Phenyl-p-benzoquinone

Cat. No. M11216

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

Synonym:

2-Phenyl-1,4-benzoquinone

Size	Price	Availability	Quantity
500mg	USD 90 USD90	In stock
1g	USD 120 USD120	In stock

Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation

Purity: >99%
COA
MSDS

Product Information

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

Related Products
O-acetylcamptothecin O-acetylcamptothecin is a derivative of camptothecin, a naturally occurring alkaloid extracted from the bark of the Chinese tree Camptotheca acuminata. Camptothecin and its derivatives are primarily known for their potent anticancer properties, particularly through their action as inhibitors of topoisomerase I, an enzyme critical for DNA replication and transcription.
10-hydroxystearic acid 10-hydroxystearic acid is a hydroxy fatty acid.
SB-T-1214 SB-T-1214 is a new-generation taxoid. SB-T-1214 possesses significant activity against colon cancer spheroids induced by and enriched with drug resistant tumorigenic CD133high/CD44high cells and efficiently inhibited expression of the majority of stem cell-related genes.
NG-497 NG-497 is a selective human adipose triglyceride lipase (ATGL) inhibitor that targets the enzymatically active patatin-like domain of human ATGL.
PCL-PEG-MAL PCL-PEG-MAL is an amphiphilic block copolymer consisting of polycaprolactone (PCL), polyethylene glycol (PEG) and maleimide (MAL) functional groups. PCL-PEG-MAL is used in targeted delivery systems, surface modification of nanomaterials, functionalisation of biomaterials and biosensing technologies for specific chemical linkages or biomolecular immobilisation.

Catalog

By Signaling Pathways

By Product Type

Signaling Pathways

Phenyl-p-benzoquinone

2-Phenyl-1,4-benzoquinone

Quality Control & Documentation

Biological Activity

Chemical Information

References

Get to Know Us

Customer Support

Resources

Contact Us