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CHEBI:191856 - helioxanthin

ChEBI IDCHEBI:191856
ChEBI Namehelioxanthin
Stars
DefinitionA furonaphthodioxole that is furo[3',4':6,7]naphtho[1,2-d][1,3]dioxol-7(9H)-one substituted by a 1,3-benzodioxol-5-yl group at posiiton 10. It is a inhibitor of HBV, HCV and HSV-1 viruses.
Last Modified16 May 2022
SubmitterAdnan
DownloadsMolfile
FormulaC20H12O6
Net Charge0
Average Mass348.310
Monoisotopic Mass348.06339
SMILESO=C1OCc2c1cc1ccc3c(c1c2-c1ccc2c(c1)OCO2)OCO3
InChIInChI=1S/C20H12O6/c21-20-12-5-10-2-4-15-19(26-9-24-15)18(10)17(13(12)7-22-20)11-1-3-14-16(6-11)25-8-23-14/h1-6H,7-9H2
InChIKeyJUBRYHUFFFYTGR-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Eleutherococcus divaricatus var. chiisanensis (ncbitaxon:96666) Root (BTO:0001188) PubMed (12392817) Species also known as Acanthopanax chiisanensis.
Taiwania cryptomerioides (ncbitaxon:50187) - PubMed (26464283)
Roles Classification
Biological Roles:
anti-HBV agent  An antiviral agent that destroys or inhibits the replication of the hepatitis B virus.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
helioxanthin (CHEBI:191856) has role anti-HBV agent (CHEBI:64951)
helioxanthin (CHEBI:191856) has role antineoplastic agent (CHEBI:35610)
helioxanthin (CHEBI:191856) has role plant metabolite (CHEBI:76924)
helioxanthin (CHEBI:191856) is a benzodioxoles (CHEBI:38298)
helioxanthin (CHEBI:191856) is a furonaphthodioxole (CHEBI:50307)
helioxanthin (CHEBI:191856) is a lignan (CHEBI:25036)
IUPAC Name 
10-(1,3-benzodioxol-5-yl)furo[3',4':6,7]naphtho[1,2-d][1,3]dioxol-7(9H)-one
Synonyms  Source
10-(2H-1,3-benzodioxol-5-yl)-2H-furo[3',4':6,7]naphtho[1,2-d][1,3]dioxol-7(9H)-oneIUPAC
HE-145ChEBI
10-(1,3-benzodioxol-5-yl)-9H-[2]benzofuro[6,5-g][1,3]benzodioxol-7-oneChEBI
Manual XrefsDatabases
C00007211KNApSAcK
154166ChemSpider
US6306899Patent
Registry NumbersSources
CAS:18920-47-3ChemIDplus
Citations