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CHEBI:46245 - coenzyme Q10

ChEBI IDCHEBI:46245
ChEBI Namecoenzyme Q10
Stars
ASCII Namecoenzyme Q10
DefinitionA ubiquinone having a side chain of 10 isoprenoid units. In the naturally occurring isomer, all isoprenyl double bonds are in the E- configuration.
Secondary ChEBI IDsCHEBI:9854, CHEBI:46241
Last Modified26 May 2021
DownloadsMolfile
FormulaC59H90O4
Net Charge0
Average Mass863.365
Monoisotopic Mass862.68391
SMILESCOC1=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
InChIInChI=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+
InChIKeyACTIUHUUMQJHFO-UPTCCGCDSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606) - DOI (10.1038/nbt.2488)
Roles Classification
Chemical Role:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Roles:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
ferroptosis inhibitor  Any substance that inhibits the process of ferroptosis (a type of programmed cell death dependent on iron and characterized by the accumulation of lipid peroxides) in organisms.
Escherichia coli metabolite  Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
ChEBI Ontology
Outgoing Relation(s)
coenzyme Q10 (CHEBI:46245) has role antioxidant (CHEBI:22586)
coenzyme Q10 (CHEBI:46245) has role ferroptosis inhibitor (CHEBI:173084)
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  Source
Ubiquinone-10KEGG COMPOUND
UbidecarenoneKEGG COMPOUND
coenzyme Q10ChemIDplus
ubiquinone 50ChemIDplus
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-benzoquinoneChemIDplus
ubiquinone 10ChemIDplus
UniProt Name  Source
ubiquinone-10UniProt
Manual XrefsDatabases
C11378KEGG COMPOUND
D01065KEGG DRUG
U10PDBeChem
LMPR02010001LIPID MAPS
Coenzyme_Q10Wikipedia
HMDB0001072HMDB
C00002866KNApSAcK
UBIQUINONE-10MetaCyc
4607DrugCentral
4445197ChemSpider
FDB013228FooDB
Registry NumbersSources
Beilstein:1900141Beilstein
Reaxys:1900141Reaxys
CAS:303-98-0NIST Chemistry WebBook
CAS:303-98-0ChemIDplus
Citations