helioxanthin (CHEBI:191856)

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ChEBI Name	helioxanthin

ChEBI ID	CHEBI:191856

Definition	A 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.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

Formula

C20H12O6

Net Charge

Average Mass

348.310

Monoisotopic Mass

348.06339

InChI

InChI=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

InChIKey

JUBRYHUFFFYTGR-UHFFFAOYSA-N

SMILES

O=C1OCC2=C(C3=CC4=C(OCO4)C=C3)C3=C(C=CC4=C3OCO4)C=C12

Metabolite of Species	Details
Taiwania cryptomerioides (NCBI:txid50187)	See: PubMed
Eleutherococcus divaricatus var. chiisanensis (NCBI:txid96666)	Found in Root (BTO:0001188). Species also known as Acanthopanax chiisanensis. See: PubMed

Roles Classification
Biological Role(s):	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(s):	antineoplastic agent A substance that inhibits or prevents the proliferation of neoplasms.

ChEBI Ontology
Outgoing	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	Sources
10-(1,3-benzodioxol-5-yl)-9H-[2]benzofuro[6,5-g][1,3]benzodioxol-7-one	ChEBI
10-(2H-1,3-benzodioxol-5-yl)-2H-furo[3',4':6,7]naphtho[1,2-d][1,3]dioxol-7(9H)-one	IUPAC
HE-145	ChEBI

Registry Number	Type	Source
18920-47-3	CAS Registry Number	ChemIDplus

Last Modified

16 May 2022