation of MAP kinases, PI(3)K and microglia in mice

[3] A Freyberger, et al. Arch Toxicol . Inhibition of prostaglandin-H-synthase by o-phenylphenol and its metabolites

[4] H Sato, et al. Cancer Lett . Effects of 2-phenyl-1,4-benzoquinone and 2,5-dihydroxybiphenyl on two-stage mouse skin carcinogenesis

[5] Michael Emmanuel Mutseyekwa, et al. Water Sci Technol. Ozonation for the removal of bisphenol A

[6] Renata M Martinez, et al. Scientifica (Cairo). Antinociceptive Effect of Tephrosia sinapou Extract in the Acetic Acid, Phenyl-p-benzoquinone, Formalin, and Complete Freund's Adjuvant Models of Overt Pain-Like Behavior in Mice

[7] Gabriela F Pavao-de-Souza, et al. Pharmacol Biochem Behav. Acetic acid- and phenyl-p-benzoquinone-induced overt pain-like behavior depends on spinal activation of MAP kinases, PI(3)K and microglia in mice

[8] C R Fernando, et al. J Med Chem. Studies on the mechanism of toxicity of acetaminophen. Synthesis and reactions of N-acetyl-2,6-dimethyl- and N-acetyl-3,5-dimethyl-p-benzoquinone imines

[9] J Esteve, et al. Gen Pharmacol. Pharmacological profile of droxicam

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Keywords: Phenyl-p-benzoquinone, 2-Phenyl-1,4-benzoquinone supplier, inhibitors, activators

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