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CHEBI:138077 - chloroxanthin

ChEBI IDCHEBI:138077
ChEBI Namechloroxanthin
Stars
DefinitionA carotenol obtained by formal hydration across the double bonds at position 1 of neurosporene.
Secondary ChEBI IDCHEBI:80158
Last Modified8 January 2021
SubmitterAnne Morgat
DownloadsMolfile
FormulaC40H60O
Net Charge0
Average Mass556.919
Monoisotopic Mass556.46442
SMILESCC(C)=CCC/C(C)=C/CC/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C=C(\C)CCCC(C)(C)O
InChIInChI=1S/C40H60O/c1-33(2)19-13-22-36(5)25-16-28-37(6)26-14-23-34(3)20-11-12-21-35(4)24-15-27-38(7)29-17-30-39(8)31-18-32-40(9,10)41/h11-12,14-15,17,19-21,23-27,29-30,41H,13,16,18,22,28,31-32H2,1-10H3/b12-11+,23-14+,24-15+,29-17+,34-20+,35-21+,36-25+,37-26+,38-27+,39-30+
InChIKeyIWZRTQIXVDXLNL-PZKADDIDSA-N
Species of MetaboliteComponentSourceComments
Rhodobacter sphaeroides (ncbitaxon:633146) - PubMed (17609942) Strain: GA
Rhodovulum sulfidophilum (ncbitaxon:35806) - PubMed (17107420)
Myxococcus xanthus (ncbitaxon:34) - PubMed (Eur.J.Biochem, 233, (1995), 238)
Roles Classification
Biological Role:
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
ChEBI Ontology
Outgoing Relation(s)
chloroxanthin (CHEBI:138077) has functional parent neurosporene (CHEBI:16833)
chloroxanthin (CHEBI:138077) has role bacterial metabolite (CHEBI:76969)
chloroxanthin (CHEBI:138077) is a carotenol (CHEBI:23045)
chloroxanthin (CHEBI:138077) is a tertiary alcohol (CHEBI:26878)
IUPAC Name 
1,2,7',8'-tetrahydro-ψ,ψ-caroten-1-ol
Synonyms  Source
HydroxyneurosporeneKEGG COMPOUND
1-hydroxy-all-trans-1,2-dihydroneurosporeneSUBMITTER
1-hydroxy-1,2-dihydroneurosporeneSUBMITTER
1-hydroxyneurosporeneMetaCyc
OH-NeurosporeneLIPID MAPS
(6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,14,16,18,20,22,26,30-undecaen-2-olIUPAC
UniProt Name  Source
1-hydroxy-all-trans-1,2-dihydro-neurosporeneUniProt
Manual XrefsDatabases
C00000927KNApSAcK
C15892KEGG COMPOUND
CPD-11463MetaCyc
LMPR01070113LIPID MAPS
Registry NumbersSources
CAS:2104-74-7KNApSAcK
Citations