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Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O4
Molecular Weight 168.1467
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,6-DIMETHOXYQUINONE

SMILES

COC1=CC(=O)C=C(OC)C1=O

InChI

InChIKey=OLBNOBQOQZRLMP-UHFFFAOYSA-N
InChI=1S/C8H8O4/c1-11-6-3-5(9)4-7(12-2)8(6)10/h3-4H,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H8O4
Molecular Weight 168.1467
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Occupational allergic contact dermatitis caused by wood dusts.
2001 Apr
Phytochemical constituents of Artemisia stolonifera.
2001 Aug
Quinone oxidoreductase message levels are differentially regulated in parasitic and non-parasitic plants exposed to allelopathic quinones.
2001 Feb
Differential RNA expression of alpha-expansin gene family members in the parasitic angiosperm Triphysaria versicolor (Scrophulariaceae).
2001 Mar 21
Wheat germ extract inhibits experimental colon carcinogenesis in F-344 rats.
2001 Oct
Transcriptional responses in the hemiparasitic plant Triphysaria versicolor to host plant signals.
2001 Sep
Antiplatelet and anti-inflammatory constituents and new oxygenated xanthones from Hypericum geminiflorum.
2002 Jan
Cytotoxic constituents of the stem bark of Neolitsea acuminatissima.
2002 Mar
A novel and efficient chiral palladium-phosphinooxazolidine catalyst for the enantioselective Diels-Alder reaction.
2002 May 21
Dehydrogenation of aromatic amines to imines via ruthenium-catalyzed hydrogen transfer.
2002 May 21
Anti-platelet aggregation and chemical constituents from the rhizome of Gynura japonica.
2003 Aug
A medical nutriment has supportive value in the treatment of colorectal cancer.
2003 Aug 4
New lignans and cytotoxic constituents from Wikstroemia lanceolata.
2004 Mar
Pscroph, a parasitic plant EST database enriched for parasite associated transcripts.
2005 Nov 16
Secondary metabolites from the wood bark of Durio zibethinus and Durio kutejensis.
2006 Aug
Antibacterial evaluation of 1,4-benzoquinone derivatives.
2006 Mar 22
[Studies on chemical constituents from Serissa serissoides].
2007 Apr
alpha-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae).
2007 Mar
Safety studies regarding a standardized extract of fermented wheat germ.
2007 May-Jun
Photophysical properties of quinones and their interaction with the photosynthetic reaction centre.
2008 Aug
Cotton benzoquinone reductase: up-regulation during early fiber development and heterologous expression and characterization in Pichia pastoris.
2008 Aug-Sep
[Chemical constituents of aerial part of Acalypha australis].
2008 Jun
Cloning and characterization of a new laccase from Bacillus licheniformis catalyzing dimerization of phenolic acids.
2008 May
Improving the functional expression of a Bacillus licheniformis laccase by random and site-directed mutagenesis.
2009 Feb 23
Quinone-enhanced reduction of nitric oxide by xanthine/xanthine oxidase.
2009 May
Structure-function studies of a Melanocarpus albomyces laccase suggest a pathway for oxidation of phenolic compounds.
2009 Oct 2
Minor secondary metabolic products from the stem bark of Plumeria rubra Linn. displaying antimicrobial activities.
2010 Apr
Antimicrobial activities of 1,4-benzoquinones and wheat germ extract.
2010 Aug
Oxidation of atenolol, propranolol, carbamazepine and clofibric acid by a biological Fenton-like system mediated by the white-rot fungus Trametes versicolor.
2010 Jan
Oxidative depolymerization of lignin in ionic liquids.
2010 Jun 21
Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione.
2010 Nov 15
Differential regulation of laccase gene expression in Coriolopsis rigida LPSC No. 232.
2010 Nov-Dec
Advanced oxidation of benzene, toluene, ethylbenzene and xylene isomers (BTEX) by Trametes versicolor.
2010 Sep 15
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:02:20 GMT 2023
Edited
by admin
on Fri Dec 15 19:02:20 GMT 2023
Record UNII
1Z701W789S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-DIMETHOXYQUINONE
MI  
Common Name English
2,6-DIMETHOXY-1,4-BENZOQUINONE
Systematic Name English
2,6-DIMETHOXY-2,5-CYCLOHEXADIENE-1,4-DIONE
Systematic Name English
2,6-DIMETHOXYQUINONE [MI]
Common Name English
NSC-56336
Code English
NSC-24500
Code English
2,6-DIMETHOXYBENZOQUINONE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C796
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
Code System Code Type Description
WIKIPEDIA
2,6-DIMETHOXYBENZOQUINONE
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
MESH
C030511
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
CAS
530-55-2
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
FDA UNII
1Z701W789S
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-484-7
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
MERCK INDEX
m4516
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY Merck Index
NSC
24500
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
NCI_THESAURUS
C126754
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY NCIT
EPA CompTox
DTXSID80862128
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
PUBCHEM
68262
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
NSC
56336
Created by admin on Fri Dec 15 19:02:20 GMT 2023 , Edited by admin on Fri Dec 15 19:02:20 GMT 2023
PRIMARY
Related Record Type Details
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