2750119-14-1

6PPD-quinone-d<sub>5</sub> Chemical Structure
2750119-14-1

Chemical Structure

6PPD-quinone-d5

  • CAS No.: 2750119-14-1
  • Formula:C18H17D5N2O2
  • Molecular Weight:303.41

IUPAC Name: 2-((4-methylpentan-2-yl)amino)-5-((phenyl-d5)amino)cyclohexa-2,5-diene-1,4-dione

InChIKey: UBMGKRIXKUIXFQ-UPKDRLQUSA-N

SMILES: O=C(C=C1NC(C)CC(C)C)C(NC2=C([2H])C([2H])=C([2H])C([2H])=C2[2H])=CC1=O

Biological Activity: 6PPD-quinone-d5 is the deuterium labeled 6PPD-quinone[1].

Cat. No. Product Name Purity Description Pricing
HY-152039S
6PPD-quinone-d5 99.89% 6PPD-quinone-d5 is the deuterium labeled 6PPD-quinone.
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HY-153169R
6PPD-Q (Standard) ≥98% 6PPD-Q (Standard) is the analytical standard of 6PPD-Q (HY-153169). This product is intended for research and analytical applications. 6PPD-Q (6PPD-Quinone) is an environmental pollutant that can be detected in human urine and is widely present in the environment. 6PPD-Q targets and binds to CNR2, CNR1, AA2AR, LCAT, and TRPA1, with CNR2 exhibiting the highest binding affinity, potentially acting as a CNR2 receptor agonist to activate cannabinoid receptors. 6PPD-Q induces intestinal inflammation and barrier damage by disrupting mitochondrial function, reducing neuronal glycolysis metabolites and TCA cycle intermediates, and exacerbating α-synuclein (α-syn) aggregation. 6PPD-Q is applicable in research on environmental toxicology, neurodegenerative diseases, and inflammation-related disorders.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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HY-152039S1
6PPD-Q-13C6 98.0% 6PPD-quinone-13C6 is the 13C labeled 6PPD-quinone.
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This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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HY-153169
6PPD-Q 99.77% 6PPD-Q (6PPD-Quinone) is an environmental pollutant that can be detected in human urine and is widely present in the environment. 6PPD-Q targets and binds to CNR2, CNR1, AA2AR, LCAT, and TRPA1, with CNR2 exhibiting the highest binding affinity, potentially acting as a CNR2 receptor agonist to activate cannabinoid receptors. 6PPD-Q induces intestinal inflammation and barrier damage by disrupting mitochondrial function, reducing neuronal glycolysis metabolites and TCA cycle intermediates, and exacerbating α-synuclein (α-syn) aggregation. 6PPD-Q is applicable in research on environmental toxicology, neurodegenerative diseases, and inflammation-related disorders.
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Amount:

USD 0.00

This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

Pricing 
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References