Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H6O2 |
| Molecular Weight | 182.1748 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1C(=O)C2=C3C1=CC=CC3=CC=C2
InChI
InChIKey=AFPRJLBZLPBTPZ-UHFFFAOYSA-N
InChI=1S/C12H6O2/c13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(11)14/h1-6H
| Molecular Formula | C12H6O2 |
| Molecular Weight | 182.1748 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Activation of 5-lipoxygenase and NF-kappa B in the action of acenaphthenequinone by modulation of oxidative stress. | 2008-01 |
|
| Characterization of an oligomeric carbonyl reductase of dog liver: its identity with peroxisomal tetrameric carbonyl reductase. | 2007-09 |
|
| An environmental quinoid polycyclic aromatic hydrocarbon, acenaphthenequinone, modulates cyclooxygenase-2 expression through reactive oxygen species generation and nuclear factor kappa B activation in A549 cells. | 2007-02 |
|
| Enzymatic properties of a member (AKR1C20) of the aldo-keto reductase family. | 2006-03 |
|
| The specificity of cross-reactivity: promiscuous antibody binding involves specific hydrogen bonds rather than nonspecific hydrophobic stickiness. | 2003-10 |
|
| Antibody multispecificity mediated by conformational diversity. | 2003-02-28 |
|
| Oxidation of naphthenoaromatic and methyl-substituted aromatic compounds by naphthalene 1,2-dioxygenase. | 1996-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:10:12 GMT 2025
by
admin
on
Mon Mar 31 21:10:12 GMT 2025
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| Record UNII |
3950D6UEIQ
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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7656
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82-86-0
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2660
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6724
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3950D6UEIQ
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15342
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Acenaphthoquinone
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C023722
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DTXSID7049429
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