Record Information Version 1.0 Status Detected and Quantified Creation Date 2022-05-16 21:37:40 UTC Update Date 2022-09-01 02:26:39 UTC MiMeDB ID MMDBc0053888 Metabolite Identification Common Name Ubiquinol-0 Description 2,3-Dimethoxy-5-methylhydroquinone, also known as ubiquinol 7 or coenzyme Q0 reduced form, belongs to the class of organic compounds known as ubiquinols. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methylbenzene-1,4-diol moiety to which an isoprenyl group is attached at ring position 2(or 6). Based on a literature review a small amount of articles have been published on 2,3-Dimethoxy-5-methylhydroquinone. Structure Synonyms Value Source 2,3-Dimethoxy-5-methyl-1,4-benzoquinol ChEBI 2,3-Dimethoxy-5-methyl-1,4-dihydroxybenzene ChEBI Coenzyme Q0 reduced form ChEBI Ubiquinol 7 HMDB Ubiquinol 6 (ubiquinol 30) HMDB Ubiquinol 9 HMDB Ubiquinol HMDB Ubiquinol 0 HMDB Ubiquinol 1 HMDB Ubiquinol 50 HMDB Ubiquinols HMDB Ubiquinone hydroquinone HMDB 2,3-Dimethoxy-5-methylhydroquinone ChEBI
Chemical Formula C9 H12 O4 Average Molecular Weight 184.191 Monoisotopic Molecular Weight 184.073558866 IUPAC Name Not Available Traditional Name Not Available CAS Registry Number Not Available SMILES Not Available InChI Identifier InChI=1S/C9H12O4/c1-5-4-6(10)8(12-2)9(13-3)7(5)11/h4,10-11H,1-3H3
InChI Key DSBZYDDWLLIJJS-UHFFFAOYSA-N Chemical Taxonomy Description Belongs to the class of organic compounds known as ubiquinols. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methylbenzene-1,4-diol moiety to which an isoprenyl group is attached at ring position 2(or 6). Kingdom Organic compounds Super Class Lipids and lipid-like molecules Class Prenol lipids Sub Class Quinone and hydroquinone lipids Direct Parent Ubiquinols Alternative Parents Substituents Ubiquinol skeleton
Methoxyphenol
Dimethoxybenzene
O-dimethoxybenzene
Anisole
Hydroquinone
M-cresol
Phenoxy compound
O-cresol
Phenol ether
Methoxybenzene
Alkyl aryl ether
Phenol
Toluene
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Ether
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound Molecular Framework Aromatic homomonocyclic compounds External Descriptors Functional Ontology Not Available Physical Properties State Expected Solid Predicted Properties Not Available Spectra Not Available Biological Properties Cellular Locations Not Available Biospecimen Locations Not Available Tissue Locations Not Available Associated OMIM IDs 114500 (Colorectal cancer)610247 (Eosinophilic esophagitis)Human Proteins and Enzymes Proteins Human Pathways Pathways Metabolic Reactions Reaction ID Precursor Product Enzyme Reaction Type Data Source Reference
Health Effects and Bioactivity Health Outcome/Bioactivity Metabolite Response/Effect Related Health Condition Evidence Type Measured in Matrix Data Source Reference
Microbial Sources Kingdom Phylum Total species Hosts and Body Sites Microbial Links
Exposure Sources Source Type Source Sub-type Species Data Source Reference Details
Host Biospecimen and Location Host and Biospecimen Status Mean Std Min Max Units Age Sex Health Condition Data Source Reference
External Links HMDB ID HMDB0246128 DrugBank ID Not Available Phenol Explorer Compound ID Not Available FooDB ID Not Available KNApSAcK ID Not Available Chemspider ID 9358112 KEGG Compound ID Not Available BioCyc ID Not Available BiGG ID Not Available Wikipedia Link Not Available METLIN ID Not Available PubChem Compound 11183027 PDB ID Not Available ChEBI ID 60899 Food Biomarker Ontology Not Available References Synthesis Reference Not Available General References Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]
