ChEBI Name coenzyme Q10
ChEBI ID CHEBI:46245
ChEBI ASCII Name coenzyme Q10
Definition A ubiquinone having a side chain of 10 isoprenoid units. In the naturally occurring isomer, all isoprenyl double bonds are in the E- configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:9854, CHEBI:46241
Supplier Information
Save molfile Download Molfile
more structures >>
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C59H90O4
Net Charge 0
Average Mass 863.34350
Monoisotopic Mass 862.684
InChI InChI=1S/C59H90O4/c1-44(2)24-15-25-45(3)26-16-27-46(4)28-17-29-47(5)30-18-31-48(6)32-19-33-49(7)34-20-35-50(8)36-21-37-51(9)38-22-39-52(10)40-23-41-53(11)42-43-55-54(12)56(60)58(62-13)59(63-14)57(55)61/h24,26,28,30,32,34,36,38,40,42H,15-23,25,27,29,31,33,35,37,39,41,43H2,1-14H3/b45-26+,46-28+,47-30+,48-32+,49-34+,50-36+,51-38+,52-40+,53-42+
InChIKey ACTIUHUUMQJHFO-UPTCCGCDSA-N
SMILES COC1=C(OC)C(=O)C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)=C(C)C1=O
Metabolite of Species Details
Homo sapiens (NCBI:9606) See: DOI
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via ubiquinones )
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via ubiquinones )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing coenzyme Q10 (CHEBI:46245) has role antioxidant (CHEBI:22586)
coenzyme Q10 (CHEBI:46245) has role human metabolite (CHEBI:77746)
coenzyme Q10 (CHEBI:46245) is a ubiquinones (CHEBI:16389)
IUPAC Name
2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-yl]-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
Synonyms Sources
2-((all-E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl-p-benzoquinone ChemIDplus
2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-yl]-5,6-dimethoxy-3-methyl-1,4-benzoquinone ChEBI
Adelir KEGG DRUG
all-trans-ubiquinone ChEBI
coenzyme Q10 ChemIDplus
Coenzyme Q10 KEGG COMPOUND
CoQ ChEBI
CoQ10 ChEBI
Q ChEBI
Q 199 ChemIDplus
Q10 ChEBI
Ubidecarenone KEGG COMPOUND
ubiquinone ChEBI
ubiquinone 10 ChemIDplus
ubiquinone 50 ChemIDplus
UBIQUINONE-10 PDBeChem
Ubiquinone-10 KEGG COMPOUND
Database Links Databases
C00002866 KNApSAcK
C11378 KEGG COMPOUND
Coenzyme_Q10 Wikipedia
D01065 KEGG DRUG
HMDB01072 HMDB
LMPR02010001 LIPID MAPS
U10 PDBeChem
View more database links
Registry Numbers Types Sources
1900141 Beilstein Registry Number Beilstein
1900141 Reaxys Registry Number Reaxys
303-98-0 CAS Registry Number KEGG COMPOUND
303-98-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10953455 PubMed citation Europe PMC
13445756 PubMed citation Europe PMC
17192765 PubMed citation Europe PMC
17605305 PubMed citation Europe PMC
18787645 PubMed citation Europe PMC
18843432 PubMed citation Europe PMC
20367194 PubMed citation Europe PMC
25544601 PubMed citation Europe PMC
26741866 PubMed citation Europe PMC
27012265 PubMed citation Europe PMC
7599208 PubMed citation Europe PMC
7718355 PubMed citation Europe PMC
Last Modified
18 julio 2016
General Comment
2010-04-29 Additional citation (no PMID) -- Kawahara K et al., (1994): Isolation of Sphingomonas Strains from Ears of Rice and Other Plants of Family Gramineae - Biosci. Biotech. Biochem. 58(3): 600-601.